Next Article in Journal
Fight, Not Flight! Avoidant Goals Strengthen Attentional Biases During Increased Anxiety in Healthy Adults
Previous Article in Journal
Validity of the Greek Knowledge About Childhood Autism Among Health Workers (KCAHW) Questionnaire
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Insight and Violence: An Overview of the Possible Link and Treatment Options in Forensic Psychiatric Settings

by
Bianca-Mălina Horgoș
1,
Daniel Ungureanu
2,3,* and
Cătălina-Angela Crișan
1,4
1
First Psychiatric Clinic, Emergency County Hospital, 43 Victor Babeș Street, 400012 Cluj-Napoca, Romania
2
Department Pharmacy I, Discipline of Pharmaceutical Chemistry, “Iuliu Hațieganu” University of Medicine and Pharmacy, 41 Victor Babeș Street, 400012 Cluj-Napoca, Romania
3
“Prof. Dr. Ion Chiricuță” Oncology Institute, 34-36 Republicii Street, 400015 Cluj-Napoca, Romania
4
Department of Neurosciences, Discipline of Psychiatry and Pediatric Psychiatry, “Iuliu Hațieganu” University of Medicine and Pharmacy, 43 Victor Babeș Street, 400012 Cluj-Napoca, Romania
*
Author to whom correspondence should be addressed.
Psychiatry Int. 2024, 5(4), 975-998; https://doi.org/10.3390/psychiatryint5040067
Submission received: 25 September 2024 / Revised: 9 November 2024 / Accepted: 2 December 2024 / Published: 6 December 2024

Abstract

:
The belief that people suffering from psychiatric disorders are more violent, in particular psychotic patients that do not have insight into their illness, is very common in the general population. Therefore, this review aimed to present a more accurate depiction of the link between lack of insight and violent behavior, by evaluating the existing scientific literature on the topic. For this purpose, a literature search on PubMed, Embase, and Google Scholar was conducted, selecting the relevant papers published during a 20-year period (2004–2024). The paper defined insight as a multi-dimensional concept and discussed its classification, explanatory models, and clinical implications, followed by a presentation of several insight-measuring scales. The meaning of violent behavior, its prevalence, underlying mechanisms, and different measuring scales were discussed, followed by the confounding factors that influence the relationship between insight and violent behavior, treatment options for violence in forensic psychiatry settings, and methods to improve medication adherence. Contrasting results were observed regarding the impact of each factor on leading to violent acts, which suggested that the relationship between insight and violence is more complex than previously thought. In conclusion, increased attention must be paid to the investigated dimensions of both the concepts and the confounding factors, with further research required on this topic.

1. Introduction

The concept of insight was first described in the beginning of the nineteenth century when medical records first started to include observations regarding the patients’ awareness about their medical conditions. At the end of the same century, the term started to reflect the awareness of mental illness and has become an important instrument in establishing the prognosis of a psychiatric disorder, in particular schizophrenia and bipolar affective disorder [1,2,3].
Lack of insight is a prominent feature in patients with schizophrenia, with a staggering proportion between 50% and 80% of them not believing they have a disorder. Therefore, managing the disorder becomes a challenge for both the medical team and the patients, due to decreased medication adherence, increased hospitalization rates, and hostility, which can degenerate into violent acts. According to a study conducted by Fazel et al. during a period of 15.6 years, 40% of the patients were violently offended after discharge and the mean time to violent crime was 4.2 years. Consequently, violent acts can be directed toward anyone around the patient, including medical staff. This was reflected in a study conducted by Broderick et al.; in a multihospital state psychiatric system over two years, 31.4% of the patients committed at least one violent act, with a higher prevalence against other patients than against the medical staff [4,5,6,7,8].
In this regard, the impact of no insight in psychiatric patients that commit violent offences is significant, since violence in this population is a subject of forensic psychiatric expertise and the legal consequences of such acts often lead to guardianship, mandatory hospitalization, and mandatory treatment [9,10].
With this in mind, our quest on this subject began in the context of the popular belief that people suffering from mental illness, specifically psychotic disorders, present an increased risk of exhibiting violent behavior. Moreover, it is a constant debate if patients suffering from psychosis who have no or little understanding of their illness and symptoms (named poor insight) have an increased risk of violence. Starting our documentation with Amador and Davis’s Insight & Psychosis [11], we learned that this dilemma is far from new. Arango et al. (1999) stated that poor insight is the best predictor for violent behavior. Later, Friedman et al. (2003) observed that violent patients presented more positive symptoms and less insight. At the same time, other authors, like Trauer and Sacks (2000) and Kamali et al. (2001), pointed out that there is a strong correlation between insight and violent behavior but only after exclusion of the influence of substance abuse [12,13,14,15].
However, although several studies touched on this subject, it is difficult to track consistent results because of the different definitions, scales, and protocols used. An important problem resides in the understanding and quantification of insight and in the broad definition of “violent behavior”. In the present study, we aimed to clarify the concept of insight, its existing methods of assessment and clinical implications, and to present the current situation regarding aggression in the psychiatric population in order to discuss the relationship between the two, based on existing literature. We also aimed to present pharmacological and non-pharmacological interventions for violent patients in forensic psychiatry settings and possible options to increase medication adherence.

2. Material and Methods

To establish a potential relationship between lack of insight and violence, we conducted a literature search on PubMed, Embase, and Google Scholar databases using the following search terms: violence, violent behavior, insight, schizophrenia, psychiatric patient, bipolar disorder, and psychosis. We investigated the studies published in the last two decades (2004–2023), available in English, with participants at least 18 years old with a diagnosis of schizophrenia spectrum disorder, bipolar disorder, or first-episode psychosis, according to the DSM or ICD criteria. Studies not relevant to the topic and pediatric studies were excluded. The literature search also included manually selected references of narrative reviews, systematic reviews, and meta-analyses.

3. What Is Insight?

After the first descriptions of schizophrenia and psychosis came the questions regarding patients’ understanding of their illness, and with that the first definitions of the concept, which dated from the early nineteenth century. The pioneers of this concept were Jaspers, who distinguished between awareness of illness and insight in his book General Psychopathology [16], and Sir Aubrey Lewis, who first provided a temporary definition of the term as “A correct attitude to morbid change in oneself” in 1934. Many other definitions have followed. Gestalt psychologists named insight “the sudden appreciation of how parts are related to an organized whole with the accompanying <<aha>> experience” (Harre and Lamb, 1983) [17].
The New Oxford Textbook of Psychiatry, third edition, defined insight as “a patient’s capacity to understand the nature, significance, and severity of his or her illness” [18]. From an Explanatory Model perspective, insight in psychosis is the degree of congruence between patient and physician viewpoints [19].
Considering that insight is a multidimensional concept, a linear definition could not comprise all of the aspects of the term; thus, more comprehensive descriptions and classifications have been formulated. Perhaps the most well-known description is that of David from 1990 [11], which included the following: (1) the recognition of the mental illness, (2) compliance with treatment and (3) the ability to label unusual events as pathological. However, many other dimensions have been studied, with the study of Markova from 2005 being the most extensive found in our research [20]. This included nine components, as follows: (1) an attribution of the change to pathology, (2) social consequences of illness, (3) views concerning etiology and likely recurrence, (4) perception of changes in self and one’s interaction with the world, (5) need for medical treatment, (6) attitudes towards experiences, (7) comparisons with previous function, (8) predictions/postdictions of performance on specific tests, and (9) resemblance of own experiences to hypothetical cases.
Researchers have traditionally divided insight into two concepts: clinical insight, defined as the awareness of a mental illness requiring treatment, and cognitive insight, defined as the ability to re-evaluate thoughts and beliefs and to resist self-certainty [21]. Cognitive insight is evaluated with regards to two sub-components: self-reflectivity, or the ability to change one’s beliefs about itself, and self-certainty, meaning the confidence in being right, which implies resistance to feedback from others [22]. Metacognitive insight is a relatively new concept and was described by Spalletta et al. to be the most accurate form of one’s judgement about the self. As the name “metacognitive” implies, this term refers to thinking about one’s thinking, meaning the person’s self-awareness of their cognitive processes or the ability to self-monitor one’s changes in their state of mind and sensations [23].
Between 50–80% of people with schizophrenia spectrum disorder have no or little insight into their illness [24]. The rates are more encouraging for bipolar disorder, with 30% of patients having impaired insight [25].

4. Explanatory Models of Insight

Ever since the first depictions of this concept, researchers have struggled to determine the nature and etiology of insight. Many explanatory models have been formulated, none of them being able to fully explain the extensiveness of the subject. In their review from 2010, Chakraborty and Basu [17] synthesized the etiological models into the following: (A) insight as a positive symptom, considering the absence of insight a “delusion of health” [26]; (B) insight as a negative symptom, explained by the “mental withdrawal” from attempting to understand one’s own perception of the world [27]; (C) insight as a disorganized symptom, associated with the formal thought disorder often seen in schizophrenia; (D) insight as a defense mechanism, considering that patients use denial to protect themselves against the potentially devastating realization of a own’s mental illness; (E) lack of insight as misattribution, referring to the attribution of their symptoms to an external force (evil spirits, punishment by God, black magic, etc.) [28]; (F) insight as impaired metarepresentation, as patients appeared to be more able to recognize pathologic symptoms when “another person’s symptoms” and not their own [29]; (G) individual models of insight, considering individual’s values and beliefs in their understanding of the disorder; (H) insight as a sociocultural process, since people can have various culturally shaped frameworks to explain their illnesses, all possibly valid [30]; (I) the neuropsychological model, considering the loss in self-awareness and self-concern as a sign of frontal lobe damage [31]; and (J) the neurobiological model.
The neurobiological basis of insight was comprehensively explained by Xavier and Vorderstrasse [32] in their 2016 review. They stated that different insight types (clinical, cognitive, metacognitive) are based on different neuroanatomical sites. The first and the most studied is clinical insight, which has been found to originate from multiple brain regions, the most relevant being the prefrontal cortex, cingulate cortex, and regions of the temporal and parietal lobe (precuneus and inferior parietal lobule). Moreover, different insight dimensions have been found to be caused by different alterations in the brain. For example, poor illness awareness was associated with cortical thinness in the dorsolateral prefrontal cortex (PFC) and inferior temporal gyri; poor awareness of treatment necessity was linked to the same structures plus the precuneus [33]. Symptoms misattribution were related to differences in cortical thickness in the orbitofrontal cortex [34]. In addition, hemisphere asymmetry, more specifically a decreased right hemisphere volume in the anterior temporal lobe, dorsolateral PFC, and parietal lobe, has been found in patients with poor clinical insight, particularly illness unawareness [35], results similar with those of neurological patients suffering from anosognosia [36]. Cognitive insight is thought to be based on two neuroanatomical formations: the hippocampus, which together with the fornix is implicated in the “self-certainty” component [37], and the medial PFC, which is essential for the “self-reflectivity” component [38]. The hippocampus (the cognitive system involved in verbal memory) has been found to be specifically involved in cognitive insight, and not in clinical insight [39]. Metacognitive insight is considered to derive from the prefrontal gray and white matter [23], but more research is required to understand this subject.
Recently, besides the traditional explanatory models of insight, a new model linking insight with empathy has been proposed by Thirioux et al. in their study [40]. They stated that insight requires two stages—recognition and acceptance of the disorder. Recognition of the mental illness is gained by taking another person’s perspective and reflecting from that point of view over the own mental state. Furthermore, acceptance of illness involves empathic capacities, meaning that if a patient is able to feel and understand what another person is thinking about him/herself, separated from their own feelings about self; then, they could be able to truly accept their mental state and experiences as pathological.

5. Measurement of Insight with Scales

After dividing insight into smaller dimensions, measurement instruments that can evaluate and quantify every insight dimension were developed. There are many questionnaires that assess clinical insight into psychotic disorders. Starting from David’s three-item classification of insight (awareness of mental illness, recognition of a need for treatment, and ability to re-label symptoms), they comprised multiple insight dimensions expressed in different-length questionnaires (Table 1). For example, the Birchwood Insight Scale (BIS) only covers David’s insight dimensions. Others are more extensive, the largest one being the Scale to Assess Unawareness of Mental Disorders (SUMD), which comprises six general questions and four sub-scales with seventeen items each. Inspired by Amador and David’s presentation of “Aspects of Insight Assessed by Different Instruments” [11], we developed a similar table with all of the clinical insight scales mentioned below (Table 2). This table summarizes what dimensions of clinical insights are represented in each of the five insight scales: the Birchwood Insight Scale, Insight and Treatment Attitude Questionnaire, Schedule for the Assessment of Insight—Expanded, Insight Scale (Markova and Berrios’ second version), and Scale to Assess Unawareness of Mental Disorders. As can be seen, no insight scale depicts all insight dimensions, each of them focusing on specific aspects, and even though most aspects are presented in most scales, there are no two scales with perfect overlap. Moreover, even if all instruments evaluate present insight, only two of them (ITAQ and SUMD) are concerned with past insight and only SUMD focuses also on future insight.
While certain scales have been developed for assessing cognitive insight (Beck Cognitive Insight Scale—BCIS) or evaluating affective disorders (Insight Scale for Affective Disorders—ISAD), insight can also be assessed using general scales, such as the Present State Examination and Positive and Negative Syndrome Scale (PANSS—G12 item).
Given the topic of this paper, the question of which scale is best used for forensic settings arises. In our literature search, we found studies that evaluated forensic outpatients only by the G12 item of the PANSS scale [41] but also studies developed in forensic hospitals that administered more extensive questionnaires, such as the SUMD [42,43], SAI [44], BIS [45], or even BCIS [46]. Thus, the forensic setting does not seem to constitute an impediment in applying longer scales or for assessing cognitive insight. Specifically for the forensic population, the Eisner scale [47] was developed in 1989 to evaluate the discharge readiness of patients. The scale analyzes “forensic insight” or the insight into legal complications of illness through three items (concern about becoming ill, relationship of illness to crime, and acceptance of responsibility for crime). However, we could identify only one study that applied this scale [48].

6. Clinical Implications of Insight

Insight can affect many aspects of a patient’s disease and life. Starting from the synthesis made by Chakraborty and Basu [17] in their study and after an examination of the current literature, we reached a listing of clinical implications of insight, described as follows. (A) Unawareness of the mental illness can increase illness severity, especially when mediated by treatment non-compliance. (B) Poor insight, and especially poor cognitive insight, has been linked to more severe levels of positive, negative, and disorganized symptoms, but results on the relationship between insight and psychopathology are inconsistent [49]. (C) Many studies reported that patients with good insight are more prone to depressed mood, a finding known as the “insight paradox”. In contrast with the beneficial effects of good insight, patients can paradoxically experience another problem, namely hopelessness or demoralization, which leads to depression and even an increased risk of suicide [50,51,52,53,54]. Starring et al. [55] linked this in direct association with perceived stigma, stating that patients with good insight accompanied by stigmatizing beliefs have the highest risk of experiencing low quality of life, negative self-esteem, and depressed mood. (D) Patients who do not believe that they are suffering from a mental illness are usually less likely to accept medical treatment for it; thus, poor insight can lead to treatment noncompliance. At the same time, non-adherence to medication can worsen psychiatric symptoms and consequently the patient’s insight [49,56]. (E) The results regarding insight’s influence on quality of life are inconsistent, with some studies reporting a better functional outcome and quality of life in patients with good insight [51], and other studies showing low quality of life mediated by increased awareness of illness [57] and self-stigma [55]. (F) The severity of the mental illness also affects people surrounding the patient, relatives frequently describing low levels of their own well-being [58]. (G) Patients with poor insight have an increased risk of being involuntarily admitted to a psychiatric emergency unit, as opposed to patients with good insight, who are more likely to present voluntarily to the emergency room and to accept psychiatric hospitalization and care [59]. (H) The relationship between insight and aggressive behavior will be extensively addressed below. (I) Impaired decision making and competence to consent have been found in a sub-group, but not in all patients with poor insight, underlying the importance of assessing this aspect at individual level [60]. (J) Stigma is a fundamental problem that patients with severe mental disorders face, independently of the level of insight. However, increased self-stigma can contribute to the negative effects of good insight, as stated above [55].

7. Overview of Violent Behavior

People suffering from mental illnesses, particularly from psychotic disorders, bear a high level of stigmatization from the cultural association of their disease with violent behavior. In reality, patients suffering from schizophrenia spectrum disorders have a lifetime prevalence of violence of 10% [61], in the context of a schizophrenia prevalence in the general population of roughly 0.7% [62]. Hence, the risk of violence is more an overestimation than a proven fact. However, violent behavior is indeed more present in patients suffering from schizophrenia compared to the general population, with an increased probability (1–7 times) of acting violently throughout their life. For women, the odds even rise to 4–29 times [63].
A study from 2022 by Krakowski et al. [64] claimed that violence in schizophrenia and psychosis holds a different causal pathway from the violence seen in the general population. They divided the antisocial traits associated with the psychopathology of violent behavior into two features: impairment in fear recognition and aggressive reactivity, stating that in non-psychotic violence, the two act in a complementary way, but in schizophrenia patients, they have different etiologies and represent alternative neural pathways to violence.
In another study, Rund et al. [65] suggested that violence in schizophrenia may follow at least two distinct approaches: one associated with premorbid conditions, including antisocial conduct and substance abuse, and one associated with the acute psychopathology of schizophrenia.
These differences are also seen in the victims of the violent attacks. In mentally ill patients, the aggressive behavior is often directed towards caregivers, in contrast to non-mentally ill offenders, whose victims can be strangers [66]. This high prevalence of violent acts can increase burden and stigma and decrease the well-being of family members of patients with mental disorders [67].

7.1. Neurobiology of Violent Behavior

The biological basis of aggressive behavior is complex and comprises anatomical structures, neurotransmitters (serotonin, dopamine, glutamate, gamma aminobutyric acid—GABA), hormones (orexin, oxytocin, vasopressin), genes (monoaminoxidase A—MAOA—also known as the “warrior gene” or “criminal gene”, catechol-O-methyltransferase—COMT, opioid receptor Mu 1—OPRM1), and inflammatory markers (tumor necrosis factor alpha—TNFα and interleukins-1, 4, 6, and 10). All brain regions are implied in this behavior, and the particular structures include the anterior cingulate cortex, prefrontal white matter, prefrontal cortex, and orbitofrontal cortex in the frontal lobe; the precuneus and angular gyrus in the parietal lobe; the superior temporal gyrus, temporoparietal junction, and temporal white matter in the temporal lobe; the cuneus in the occipital lobe; and the striatum, septum, ventral tegmental area, hippocampus, hypothalamus, and amygdala in the limbic system (Table 3) [68,69].
Zooming in on the neurotransmissions implied in aggressive behavior, several serotonin (5-HT), dopamine (D), GABA, and glutamate receptors, as well as the dopamine transporter (DAT), can predispose people to aggressiveness. Data in the literature and evidence regarding serotonin neurotransmission state that the activation of 5-HT2A and 5-HT3 receptors was associated with increased aggressive behavior [84]. Data about the dopamine neurotransmission correlate the aggressive behavior with a DAT blockade and a lower density of type 2-dopamine receptors (D2, D3, and D4) in caudate and putamen [85,86,87]. Inhibition of the GABAA receptor activity, especially in the anterior cingulate cortex, AMPA Glu3 receptor (AMPA—α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid, Glu—glutamate) dysfunction, and inhibition of N-methyl-D-aspartate (NMDA) receptors with low-dose antagonists have all been linked to aggressive behavior [70,88,89,90,91]. Several substances have been known to precipitate or reduce aggressiveness, based on their affinity for these receptors and transporters.

7.2. Drug-Induced Violent Behavior

7.2.1. Anabolic Androgenic Steroids (AASs)

AASs are commonly used to enhance the physical performance of athletes, to rapidly increase muscular mass and strength, and for doping purposes in various sports competitions. The administered equivalent doses for performance-enhancing purposes are 250–5000 mg/week, which are considered supraphysiological doses, exceeding by 5–100 times the natural production of testosterone in men. Chronic use of AASs has been associated with somatic adverse effects such as acne, gynecomastia, and potency problems, and more frequently with psychiatric adverse effects, including aggressiveness, anxiety, and sleeping and mood disorders [92,93].
Aggression and violence account for the highest prevalence of adverse effects in high-dose AAS users. AASs can easily pass through the brain–blood barrier (BBB) and several mechanisms have been proposed, including the interaction with the androgenic receptors in the central nervous system (CNS) and modifications in the serotonergic, dopaminergic, and glutamatergic pathways. It has been suggested that AASs enhance the activation of D2 receptors from supraoptic neurons onto hypothalamus, stimulate 5-HT2A receptors in hypothalamus, and increase the excitatory neurotransmission following the induction of NMDA receptor phosphorylation [93,94].
Forensically, it has been shown that chronic AAS users have a nine times greater risk of being convicted of a crime compared to the general population, according to a study published by Christoffersen et al. in 2019 [95].

7.2.2. Alcohol

Strong evidence correlates abusive alcohol intake with an increase in violence and aggressive behavior, with consequences for both the drinker and their victims due to sustained injuries. The risk is further increased if psychiatric comorbidities or other substances are associated [68,96].
The mechanisms of alcohol-induced violence include the inhibition of PFC and stimulation of dopamine release in striatum, in acute alcohol intake, and serotonin neurotransmission impairment in PFC and amygdala in chronic alcohol intake [97].
Forensically, reports in Europe estimated that out of all public violent incidents, 50% were linked to alcohol in the United Kingdom and between 26% and 43% in Germany, Austria, and the Netherlands. Moreover, out of all alcohol-related incidents, 80% of them were related to nightlife. In the United States, it was more likely for women than men to suffer the consequences of alcohol use by a partner or family member, while more men were reported driving under the influence of alcohol [98,99].

7.2.3. Cannabis

Chronic use of cannabis and withdrawal have been associated with an increased risk of altered mental health and behavioral issues, including aggressiveness and increased impulsivity. Several factors can predispose cannabis users to aggressivity, including environmental and genetic predispositions and differences between sexes and genders. Moreover, the endocannabinoid system takes part in the modulation of aggressiveness through the CB1 receptors, which are abundant in GABAergic and glutamatergic neurons and modulate the release of their neurotransmitters, which have been previously shown to be part of the neurobiology of aggressivity [100,101].
Following the legalization of recreational cannabis use in some countries, there has been an increase in domestic violence cases. For example, in the United States, cities like Denver and Aurora experienced an increase of 48.2% in domestic violence cases. However, this observation is not generally valid. For example, in Canada, following legalization in 2018, the cannabis-related criminalization rate among adults decreased [102,103].

7.2.4. Stimulants

Stimulant drugs include all categories of substances used in pharmacological neuroenhancement, whether they are over-the-counter (OTC) drugs (methylxanthines, pseudoephedrine, herbal medicines, vitamin supplements, and homeopathic preparations), prescription substances (modafinil, methylphenidate, amphetamine, methamphetamine), or illegal substances (amphetamines, cocaine, cathinones, MDMA—3,4-methylenedioxymethamphetamine etc.) [104].
Methamphetamine and amphetamine may increase aggressivity and violent behavior; however, the link between them is unclear. While their mechanism is based on the increased release of dopamine, norepinephrine, and serotonin, all of which modulate the neurobiology of aggression, a systematic review published by O’Malley et al. concluded that acute administration of methamphetamine or amphetamine did not increased the risk of aggressive behavior [105]. However, concomitant use with alcohol has been demonstrated to increase aggressivity, mainly due to alcohol, which is demonstrated to enhance impulsivity and violence [106].

7.2.5. Hallucinogens and Empathogens

Hallucinogens or classical psychedelics act as agonists of the 5-HT2A receptor, inducing an experience characterized by ego dissolution and a sense of invincibility, which can facilitate aggressiveness in users. On the other hand, MDMA, an empathogen, acts directly on the monoamine neurotransmitters and modifies blood flow in brain regions that regulate fear-based behaviors. The latest literature evidence suggests mixed results regarding the link between hallucinogens, MDMA, and aggression [107].

7.2.6. NMDA Receptor Antagonists

Antagonists used for recreational purposes, such as phencyclidine or 3-methoxy-phencyclidine, can cause aggression through their psychosis-inducing effects. Similarly, high doses of dextromethorphan, a weak NMDA receptor antagonist, can induce psychosis and hence increase the risk of aggressivity [108,109].

7.2.7. Heroin

Heroin and other opioids can facilitate aggressive behavior through the behavioral changes that they can induce during use and the withdrawal syndrome. During drug use, increased levels of dopamine are released, resulting in intensive craving and addictive behavior [110].
According to a study conducted by Maremmani et al., eight out of every ten patients with heroin use disorder displayed aggressive behavior, 23.8% of which showed verbal hostility, irritability, negativism, and indirect hostility, while the other 76.2% showed suspicion, resentment, assault, and guilt [111].

7.2.8. Anticonvulsants

Levetiracetam, perampanel, topiramate, brivaracetam, tiagabine, vigabatrin, and zonisamide have been associated with an increased risk of aggressive behavior compared to other anticonvulsant drugs. A proper pharmacological mechanism of action could not be ruled out, but based on several observations, the induced aggressiveness may be caused by the inhibition of the AMPA receptor and alterations in serotonin and GABA levels. A relief in the aggressive behavior has been observed when switching from levetiracetam to brivaracetam, representing a potential option in clinical practice [112,113,114].
The relation to insight, possible mechanisms related to aggression and violence, and psychiatric symptoms of the aforementioned drugs are summarized in Table 4.

8. Measurement of Violence with Scales

There are several violence risk questionnaires, each targeting particular features or subject groups. A list of such questionnaires along with their corresponding extent and form of rating is presented in Table 5.
Numerous scales evaluate patients solely through observation during interviews, considering various aspects, illustrated in Table 6. These scales are usually used to assess the violence risk of patients admitted into a psychiatric unit. At the end, it results in a final score which corresponds to the violence risk or, in the case of the NOIIS scale, a graph similar to a temperature scale [125].
Other scales are based on both psychiatric interviews and information from patients’ clinical files, including demographic information regarding childhood and educational trajectory. The HCR-20 is one of the most used scales in studies evaluating violence among psychiatric patients. It consists of ten historical, five clinical, and five risk-management items and can be applied in both clinical and forensic settings [126]. The START tool is a more exhaustive instrument that explores a patient’s strength and vulnerabilities related to 20 factors, developing 7 risk estimates (violence, self-harm, suicide, unauthorized leave, substance abuse, self-neglect, and being victimized) [127]. The VRAG-R, PCR, VRS-2, and SAQ are more often used in forensic settings. The VRAG-R uses clinical records to assess the patients’ risk of violence recidivism and is suitable for male patients who have committed serious violent or sexual offenses [128]. The PCR uses interviews and information from the patient’s file record to appraise the patient’s level of psychopathy [129]. It is composed of questions addressing emotional detachment and antisocial behavior. The VRS-2 consists of 6 static factors regarding the patient’s upbringing and past offenses and 20 dynamic factors, assessed through interview, noting the stage of change in each domain. It can be used to monitor variations in risk and motivation to change, especially for forensic psychiatric patients which are considered for community access [130]. The SAQ is the most different from the others by virtue of being (as the name implies) a self-administered test. The items are classified into eight subscales: criminal tendencies, antisocial personality problems, antisocial personality disorder, conduct problems, criminal history, alcohol/drug abuse and antisocial associations, anger, and a final validity item, the last two not taking part in the total score. It is used for both assessing violence risk and recidivism and assignment to a suitable treatment program [131].
Finally, a unique violence risk assessment tool is the Classification of Violence Risk (COVR), which is an interactive software program designed to estimate the risk of a person hospitalized for a mental disorder to be violent to others. After a chart review and a brief interview with the patient, the software generates an estimation of the violence risk, ranging from 1% to 76% [132].

9. The Relationship Between Insight and Violent Behavior: The Influence of Confounders

There is no settled answer for the question “Is insight an actual risk factor for violent behavior in psychosis?” In their review from 2019, Smith et al. [133] reported that among 18 studies published between 1980 and 2019, only 8 demonstrated a positive relationship between poor insight and violence. They also described the limitations of each study, proving that consistent, reliable results are difficult to obtain. Among these limitations, we mention small sample sizes, the retrospective design of the study, inappropriate scales for assessing insight dimensions, heterogenous definitions for violent behavior, not differentiating between past and present insight, and not excluding the impact of confounding factors, like positive symptoms, psychopathy, and substance abuse.
A study from 2018 by Schandrin et al. [134] with 666 patients with schizophrenia from 10 tertiary centers and using three insight instruments (SUMD, BIS, and PANSS G12 item) stated that specific insight dimensions were linked to specific sub-types of aggressive behavior. They described aggressivity as a multi-dimensional approach, considering an emotional component (anger) and a cognitive component (hostility). They found that hostility increased with insight, but this relationship faded when controlling for the potential confounding effect of depression (often associated with increased insight). A possible underlying mechanism could be that high insight increases self-stigma, which increases depression and could also lead to the expression of an underlying hostile tendency (trait). Furthermore, insight into the consequences of illness, especially partial or unstable insight, was associated with the more impulsive and reactional dimensions of aggressiveness, namely anger and physical aggressiveness.
A recent study from 2023 by Fischer-Vieler et al. [135] compared patients with a diagnosis of a psychotic disorder with patients without known psychiatric conditions, assessing insight with the BIS and PANSS G12 tools, and stated that a history of violence was significantly associated with lower insight, even after controlling the confounders. However, they did not take into account the possible confounder effect of psychopathy. In addition, the assessed violent events had taken place, in some cases, long before the moment of insight assessment. A study from the same year analyzed the influence of cognitive insight and functional remission on criminal behavior in schizophrenia and concluded that with an increase in symptoms’ severity came a decrease in a patient’s insight and functional remission, with a tendency towards criminal behavior [136].
A narrative review from 2015 by Lamsma and Harte [137] on 69 studies between 1990 and 2013 noted that the relationship between psychosis and violence is more intricate than initially thought and proposed a diagram of 41 possible interrelated pathways, binding insight to violence both directly and indirectly, mediated by treatment non-adherence.
Regarding bipolar disorder in particular, the available literature is scarce. In a study from 2010 by González-Ortega et al. [138], the authors concluded that aggressive behavior during acute manic episodes was linked to positive symptoms, involuntary admissions, and lack of insight, but they quantified insight only through the G12 item of PANSS. A more recent study from 2019 by Luo et al. [139] found that poor insight, measured by the ITAQ, was associated with increased rates of involuntary admission. A study from 2017 by Pompili et al. [140] noted that aggressive behavior occurred mainly in manic episodes but when comparing euthymic patients with healthy controls, the violence rates were higher in the euthymic group. A study conducted by Asgarabad et al. in 2022 found out that the awareness of the disorder in schizophrenia was more impaired compared to bipolar affective disorder, but that similar levels were observed for the awareness of medication effects, social consequences, and clinical insight [141]. There is scarce information regarding the differences in traits of aggression and violence between bipolar affective disorder and schizophrenia, with some authors claiming an increased risk of violence in bipolar disorder, especially during manic episodes [142].
As expected, insight is one of the many factors having an impact on a patient’s tendency towards violent behavior. Numerous studies from the last two decades have focused on the risk factors for violence, dividing them into static and dynamic. Static risk factors, present in the HCR-20 v3 as historical risk factors, include criminal histories [143] such as previous violence [144,145,146]; childhood misconduct [147,148]; prior convictions; substance [65,143,145,147,148,149,150] and alcohol abuse [143,146]; comorbid psychiatric diagnoses, especially psychopathy [65,144] and other personality disorders [151]; and poverty and social disadvantages [147,152,153]. In contrast, dynamic risk factors, found in the HCR-20v3 under clinical risk factors, comprise the following: positive symptoms, non-adherence to treatment [143,154,155], poor insight [48,65,133,144], and impulsivity [65,126]. Negative symptoms, such as social withdrawal and blunt affect, have been found to hold a protective role for violence [147,148].
In their review, Steinert et al. [156] stated that clinical and psychopathological variables are more predictive for inpatient violence, while static risk factors are more applicable to community violence.
Nevertheless, not all of the factors mentioned above contribute equally to the risk of violent behavior. The level of impact of each factor related to violent behavior is, to some degree, particular to each paper that studied it. In their review of 110 studies, Witt et al. [143] divided the factors into strong, moderate, or weak associations with violent behavior in psychosis. A strong association was found in the case of a history of violent acts, non-adherence with psychological treatments, substance use disorder, positive symptoms, lack of insight, and poor impulse control. Non-adherence to medication and comorbid antisocial personality disorder were found to be moderately associated with violence. A more detailed illustration of the findings from the review is represented in Figure 1. Somewhat controversial results were presented by a review from 2018, which found that lack of insight had a more severe effect on violence than positive symptoms, naming insight “the only single variant that could predict violent behavior” [65]. Although intriguing, the results of the studies included were mixed and the other important confounders must be taken into consideration.
The relationship between insight and violence is at least partly mediated by two important factors: positive symptoms and treatment non-adherence. With regard to positive symptoms, an important mention would be that, although patients with poor insight often exhibit severe positive symptoms, as demonstrated by other studies [157,158], better insight scores were seen in patients only with hallucinations compared to patients only with delusions. As Galletti et al. explained, hallucinations represent a greater breaking experience from the outside world, which is easier for the patient to recognize as not real [159]. As discussed by Lincoln et al. in their review, the relationship between insight and symptoms’ severity over time is complex and worth more research [133]. Furthermore, low insight was associated in many studies with poor compliance with pharmacological and psychosocial therapies [42,133,160,161,162].
A very important risk factor for violence, often seen as a comorbidity in patients with psychotic disorders, is represented by alcohol and substance abuse. A study from 2008 by Rueve and Welton [66] that discussed the problem of violence in mental illness mentioned that patients with alcohol and drug use had more arrests over their lifetime than patients with schizophrenia, personality disorders, or affective disorders. They also noted that patients suffering from both substance use disorders and personality disorders were 240% more likely to commit violent acts than mentally ill patients without substance abuse comorbidity, although the sources cited were too outdated to be taken without a doubt. Lamsma et al. [137] named substance abuse a major predictor for violence in psychosis and suggested four possible mechanisms by which substance use could increase the risk for violence: (a) through their neurobiological effects, by reducing inhibitions; (b) by having a detrimental effect on a patient’s social support system; (c) via the buying and selling of illegal drugs, which often take place in criminogenic environments; (d) by aggravating psychotic symptoms. The study from 2018 by Rund et al. [65] named comorbid substance abuse in schizophrenia “the most severe form of violence”, although not all studies agree on this. Other papers found that recent alcohol and drug misuse were significant risk factors for both severe and less severe violence [143]. In general, studies agree that substance use disorders lead to a significant increase in the risk of violence, but that is not a homogeneous finding and there is an urgent need for fresh data on this subject.
When addressing the influence of a patient’s history on the risk of violence, Witt et al. [143] found that criminal history factors, such as previous violent acts and prior arrests, were more strongly associated with violence than substance misuse and demographic factors, but other studies presented conflicting results.
Finally, stressful situations and events can also increase the risk of violence, as described by many studies in the context of the COVID-19 pandemic, when social isolation, economic strain, childcare stress, and virus-related fears led to a higher number of violent acts. As mentioned by Whiteman et al., the most affected population consisted of people who already did not live in a safe environment previous to the pandemic, the most frequent victims being women, children, and elderly people [163,164].

10. Does Diagnosis Matter?

There remains the question of how this relationship is influenced by the diagnosis. We know that bipolar disorder bears a better prognosis than schizophrenia, but do patients with schizophrenia present more severe violent behavior compared to patients with comparable levels of insight but with a diagnosis of bipolar disorder? And can we compare insight into two separate illnesses?
Research that could give an answer to these questions was difficult to find. When addressing the comparison between diagnoses, studies usually focus only on insight or only on violent behavior. Regarding insight, the results were mixed. Some studies described poorer insight in schizophrenia [165], but this could become non-significant when adjusting for age [166]. Others observed lower insight in schizophrenia but only in specific dimensions, such as the need for treatment and presence/outcome of illness, as described in a study from 2019 by Huang and Chang [167], or symptom re-labeling, as illustrated by a paper from 2007 by Varga et al. [168], which also suggested that differences in general insight (in illness awareness) could be better explained by symptom severity and deficits in working memory function than by the specific diagnosis.
With respect to violent behavior, research was even more lackluster. A paper from 2014 by Robertson et al. showed that patients with bipolar disorder, especially with comorbid substance abuse, had an increased risk of violent behavior than patients with schizophrenia, especially when not associated with substance abuse [169]. Although intriguing, substance abuse is known to be an important independent risk factor for violent outbursts and more research on this subject is required before reaching a firm conclusion.

11. Limitations of Studies Assessing Insight/Violence

There are not many available studies assessing the relationship between insight and violence, especially in recent years. After analyzing the existing literature, which comprised heterogenous study protocols and, consequently, contrasting results, we wanted to point out a few important aspects to bear in mind when designing a study on this subject. Inspired by the review by Smith et al. [133] and several other reviews and meta-analyses [63,65,137,143], we gathered a list of identified limitations. These can be classified into the following: (1) factors regarding study design, namely small sample size and retrospective design; (2) factors regarding insight—inappropriate scales for assessing the insight dimensions and the lack of differentiation between past, present, and future insight, leading to false conclusions when comparing a past offense with a patient’s present insight; (3) factors regarding violent behavior—heterogenous definitions for violence, distinct reports of violent behavior (by the patient, by family, by law enforcement, or by medical staff); (4) factors regarding the psychiatric diagnosis—different results in different psychotic conditions and insufficient data concerning bipolar disorder; (5) the importance of excluding confounders; (6) patients’ drop-out.

12. Treatment Options in Forensic Psychiatric Settings

According to a systematic review conducted by Howner et al., knowledge regarding pharmacological treatment in forensic psychiatry settings is limited. Therefore, targeting the receptors that mediate aggressive behavior and violence represents the most rational treatment choice in patients displaying these characteristics. Parenterally administered antipsychotics represent the most frequently used drugs for the chemical restraint of aggressive patients, with haloperidol being the most used agent out of all antipsychotics. Their efficacy in the management of these situations is due to their antagonist activity on the 5-HT2A (atypical antipsychotics) and the D2 (typical antipsychotics) receptors. Other commonly used chemical restraint options reported in the literature were parenterally administered benzodiazepines and intravenous (i.v.) sodium valproate. Several studies on animal models have demonstrated that setrons, which are antagonists of the 5-HT3 receptor, can also reduce aggressivity [84,170,171].
Since the MAOA gene is referred to as the “warrior gene” or “criminal gene”, the potential of monoamine oxidase inhibitors (MAOIs) to reduce aggressive behavior have been taken into consideration. However, animal studies have shown that MAOIs have different influences depending on the developmental stage, selectivity on A or B types, and dosages [69].
As previously stated, high doses of NMDA antagonists can reduce aggressive behavior. Examples from the literature include a 4–5 mg/kg intramuscular ketamine single dose or 20 mg/day of memantine [172].
Besides pharmacological treatment, there have been described several non-pharmacological interventions in forensic psychiatry settings, including neurocognitive training, cognitive–behavioral treatment programs like Reasoning and Rehabilitation (R&R), Effect of Life Minus Violence—Enhanced, Positive Behavioral Support (PBS), the therapeutic theater project, and mindful yoga [173].
Before applying chemical restraining methods, it is advisable to use de-escalation techniques meant to recognize early signs of anger in patients and to bring them into a calmer state. These techniques are composed of both verbal communication (e.g., negotiation, tactful language, calm tone, etc.) and non-verbal communication skills, like posture, body language, active listening, or an empathetic attitude [174,175,176].

13. How to Increase Medication Adherence?

As previously stated, reduced medication adherence represents one of the main causes for lack of insight and an increasing risk of violence [56]. According to Velligan et al., non-adherence contributed to the lack of insight in 55.6% of the studies (20 out of 36) taken into consideration, exceeding other causes such as substance abuse, medication-related side effects, and cognitive impairment [177]. Other statistics suggest that medication non-adherence is as high as 63–74% in patients with schizophrenia and 50% in patients with bipolar affective disorder [178].
The main cause of non-adherence was a negative attitude towards medication, which can be fueled by factors like hostility and uncooperativeness at first admission, lack of information regarding the treatment, the cost of and access to treatment, stigma, effectiveness, possible side effects, complexity of regimens and possible risk of drug–drug interactions, doses, formulation, and the belief of some patients that treatment is no longer necessary when they sense a good response to treatment in the early phases [177,179,180].
Several interventions can be used in order to increase treatment compliance. These strategies can be either addressed to the patient or to the medication they are taking. Patient-directed interventions include psychoeducational programs (group therapy and meetings, in which the family can be encouraged to participate), individualized interventions, motivational approaches, behavioral strategies, family support, and the establishment of a strong therapeutic alliance. Treatment-directed interventions aim to improve efficacy, safety, and adherence. The improvement of efficacy includes dose adjustments and the selection of the best choice of treatment, given the clinical evidence and past experiences, while safety is achieved by proper management of the adverse effects and drug–drug interactions [180].
Adherence can be tracked through traditional pill counting or using electronic medication monitoring systems that can record each time the bottle is opened. However, none of these methods can rule out if the pills are taken out and discarded without ingestion. Therefore, novel technologies such as ingestible sensor use can be employed. An example of such approved technology is Abilify® MyCite (aripiprazole), which tracks if the pill has been ingested through a wearable patch and a smartphone application. Data in the literature evidenced an increased adherence of between 73.9% and 88.6% in patients with schizophrenia, bipolar affective disorder, and major depressive disorder. Disadvantages of using ingestible sensors include a decreasing need for communication between the patient and the healthcare professional, which can weaken the therapeutic alliance, increased costs, potential inadequate usage for patients with surveillance paranoia, and even ethical concerns, such as restriction of the patient’s autonomy [180,181,182,183,184].
The acceptance of long-acting injectable (LAI) antipsychotics can be improved using shared decision making, by presenting the necessary information to the patient in a simple and clear manner, and by listening to their preferences, fears, and/or past negative experiences regarding LAI antipsychotics. The healthcare professional must reassure the patient regarding the benefits of LAI, namely the better efficacy compared to oral treatment in the prevention of relapses and the better overall outcome if initiated during the early phases of the illness. There is an increased chance of improving treatment adherence if the patient’s involvement in the choice of therapy is accompanied by constant communication and the work of comparison with the medical staff [185].

14. Conclusions

In this review, we wanted to present the complex relationship between insight into psychiatric illness and violent behavior. For this purpose, we described the concept of insight and its origins, dimensions, explanatory models, measuring scales, and implications. One of the implications of impaired insight was seen to be an increased risk of violent behavior. However, there are many factors that can lead to increased aggressivity, starting from a genetic predisposition and the psychotropic effects of medication and other substances, but also including demographic and clinical factors specific to each patient. Both insight and violent behavior can be assessed through several questionnaires, each of them with their features and indications.
There is a continuous debate in the literature regarding what clinical factors influence the most violent behavior. Positive symptoms, non-adherence to medication treatments, substance and alcohol abuse, and a history of aggressive behavior and personality disorders are only a few that enhance the chance of a patient without insight into their illness acting in a violent manner. On the other hand, negative symptoms and depression have been found to provide a protective role against violent behavior. Therefore, in clinical practice, it is important to be aware of and reduce the impact of any factor that may contribute to the lack of insight of a patient and predispose them to violence.
Several interventions like motivational interviews, medication reconciliation, or various psychoeducational programs should be applied for a better therapeutic alliance, while chemical restraint should be reserved only for emergencies, when no de-escalation is possible.
For reliable research on the relationship between insight and violent behavior, the definitions and extensive classifications of insight and violence must be understood, while proper measuring scales for the specific investigated dimensions must be used.
Finally, because of the many controversial results on this topic, more comprehensive and updated research is required.

Author Contributions

Conceptualization, B.-M.H. and C.-A.C.; methodology, B.-M.H.; writing—original draft preparation, B.-M.H., D.U. and C.-A.C.; writing—review and editing, B.-M.H., D.U. and C.-A.C.; visualization, B.-M.H.; supervision, C.-A.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in this article.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Crișan, C.A. Lack of Insight in Bipolar Disorder: The Impact on Treatment Adherence, Adverse Clinical Outcomes and Quality of Life. In Psychotic Disorders—An Update; InTech: London, UK, 2018. [Google Scholar]
  2. Crișan, C.; Pop, R. Predictors of Schizophrenia Clinical Evolution. Psihiatru.ro 2023, 73, 22–26. [Google Scholar] [CrossRef]
  3. Crișan, C.; Vlasin, N.; Dutchievici, I.; Nemeș, A.; Micluția, I. Awarness of Illness, Depression and Self-Stigma in Romanian Patients with Schizophrenia. Cogn. Brain Behav. 2016, 20, 345–355. [Google Scholar]
  4. Crisan, C.A.; Pintea, S.; Miclutia, I.V.; Macrea, R. The Relationship between Insight and Psychopathology in First-Episode Schizophrenia. Rom. J. Psychopharmacol. 2011, 11, 189–199. [Google Scholar]
  5. Crisan, C.A.; Pintea, S.; Miclutia, I.; Macrea, R. The Predictive Role of Insight for the Evolution of the Disease in Romanian Patients Diagnosed with Schizophrenia. Eur. Psychiatry 2017, 41, s809. [Google Scholar] [CrossRef]
  6. Fazel, S.; Wolf, A.; Fimińska, Z.; Larsson, H. Mortality, Rehospitalisation and Violent Crime in Forensic Psychiatric Patients Discharged from Hospital: Rates and Risk Factors. PLoS ONE 2016, 11, e0155906. [Google Scholar] [CrossRef]
  7. Broderick, C.; Azizian, A.; Kornbluh, R.; Warburton, K. Prevalence of Physical Violence in a Forensic Psychiatric Hospital System during 2011–2013: Patient Assaults, Staff Assaults, and Repeatedly Violent Patients. CNS Spectr. 2015, 20, 319–330. [Google Scholar] [CrossRef]
  8. Crisan, C.A.; Bondor, C.; Macrea, R. Lack of Insight in Schizophrenia: Prognostic Factor for the Evolution of the Disease. Acta Medica Marisiensis 2010, 56, 517–521. [Google Scholar]
  9. Dumbrava, D.; Ureche, D.; Rebeleanu, C.; Siserman, C.; Crișan, C.; Miclutia, I. Legal Guardianship of the Psychiatric Pateint—Psychiatric and Forensic Perspectives. Rom. J. Leg. Med. 2020, 28, 21–27. [Google Scholar] [CrossRef]
  10. Bonea, M.; Crişan, C.; Ureche, D.; Iliescu, D.; Dumbravă, L. Late-Onset Schizophrenia: Diagnosis Difficulties and Legal Implications. Rom. J. Leg. Med. 2019, 27, 69–72. [Google Scholar] [CrossRef]
  11. David, A.S.; Amador, X.F. Insight and Psychosis, 2nd ed.; Amador, X.F., David, A.S., Eds.; Oxford University Press: Oxford, UK, 2004; ISBN 9780198525684. [Google Scholar]
  12. Arango, C.; Barba, A.C.; Gonzalez-Salvador, T.; Ordonez, A.C. Violence in Inpatients with Schizophrenia: A Prospective Study. Schizophr. Bull. 1999, 25, 493–503. [Google Scholar] [CrossRef]
  13. Friedman, L.; Hrouda, D.; Noffsinger, S.; Resnick, P.; Buckley, P.F. Psychometric Relationships of Insight in Patients with Schizophrenia Who Commits Violent Acts. Schizophr. Res. 2003, 60, 81. [Google Scholar] [CrossRef]
  14. Trauer, T.; Sacks, T. The Relationship between Insight and Medication Adherence in Severely Mentally Ill Clients Treated in the Community. Acta Psychiatr. Scand. 2000, 102, 211–216. [Google Scholar] [CrossRef] [PubMed]
  15. Kamali, M.; Kelly, L.; Gervin, M.; Browne, S.; Larkin, C.; O’Callaghan, E. Psychopharmacology: Insight and Comorbid SubstanceMisuse and Medication ComplianceAmong Patients with Schizophrenia. Psychiatr. Serv. 2001, 52, 161–166. [Google Scholar] [CrossRef] [PubMed]
  16. Jaspers, K. General Psychopathology; John Hopkins University Press: Baltimore, MD, USA, 1997. [Google Scholar]
  17. Chakraborty, K.; Basu, D. Insight in Schizophrenia-A Comprehensive Update. Ger. J. Psychiatry 2010, 13, 17–30. [Google Scholar]
  18. Geddes, R.J.; Andreasen, N.C.; Goodwin, G.M. (Eds.) New Oxford Textbook of Psychiatry; Oxford University Press: Oxford, UK, 2020; ISBN 9780198713005. [Google Scholar]
  19. Jacob, K.S. Insight in Psychosis: An Indicator of Severity of Psychosis, an Explanatory Model of Illness, and a Coping Strategy. Indian J. Psychol. Med. 2016, 38, 194–201. [Google Scholar] [CrossRef]
  20. Marková, I. Insight in Psychiatry; Cambridge University Press: Cambridge, UK, 2005; ISBN 9780521825184. [Google Scholar]
  21. Van Camp, L.S.C.; Sabbe, B.G.C.; Oldenburg, J.F.E. Cognitive Insight: A Systematic Review. Clin. Psychol. Rev. 2017, 55, 12–24. [Google Scholar] [CrossRef]
  22. Beck, A. A New Instrument for Measuring Insight: The Beck Cognitive Insight Scale. Schizophr. Res. 2004, 68, 319–329. [Google Scholar] [CrossRef]
  23. Spalletta, G.; Piras, F.; Piras, F.; Caltagirone, C.; Orfei, M.D. The Structural Neuroanatomy of Metacognitive Insight in Schizophrenia and Its Psychopathological and Neuropsychological Correlates. Hum. Brain Mapp. 2014, 35, 4729–4740. [Google Scholar] [CrossRef]
  24. Lysaker, P.H.; Weiden, P.J.; Sun, X.; O’Sullivan, A.K.; McEvoy, J.P. Impaired Insight in Schizophrenia: Impact on Patient-Reported and Physician-Reported Outcome Measures in a Randomized Controlled Trial. BMC Psychiatry 2022, 22, 574. [Google Scholar] [CrossRef]
  25. Grover, S.; Avasthi, A.; Chakravarty, R.; Dan, A.; Chakraborty, K.; Neogi, R.; Desousa, A.; Nayak, O.P.; Praharaj, S.K.; Menon, V.; et al. Insight in Patients with Bipolar Disorder: Findings from the Bipolar Disorder Course and Outcome Study from India (BiD-CoIN Study). Indian J. Psychiatry 2023, 65, 767–773. [Google Scholar] [CrossRef]
  26. Van Putten, T. Drug Refusal in Schizophrenia and the Wish to Be Crazy. Arch. Gen. Psychiatry 1976, 33, 1443. [Google Scholar] [CrossRef] [PubMed]
  27. Mintz, A.R.; Dobson, K.S.; Romney, D.M. Insight in Schizophrenia: A Meta-Analysis. Schizophr. Res. 2003, 61, 75–88. [Google Scholar] [CrossRef] [PubMed]
  28. Saravanan, B.; Jacob, K.S.; Johnson, S.; Prince, M.; Bhugra, D.; David, A.S. Assessing Insight in Schizophrenia: East Meets West. Br. J. Psychiatry 2007, 190, 243–247. [Google Scholar] [CrossRef] [PubMed]
  29. Gambini, O.; Barbieri, V.; Scarone, S. Theory of Mind in Schizophrenia: First Person vs Third Person Perspective. Conscious. Cogn. 2004, 13, 39–46. [Google Scholar] [CrossRef] [PubMed]
  30. Porter, R. Arthur Kleinman, Patients and Healers in the Context of Culture. An Exploration of the Borderland between Anthropology, Medicine, and Psychiatry, Berkeley, Los Angeles, and London, University of California Press, 1980, 8vo, Pp. Xvi, 427, Illus., £15.00. Med. Hist. 1981, 25, 435–436. [Google Scholar] [CrossRef]
  31. David, A.S.; Fleminger, S.; Kopelman, M.D.; Lovestone, S.; Mellers, J.D.C. Organic Psychiatry: A Textbook of Neuropsychiatry; Oxford University Press: Oxford, UK, 1987. [Google Scholar]
  32. Xavier, R.M.; Vorderstrasse, A. Neurobiological Basis of Insight in Schizophrenia. Nurs. Res. 2016, 65, 224–237. [Google Scholar] [CrossRef]
  33. Buchy, L.; Ad-Dab’bagh, Y.; Malla, A.; Lepage, C.; Bodnar, M.; Joober, R.; Sergerie, K.; Evans, A.; Lepage, M. Cortical Thickness Is Associated with Poor Insight in First-Episode Psychosis. J. Psychiatr. Res. 2011, 45, 781–787. [Google Scholar] [CrossRef]
  34. Buchy, L.; Ad-Dab’bagh, Y.; Lepage, C.; Malla, A.; Joober, R.; Evans, A.; Lepage, M. Symptom Attribution in First Episode Psychosis: A Cortical Thickness Study. Psychiatry Res. Neuroimaging 2012, 203, 6–13. [Google Scholar] [CrossRef]
  35. Gerretsen, P.; Chakravarty, M.M.; Mamo, D.; Menon, M.; Pollock, B.G.; Rajji, T.K.; Graff-Guerrero, A. Frontotemporoparietal Asymmetry and Lack of Illness Awareness in Schizophrenia. Hum. Brain Mapp. 2013, 34, 1035–1043. [Google Scholar] [CrossRef]
  36. Ramachandran, V.S. Anosognosia in Parietal Lobe Syndrome. Conscious. Cogn. 1995, 4, 22–51. [Google Scholar] [CrossRef]
  37. Buchy, L.; Luck, D.; Czechowska, Y.; Malla, A.; Joober, R.; Lepage, M. Diffusion Tensor Imaging Tractography of the Fornix and Belief Confidence in First-Episode Psychosis. Schizophr. Res. 2012, 137, 80–84. [Google Scholar] [CrossRef] [PubMed]
  38. Pu, S.; Nakagome, K.; Yamada, T.; Itakura, M.; Satake, T.; Ishida, H.; Nagata, I.; Kaneko, K. Association between Cognitive Insight and Prefrontal Function during a Cognitive Task in Schizophrenia: A Multichannel near-Infrared Spectroscopy Study. Schizophr. Res. 2013, 150, 81–87. [Google Scholar] [CrossRef] [PubMed]
  39. Buchy, L.; Czechowska, Y.; Chochol, C.; Malla, A.; Joober, R.; Pruessner, J.; Lepage, M. Toward a Model of Cognitive Insight in First-Episode Psychosis: Verbal Memory and Hippocampal Structure. Schizophr. Bull. 2010, 36, 1040–1049. [Google Scholar] [CrossRef] [PubMed]
  40. Thirioux, B.; Harika-Germaneau, G.; Langbour, N.; Jaafari, N. The Relation Between Empathy and Insight in Psychiatric Disorders: Phenomenological, Etiological, and Neuro-Functional Mechanisms. Front. Psychiatry 2020, 10, 966. [Google Scholar] [CrossRef] [PubMed]
  41. Lincoln, T.M.; Hodgins, S. Is Lack of Insight Associated with Physically Aggressive Behavior Among People with Schizophrenia Living in the Community? J. Nerv. Ment. Dis. 2008, 196, 62–66. [Google Scholar] [CrossRef]
  42. Alia-Klein, N.; O’Rourke, T.M.; Goldstein, R.Z.; Malaspina, D. Insight into Illness and Adherence to Psychotropic Medications Are Separately Associated with Violence Severity in a Forensic Sample. Aggress. Behav. 2007, 33, 86–96. [Google Scholar] [CrossRef]
  43. Goodman, C.; Knoll, G.; Isakov, V.; Silver, H. Insight into Illness in Schizophrenia. Compr. Psychiatry 2005, 46, 284–290. [Google Scholar] [CrossRef]
  44. Carroll, A.; Pantelis, C.; Harvey, C. Insight and Hopelessness in Forensic Patients with Schizophrenia. Aust. N. Z. J. Psychiatry 2004, 38, 169–173. [Google Scholar] [CrossRef]
  45. McIntosh, L.G.; Slesser, M.; O’Rourke, S.; Thomson, L.D.G. On the Road to Recovery Psychological Therapy versus Treatment as Usual for Forensic Mental Health Patients: Study Protocol for a Randomized Controlled Feasibility Trial. Pilot Feasibility Stud. 2018, 4, 124. [Google Scholar] [CrossRef]
  46. Kudumija Slijepčević, M.; Jukić, V.; Novalić, D.; Žarković-Palijan, T.; Milošević, M.; Rosenzweig, I. Alcohol Abuse as the Strongest Risk Factor for Violent Offending in Patients with Paranoid Schizophrenia. Croat. Med. J. 2014, 55, 156–162. [Google Scholar] [CrossRef]
  47. Eisner, H.R. Returning the Not Guilty by Reason of Insanity to the Community: A New Scale to Determine Readiness. Bull. Am. Acad. Psychiatry Law 1989, 17, 401–413. [Google Scholar] [PubMed]
  48. Buckley, P.F.; Hrouda, D.R.; Friedman, L.; Noffsinger, S.G.; Resnick, P.J.; Camlin-Shingler, K. Insight and Its Relationship to Violent Behavior in Patients with Schizophrenia. Am. J. Psychiatry 2004, 161, 1712–1714. [Google Scholar] [CrossRef]
  49. Lysaker, P.H.; Vohs, J.; Hillis, J.D.; Kukla, M.; Popolo, R.; Salvatore, G.; Dimaggio, G. Poor Insight into Schizophrenia: Contributing Factors, Consequences and Emerging Treatment Approaches. Expert Rev. Neurother. 2013, 13, 785–793. [Google Scholar] [CrossRef] [PubMed]
  50. Belvederi Murri, M.; Amore, M. The Multiple Dimensions of Insight in Schizophrenia-Spectrum Disorders. Schizophr. Bull. 2019, 45, 277–283. [Google Scholar] [CrossRef] [PubMed]
  51. Ouzir, M.; Azorin, J.M.; Adida, M.; Boussaoud, D.; Battas, O. Insight in Schizophrenia: From Conceptualization to Neuroscience. Psychiatry Clin. Neurosci. 2012, 66, 167–179. [Google Scholar] [CrossRef] [PubMed]
  52. Belvederi Murri, M.; Respino, M.; Innamorati, M.; Cervetti, A.; Calcagno, P.; Pompili, M.; Lamis, D.A.; Ghio, L.; Amore, M. Is Good Insight Associated with Depression among Patients with Schizophrenia? Systematic Review and Meta-Analysis. Schizophr. Res. 2015, 162, 234–247. [Google Scholar] [CrossRef]
  53. Cavelti, M.; Rüsch, N.; Vauth, R. Is Living with Psychosis Demoralizing? J. Nerv. Ment. Dis. 2014, 202, 521–529. [Google Scholar] [CrossRef]
  54. Davis, B.J.; Lysaker, P.H.; Salyers, M.P.; Minor, K.S. The Insight Paradox in Schizophrenia: A Meta-Analysis of the Relationship between Clinical Insight and Quality of Life. Schizophr. Res. 2020, 223, 9–17. [Google Scholar] [CrossRef]
  55. Staring, A.B.P.; Van der Gaag, M.; Van den Berge, M.; Duivenvoorden, H.J.; Mulder, C.L. Stigma Moderates the Associations of Insight with Depressed Mood, Low Self-Esteem, and Low Quality of Life in Patients with Schizophrenia Spectrum Disorders. Schizophr. Res. 2009, 115, 363–369. [Google Scholar] [CrossRef]
  56. Kim, J.; Ozzoude, M.; Nakajima, S.; Shah, P.; Caravaggio, F.; Iwata, Y.; De Luca, V.; Graff-Guerrero, A.; Gerretsen, P. Insight and Medication Adherence in Schizophrenia: An Analysis of the CATIE Trial. Neuropharmacology 2020, 168, 107634. [Google Scholar] [CrossRef]
  57. Karow, A.; Pajonk, F.-G.; Reimer, J.; Hirdes, F.; Osterwald, C.; Naber, D.; Moritz, S. The Dilemma of Insight into Illness in Schizophrenia: Self- and Expert-Rated Insight and Quality of Life. Eur. Arch. Psychiatry Clin. Neurosci. 2008, 258, 152–159. [Google Scholar] [CrossRef] [PubMed]
  58. Froböse, T.; Pitschel-Walz, G.; Bäuml, J. Mangelnde Krankheitseinsicht Bei Patienten Mit Einer Schizophrenen Psychose Aus Der Perspektive Der Angehörigen. Psychiatr. Prax. 2009, 36, 373–378. [Google Scholar] [CrossRef] [PubMed]
  59. Smyth, S.; McFarland, J.; McGuiness, D.; Summerville, S.; Bainbridge, E.; Hallahan, B.; Higgins, A.; Casey, D.; Murphy, K.; McDonald, C. A Mixed Methods Study Examining Perceptions by Service-Users of Their Involuntary Admission in Relation to Levels of Insight. Int. J. Soc. Psychiatry 2022, 68, 1764–1773. [Google Scholar] [CrossRef] [PubMed]
  60. Capdevielle, D.; Raffard, S.; Bayard, S.; Garcia, F.; Baciu, O.; Bouzigues, I.; Boulenger, J.-P. Competence to Consent and Insight in Schizophrenia: Is There an Association? A Pilot Study. Schizophr. Res. 2009, 108, 272–279. [Google Scholar] [CrossRef] [PubMed]
  61. Buchanan, A.; Sint, K.; Swanson, J.; Rosenheck, R. Correlates of Future Violence in People Being Treated for Schizophrenia. Am. J. Psychiatry 2019, 176, 694–701. [Google Scholar] [CrossRef]
  62. Keepers, G.A.; Fochtmann, L.J.; Anzia, J.M.; Benjamin, S.; Lyness, J.M.; Mojtabai, R.; Servis, M.; Walaszek, A.; Buckley, P.; Lenzenweger, M.F.; et al. The American Psychiatric Association Practice Guideline for the Treatment of Patients with Schizophrenia. Am. J. Psychiatry 2020, 177, 868–872. [Google Scholar] [CrossRef]
  63. Fazel, S.; Gulati, G.; Linsell, L.; Geddes, J.R.; Grann, M. Schizophrenia and Violence: Systematic Review and Meta-Analysis. PLoS Med. 2009, 6, e1000120. [Google Scholar] [CrossRef]
  64. Krakowski, M.I.; Tural, U.; Czobor, P. Separate Pathways to Violent Behavior in Schizophrenia and in the General Population. J. Psychiatr. Res. 2022, 151, 235–241. [Google Scholar] [CrossRef]
  65. Rund, B.R. A Review of Factors Associated with Severe Violence in Schizophrenia. Nord. J. Psychiatry 2018, 72, 561–571. [Google Scholar] [CrossRef]
  66. Rueve, M.E.; Welton, R.S. Violence and Mental Illness. Psychiatry 2008, 5, 34–48. [Google Scholar]
  67. Radu, M.; Ciucă, A.; Crișan, C.; Pintea, S.; Predescu, E.; Șipos, R.; Moldovan, R.; Băban, A. The Impact of Psychiatric Disorders on Caregivers: An Integrative Predictive Model of Burden, Stigma, and Well-being. Perspect. Psychiatr. Care 2022, 58, 2372–2382. [Google Scholar] [CrossRef] [PubMed]
  68. Fritz, M.; Soravia, S.-M.; Dudeck, M.; Malli, L.; Fakhoury, M. Neurobiology of Aggression—Review of Recent Findings and Relationship with Alcohol and Trauma. Biology 2023, 12, 469. [Google Scholar] [CrossRef] [PubMed]
  69. Mentis, A.-F.A.; Dardiotis, E.; Katsouni, E.; Chrousos, G.P. From Warrior Genes to Translational Solutions: Novel Insights into Monoamine Oxidases (MAOs) and Aggression. Transl. Psychiatry 2021, 11, 130. [Google Scholar] [CrossRef] [PubMed]
  70. Jager, A.; Amiri, H.; Bielczyk, N.; van Heukelum, S.; Heerschap, A.; Aschrafi, A.; Poelmans, G.; Buitelaar, J.K.; Kozicz, T.; Glennon, J.C. Cortical Control of Aggression: GABA Signalling in the Anterior Cingulate Cortex. Eur. Neuropsychopharmacol. 2020, 30, 5–16. [Google Scholar] [CrossRef]
  71. David, S.; Heesink, L.; Geuze, E.; Gladwin, T.; van Honk, J.; Kleber, R.; Leemans, A. Regions of White Matter Abnormalities in the Arcuate Fasciculus in Veterans with Anger and Aggression Problems. Brain Struct. Funct. 2020, 225, 1401–1411. [Google Scholar] [CrossRef]
  72. Gallucci, A.; Riva, P.; Romero Lauro, L.J.; Bushman, B.J. Stimulating the Ventrolateral Prefrontal Cortex (VLPFC) Modulates Frustration-Induced Aggression: A TDCS Experiment. Brain Stimul. 2020, 13, 302–309. [Google Scholar] [CrossRef]
  73. Wong, T.Y.; Sid, A.; Wensing, T.; Eickhoff, S.B.; Habel, U.; Gur, R.C.; Nickl-Jockschat, T. Neural Networks of Aggression: ALE Meta-Analyses on Trait and Elicited Aggression. Brain Struct. Funct. 2019, 224, 133–148. [Google Scholar] [CrossRef]
  74. Romero-Martínez, Á.; González, M.; Lila, M.; Gracia, E.; Martí-Bonmatí, L.; Alberich-Bayarri, Á.; Maldonado-Puig, R.; Ten-Esteve, A.; Moya-Albiol, L. The Brain Resting-State Functional Connectivity Underlying Violence Proneness: Is It a Reliable Marker for Neurocriminology? A Systematic Review. Behav. Sci. 2019, 9, 11. [Google Scholar] [CrossRef]
  75. Tomoda, A.; Sheu, Y.-S.; Rabi, K.; Suzuki, H.; Navalta, C.P.; Polcari, A.; Teicher, M.H. Exposure to Parental Verbal Abuse Is Associated with Increased Gray Matter Volume in Superior Temporal Gyrus. Neuroimage 2011, 54, S280–S286. [Google Scholar] [CrossRef]
  76. Cupaioli, F.A.; Zucca, F.A.; Caporale, C.; Lesch, K.-P.; Passamonti, L.; Zecca, L. The Neurobiology of Human Aggressive Behavior: Neuroimaging, Genetic, and Neurochemical Aspects. Prog. Neuro-Psychopharmacol. Biol. Psychiatry 2021, 106, 110059. [Google Scholar] [CrossRef]
  77. Klaus, J.; Wolfs, E.M.; Schutter, D.J. Cerebellar Roots of Aggression in Violent Psychopathic Offenders: Evidence from Structural Neuroimaging Studies. Curr. Opin. Behav. Sci. 2024, 55, 101333. [Google Scholar] [CrossRef]
  78. Heesink, L.; Edward Gladwin, T.; Terburg, D.; van Honk, J.; Kleber, R.; Geuze, E. Proximity Alert! Distance Related Cuneus Activation in Military Veterans with Anger and Aggression Problems. Psychiatry Res. Neuroimaging 2017, 266, 114–122. [Google Scholar] [CrossRef] [PubMed]
  79. Buades-Rotger, M.; Brunnlieb, C.; Münte, T.F.; Heldmann, M.; Krämer, U.M. Winning Is Not Enough: Ventral Striatum Connectivity during Physical Aggression. Brain Imaging Behav. 2016, 10, 105–114. [Google Scholar] [CrossRef] [PubMed]
  80. Wong, L.C.; Wang, L.; D’Amour, J.A.; Yumita, T.; Chen, G.; Yamaguchi, T.; Chang, B.C.; Bernstein, H.; You, X.; Feng, J.E.; et al. Effective Modulation of Male Aggression through Lateral Septum to Medial Hypothalamus Projection. Curr. Biol. 2016, 26, 593–604. [Google Scholar] [CrossRef]
  81. Mahadevia, D.; Saha, R.; Manganaro, A.; Chuhma, N.; Ziolkowski-Blake, A.; Morgan, A.A.; Dumitriu, D.; Rayport, S.; Ansorge, M.S. Dopamine Promotes Aggression in Mice via Ventral Tegmental Area to Lateral Septum Projections. Nat. Commun. 2021, 12, 6796. [Google Scholar] [CrossRef]
  82. Chang, C.-H.; Gean, P.-W. The Ventral Hippocampus Controls Stress-Provoked Impulsive Aggression through the Ventromedial Hypothalamus in Post-Weaning Social Isolation Mice. Cell Rep. 2019, 28, 1195–1205.e3. [Google Scholar] [CrossRef]
  83. Gouveia, F.V.; Hamani, C.; Fonoff, E.T.; Brentani, H.; Alho, E.J.L.; de Morais, R.M.C.B.; de Souza, A.L.; Rigonatti, S.P.; Martinez, R.C.R. Amygdala and Hypothalamus: Historical Overview with Focus on Aggression. Neurosurgery 2019, 85, 11–30. [Google Scholar] [CrossRef]
  84. Popova, N.K.; Tsybko, A.S.; Naumenko, V.S. The Implication of 5-HT Receptor Family Members in Aggression, Depression and Suicide: Similarity and Difference. Int. J. Mol. Sci. 2022, 23, 8814. [Google Scholar] [CrossRef]
  85. Lukkarinen, L.; Tuisku, J.; Sun, L.; Helin, S.; Karlsson, H.K.; Venetjoki, N.; Salomaa, M.; Rautio, P.; Hirvonen, J.; Lauerma, H.; et al. Aberrant Type 2 Dopamine Receptor Availability in Violent Offenders with Psychopathy. Neuroimage 2024, 297, 120724. [Google Scholar] [CrossRef]
  86. Ruchkin, V.; Koposov, R.; Oreland, L.; Af Klinteberg, B.; Grigorenko, E.L. Dopamine-Related Receptors, Substance Dependence, Behavioral Problems and Personality among Juvenile Delinquents. Personal. Individ. Differ. 2021, 169, 109849. [Google Scholar] [CrossRef]
  87. Suri, D.; Zanni, G.; Mahadevia, D.; Chuhma, N.; Saha, R.; Spivack, S.; Pini, N.; Stevens, G.S.; Ziolkowski-Blake, A.; Simpson, E.H.; et al. Dopamine Transporter Blockade during Adolescence Increases Adult Dopamine Function, Impulsivity, and Aggression. Mol. Psychiatry 2023, 28, 3512–3523. [Google Scholar] [CrossRef] [PubMed]
  88. Chaibi, I.; Bennis, M.; Ba-M’Hamed, S. GABA-A Receptor Signaling in the Anterior Cingulate Cortex Modulates Aggression and Anxiety-Related Behaviors in Socially Isolated Mice. Brain Res. 2021, 1762, 147440. [Google Scholar] [CrossRef] [PubMed]
  89. Peng, S.-X.; Pei, J.; Rinaldi, B.; Chen, J.; Ge, Y.-H.; Jia, M.; Wang, J.; Delahaye-Duriez, A.; Sun, J.-H.; Zang, Y.-Y.; et al. Dysfunction of AMPA Receptor GluA3 Is Associated with Aggressive Behavior in Human. Mol. Psychiatry 2022, 27, 4092–4102. [Google Scholar] [CrossRef]
  90. Felthous, A.R.; Nassif, J. CNS Glutamate in Impulsive Aggression. In Glutamate and Neuropsychiatric Disorders; Pavlovic, Z.M., Ed.; Springer International Publishing: Cham, Switzerland, 2022; pp. 283–311. ISBN 978-3-030-87479-7. [Google Scholar]
  91. Nordman, J.C. Anger Management: Mechanisms of Glutamate Receptor-Mediated Synaptic Plasticity Underlying Animal Aggression. Int. J. Biochem. Cell Biol. 2022, 142, 106120. [Google Scholar] [CrossRef]
  92. Börjesson, A.; Möller, C.; Hagelin, A.; Vicente, V.; Rane, A.; Lehtihet, M.; Dahl, M.-L.; Gårevik, N.; Ekström, L. Male Anabolic Androgenic Steroid Users with Personality Disorders Report More Aggressive Feelings, Suicidal Thoughts, and Criminality. Medicina 2020, 56, 265. [Google Scholar] [CrossRef] [PubMed]
  93. Hauger, L.E.; Havnes, I.A.; Jørstad, M.L.; Bjørnebekk, A. Anabolic Androgenic Steroids, Antisocial Personality Traits, Aggression and Violence. Drug Alcohol Depend. 2021, 221, 108604. [Google Scholar] [CrossRef] [PubMed]
  94. Bertozzi, G.; Sessa, F.; Albano, G.D.; Sani, G.; Maglietta, F.; Roshan, M.H.K.; Volti, G.L.; Bernardini, R.; Avola, R.; Pomara, C.; et al. The Role of Anabolic Androgenic Steroids in Disruption of the Physiological Function in Discrete Areas of the Central Nervous System. Mol. Neurobiol. 2018, 55, 5548–5556. [Google Scholar] [CrossRef] [PubMed]
  95. Christoffersen, T.; Andersen, J.T.; Dalhoff, K.P.; Horwitz, H. Anabolic-Androgenic Steroids and the Risk of Imprisonment. Drug Alcohol Depend. 2019, 203, 92–97. [Google Scholar] [CrossRef]
  96. Sontate, K.V.; Rahim Kamaluddin, M.; Naina Mohamed, I.; Mohamed, R.M.P.; Shaikh, M.F.; Kamal, H.; Kumar, J. Alcohol, Aggression, and Violence: From Public Health to Neuroscience. Front. Psychol. 2021, 12, 699726. [Google Scholar] [CrossRef]
  97. Heinz, A.J.; Beck, A.; Meyer-Lindenberg, A.; Sterzer, P.; Heinz, A. Cognitive and Neurobiological Mechanisms of Alcohol-Related Aggression. Nat. Rev. Neurosci. 2011, 12, 400–413. [Google Scholar] [CrossRef]
  98. van Amsterdam, J.G.C.; Ramaekers, J.G.; Verkes, R.-J.; Kuypers, K.P.C.; Goudriaan, A.E.; van den Brink, W. Alcohol- and Drug-Related Public Violence in Europe. Eur. J. Criminol. 2020, 17, 806–825. [Google Scholar] [CrossRef]
  99. White, A. Gender Differences in the Epidemiology of Alcohol Use and Related Harms in the United States. Alcohol Res. Curr. Rev. 2020, 40, 1. [Google Scholar] [CrossRef] [PubMed]
  100. Bortolato, M.; Braccagni, G.; Pederson, C.A.; Floris, G.; Fite, P.J. “Weeding out” Violence? Translational Perspectives on the Neuropsychobiological Links between Cannabis and Aggression. Aggress. Violent Behav. 2024, 78, 101948. [Google Scholar] [CrossRef] [PubMed]
  101. Moulin, V.; Framorando, D.; Gasser, J.; Dan-Glauser, E. The Link Between Cannabis Use and Violent Behavior in the Early Phase of Psychosis: The Potential Role of Impulsivity. Front. Psychiatry 2022, 13, 746287. [Google Scholar] [CrossRef] [PubMed]
  102. Dellazizzo, L.; Potvin, S.; Athanassiou, M.; Dumais, A. Violence and Cannabis Use: A Focused Review of a Forgotten Aspect in the Era of Liberalizing Cannabis. Front. Psychiatry 2020, 11, 567887. [Google Scholar] [CrossRef]
  103. Callaghan, R.C.; Sanches, M.; Hathaway, A.; Asbridge, M.; Kish, S.J. Canada’s Cannabis Legalization and Adult Crime Patterns, 2015–2021: A Time Series Study. Addict. Behav. 2023, 146, 107813. [Google Scholar] [CrossRef]
  104. Docherty, J.R.; Alsufyani, H.A. Pharmacology of Drugs Used as Stimulants. J. Clin. Pharmacol. 2021, 61, S53–S69. [Google Scholar] [CrossRef]
  105. O’Malley, K.Y.; Hart, C.L.; Casey, S.; Downey, L.A. Methamphetamine, Amphetamine, and Aggression in Humans: A Systematic Review of Drug Administration Studies. Neurosci. Biobehav. Rev. 2022, 141, 104805. [Google Scholar] [CrossRef]
  106. Kuypers, K.P.C.; Verkes, R.J.; van den Brink, W.; van Amsterdam, J.G.C.; Ramaekers, J.G. Intoxicated Aggression: Do Alcohol and Stimulants Cause Dose-Related Aggression? A Review. Eur. Neuropsychopharmacol. 2020, 30, 114–147. [Google Scholar] [CrossRef]
  107. Sayrafizadeh, N.; Ledwos, N.; Husain, M.I.; Castle, D.J. Aggressive Behaviours Associated with MDMA and Psychedelics: A Narrative Review. Acta Neuropsychiatr. 2024, 1–13. [Google Scholar] [CrossRef]
  108. Pepe, M.; Di Nicola, M.; Cocciolillo, F.; Chiappini, S.; Martinotti, G.; Calcagni, M.L.; Sani, G. 3-Methoxy-Phencyclidine Induced Psychotic Disorder: A Literature Review and an 18F-FDG PET/CT Case Report. Pharmaceuticals 2024, 17, 452. [Google Scholar] [CrossRef] [PubMed]
  109. Javitt, D.C.; Avissar, M. Disorders Due to Substance Use: Phencyclidine. In Tasman’s Psychiatry; Springer International Publishing: Cham, Switzerland, 2023; pp. 1–19. [Google Scholar]
  110. Ciucă Anghel, D.-M.; Nițescu, G.V.; Tiron, A.-T.; Guțu, C.M.; Baconi, D.L. Understanding the Mechanisms of Action and Effects of Drugs of Abuse. Molecules 2023, 28, 4969. [Google Scholar] [CrossRef] [PubMed]
  111. Maremmani, I.; Avella, M.T.; Novi, M.; Bacciardi, S.; Maremmani, A.G.I. Aggressive Behavior and Substance Use Disorder: The Heroin Use Disorder as a Case Study. Addict. Disord. Their Treat. 2020, 19, 161–173. [Google Scholar] [CrossRef]
  112. Hansen, C.C.; Ljung, H.; Brodtkorb, E.; Reimers, A. Mechanisms Underlying Aggressive Behavior Induced by Antiepileptic Drugs: Focus on Topiramate, Levetiracetam, and Perampanel. Behav. Neurol. 2018, 2018, 2064027. [Google Scholar] [CrossRef] [PubMed]
  113. Steinhoff, B.J.; Klein, P.; Klitgaard, H.; Laloyaux, C.; Moseley, B.D.; Ricchetti-Masterson, K.; Rosenow, F.; Sirven, J.I.; Smith, B.; Stern, J.M.; et al. Behavioral Adverse Events with Brivaracetam, Levetiracetam, Perampanel, and Topiramate: A Systematic Review. Epilepsy Behav. 2021, 118, 107939. [Google Scholar] [CrossRef]
  114. Strzelczyk, A.; Schubert-Bast, S. Psychobehavioural and Cognitive Adverse Events of Anti-Seizure Medications for the Treatment of Developmental and Epileptic Encephalopathies. CNS Drugs 2022, 36, 1079–1111. [Google Scholar] [CrossRef]
  115. Trenton, A.J.; Currier, G.W. Behavioural Manifestations of Anabolic Steroid Use. CNS Drugs 2005, 19, 571–595. [Google Scholar] [CrossRef]
  116. Currie, A.; McDuff, D.; Johnston, A.; Hopley, P.; Hitchcock, M.E.; Reardon, C.L.; Hainline, B. Management of Mental Health Emergencies in Elite Athletes: A Narrative Review. Br. J. Sports Med. 2019, 53, 772–778. [Google Scholar] [CrossRef]
  117. Jung, Y.; Namkoong, K. Alcohol. In Handbook of Clinical Neurology; Elsevier B.V.: Amsterdam, The Netherlands, 2014; Volume 125, pp. 115–121. [Google Scholar]
  118. Bui, Q.M.; Simpson, S.; Nordstrom, K. Psychiatric and Medical Management of Marijuana Intoxication in the Emergency Department. West. J. Emerg. Med. 2015, 16, 414–417. [Google Scholar] [CrossRef]
  119. Kreis, I.; Lagerberg, T.V.; Wold, K.F.; Åsbø, G.; Simonsen, C.; Flaaten, C.B.; Engen, M.J.; Lyngstad, S.H.; Widing, L.H.; Ueland, T.; et al. Behind the Heterogeneity in the Long-Term Course of First-Episode Psychosis: Different Psychotic Symptom Trajectories Are Associated with Different Patterns of Cannabis and Stimulant Use. Schizophr. Res. 2024, 271, 91–99. [Google Scholar] [CrossRef]
  120. Nishiguchi, M.; Nishio, H. Forensic Toxicology of Stimulants and Psychotropic Drugs. In Current Human Cell Research and Applications; Ishikawa, T., Ed.; Springer: Singapore, 2019; pp. 65–81. ISBN 978-981-13-2296-9. [Google Scholar]
  121. Waters, K. Pharmacologic Similarities and Differences Among Hallucinogens. J. Clin. Pharmacol. 2021, 61, S100–S113. [Google Scholar] [CrossRef] [PubMed]
  122. McGovern, H.T.; Grimmer, H.J.; Doss, M.K.; Hutchinson, B.T.; Timmermann, C.; Lyon, A.; Corlett, P.R.; Laukkonen, R.E. An Integrated Theory of False Insights and Beliefs under Psychedelics. Commun. Psychol. 2024, 2, 69. [Google Scholar] [CrossRef] [PubMed]
  123. Bey, T.; Patel, A. Phencyclidine Intoxication and Adverse Effects: A Clinical and Pharmacological Review of an Illicit Drug. Calif. J. Emerg. Med. 2007, 8, 9–14. [Google Scholar]
  124. Maremmani, A.G.I.; Rovai, L.; Rugani, F.; Pacini, M.; Lamanna, F.; Bacciardi, S.; Perugi, G.; Deltito, J.; Dell’Osso, L.; Maremmani, I. Correlations Between Awareness of Illness (Insight) and History of Addiction in Heroin-Addicted Patients. Front. Psychiatry 2012, 3, 61. [Google Scholar] [CrossRef] [PubMed]
  125. Bowers, L.; Brennan, G.; Ransom, S.; Winship, G.; Theodoridou, C. The Nursing Observed Illness Intensity Scale (NOIIS). J. Psychiatr. Ment. Health Nurs. 2011, 18, 28–34. [Google Scholar] [CrossRef]
  126. Silva, E. The HCR-20 and Violence Risk Assessment—Will a Peak of Inflated Expectations Turn to a Trough of Disillusionment? BJPsych Bull. 2020, 44, 269–271. [Google Scholar] [CrossRef]
  127. Webster, C.D.; Nicholls, T.L.; Martin, M.; Desmarais, S.L.; Brink, J. Short-Term Assessment of Risk and Treatability (START): The Case for a New Structured Professional Judgment Scheme. Behav. Sci. Law 2006, 24, 747–766. [Google Scholar] [CrossRef]
  128. Harris, G.T.; Rice, M.E.; Quinsey, V.L. Violent Recidivism of Mentally Disordered Offenders: The Development of a Statistical Prediction Instrument. Crim. Justice Behav. 1993, 20, 315–335. [Google Scholar] [CrossRef]
  129. Hare, R.D. The Hare Psychopathy Checklist—Revised, 2nd ed.; Multi-Health Systems: Toronto, ON, Canada, 2003. [Google Scholar]
  130. Dolan, M.; Fullam, R. The Validity of the Violence Risk Scale Second Edition (VRS-2) in a British Forensic Inpatient Sample. J. Forens. Psychiatry Psychol. 2007, 18, 381–393. [Google Scholar] [CrossRef]
  131. Loza, W.; Green, K. The Self-Appraisal Questionnaire. J. Interpers. Violence 2003, 18, 781–797. [Google Scholar] [CrossRef]
  132. Monahan, J.; Steadman, H.J.; Appelbaum, P.S.; Grisso, T.; Mulvey, E.P.; Roth, L.H.; Robbins, P.C.; Banks, S.; Silver, E. The Classification of Violence Risk. Focus 2019, 17, 429. [Google Scholar] [CrossRef] [PubMed]
  133. Smith, K.J.; Macpherson, G.; O’Rourke, S.; Kelly, C. The Relationship between Insight and Violence in Psychosis: A Systematic Literature Review. J. Forens. Psychiatry Psychol. 2020, 31, 183–221. [Google Scholar] [CrossRef]
  134. Schandrin, A.; Norton, J.; Raffard, S.; Aouizerate, B.; Berna, F.; Brunel, L.; Chereau-Boudet, I.; D’Amato, T.; Denizot, H.; Dubertret, C.; et al. A Multi-Dimensional Approach to the Relationship between Insight and Aggressiveness in Schizophrenia: Findings from the FACE-SZ Cohort. Schizophr. Res. 2019, 204, 38–45. [Google Scholar] [CrossRef] [PubMed]
  135. Fischer-Vieler, T.; Ringen, P.A.; Kvig, E.; Bell, C.; Hjell, G.; Tesli, N.; Rokicki, J.; Melle, I.; Andreassen, O.A.; Friestad, C.; et al. Associations Between Clinical Insight and History of Severe Violence in Patients with Psychosis. Schizophr. Bull. Open 2023, 4, sgad011. [Google Scholar] [CrossRef] [PubMed]
  136. Polat, H.; Uğur, K.; Aslanoğlu, E.; Yıldız, S.; Yagin, F.H. The Effect of Functional Remission and Cognitive Insight on Criminal Behavior in Patients with Schizophrenia. Arch. Psychiatr. Nurs. 2023, 45, 176–183. [Google Scholar] [CrossRef]
  137. Lamsma, J.; Harte, J.M. Violence in Psychosis: Conceptualizing Its Causal Relationship with Risk Factors. Aggress. Violent Behav. 2015, 24, 75–82. [Google Scholar] [CrossRef]
  138. González-Ortega, I.; Mosquera, F.; Echeburúa, E.; González-Pinto, A. Insight, Psychosis and Aggressive Behaviour in Mania. Eur. J. Psychiatry 2010, 24, 70–77. [Google Scholar] [CrossRef]
  139. Luo, C.; Chen, H.; Zhong, S.; Guo, H.; Li, Q.; Cai, W.; de Girolamo, G.; Zhou, J.; Wang, X. Manic Episode, Aggressive Behavior and Poor Insight Are Significantly Associated with Involuntary Admission in Patients with Bipolar Disorders. PeerJ 2019, 7, e7339. [Google Scholar] [CrossRef]
  140. Pompili, E.; Carlone, C.; Silvestrini, C.; Nicolò, G. Focus on Aggressive Behaviour in Mental Illness. Riv. Psichiatr. 2017, 52, 175–179. [Google Scholar] [CrossRef]
  141. Habibi Asgarabad, M.; Ruhollah Hosseini, S.; Salehi Yegaei, P.; Moradi, S.; Lysaker, P.H. Psychopathology and Poor Clinical Insight in Psychotic Patients. J. Nerv. Ment. Dis. 2022, 210, 532–540. [Google Scholar] [CrossRef]
  142. Volavka, J. Violence in Schizophrenia and Bipolar Disorder. Psychiatr. Danub. 2013, 25, 24–33. [Google Scholar] [PubMed]
  143. Witt, K.; van Dorn, R.; Fazel, S. Risk Factors for Violence in Psychosis: Systematic Review and Meta-Regression Analysis of 110 Studies. PLoS ONE 2013, 8, e55942. [Google Scholar] [CrossRef]
  144. Meyer, L.F.; Telles, L.E.d.B.; Mecler, K.; Soares, A.L.A.G.; Alves, R.S.; Valença, A.M. Schizophrenia and Violence: Study in a General Psychiatric Hospital with HCR-20 and MOAS. Trends Psychiatry Psychother. 2018, 40, 310–317. [Google Scholar] [CrossRef] [PubMed]
  145. Chang, W.C.; Chen, E.S.M.; Hui, C.L.M.; Chan, S.K.W.; Lee, E.H.M.; Chen, E.Y.H. Prevalence and Risk Factors for Suicidal Behavior in Young People Presenting with First-Episode Psychosis in Hong Kong: A 3-Year Follow-up Study. Soc. Psychiatry Psychiatr. Epidemiol. 2015, 50, 219–226. [Google Scholar] [CrossRef]
  146. Walsh, E.; Gilvarry, C.; Samele, C.; Harvey, K.; Manley, C.; Tattan, T.; Tyrer, P.; Creed, F.; Murray, R.; Fahy, T. Predicting Violence in Schizophrenia: A Prospective Study. Schizophr. Res. 2004, 67, 247–252. [Google Scholar] [CrossRef]
  147. Swanson, J.W.; Swartz, M.S.; Van Dorn, R.A.; Volavka, J.; Monahan, J.; Stroup, T.S.; McEvoy, J.P.; Wagner, H.R.; Elbogen, E.B.; Lieberman, J.A. Comparison of Antipsychotic Medication Effects on Reducing Violence in People with Schizophrenia. Br. J. Psychiatry 2008, 193, 37–43. [Google Scholar] [CrossRef]
  148. Swanson, J.W.; Swartz, M.S.; Van Dorn, R.A.; Elbogen, E.B.; Wagner, H.R.; Rosenheck, R.A.; Stroup, T.S.; McEvoy, J.P.; Lieberman, J.A. A National Study of Violent Behavior in Persons with Schizophrenia. Arch. Gen. Psychiatry 2006, 63, 490. [Google Scholar] [CrossRef]
  149. Stompe, T.; Ortwein-Swoboda, G.; Schanda, H. Schizophrenia, Delusional Symptoms, and Violence: The Threat/Control-Override Concept Reexamined. Schizophr. Bull. 2004, 30, 31–44. [Google Scholar] [CrossRef]
  150. Whiting, D.; Lichtenstein, P.; Fazel, S. Violence and Mental Disorders: A Structured Review of Associations by Individual Diagnoses, Risk Factors, and Risk Assessment. Lancet Psychiatry 2021, 8, 150–161. [Google Scholar] [CrossRef]
  151. Moran, P.; Walsh, E.; Tyrer, P.; Burns, T.; Creed, F.; Fahy, T. Impact of Comorbid Personality Disorder on Violence in Psychosis. Br. J. Psychiatry 2003, 182, 129–134. [Google Scholar] [CrossRef]
  152. Schanda, H. Untersuchungen Zur Frage Des Zusammenhangs Zwischen Psychosen Und Kriminalität/Gewalttätigkeit. Fortschritte Neurol. Psychiatr. 2006, 74, 85–100. [Google Scholar] [CrossRef] [PubMed]
  153. Yoshikawa, K.; Taylor, P.J.; Yamagami, A.; Okada, T.; Ando, K.; Taruya, T.; Matsumoto, T.; Kikuchi, A. Violent Recidivism among Mentally Disordered Offenders in Japan. Crim. Behav. Ment. Health 2007, 17, 137–151. [Google Scholar] [CrossRef] [PubMed]
  154. Kosger, F.; Essizoglu, A.; Sonmez, I.; Gulec, G.; Genek, M.; Akarsu, O. The Relationship between Violence and Insight and Cognitive Functions in Patients with Schizophrenia. Turkish J. Psychiatry 2015, 26. [Google Scholar] [CrossRef]
  155. Fazel, S.; Buxrud, P.; Ruchkin, V.; Grann, M. Homicide in Discharged Patients with Schizophrenia and Other Psychoses: A National Case-Control Study. Schizophr. Res. 2010, 123, 263–269. [Google Scholar] [CrossRef]
  156. Steinert, T. Prediction of Inpatient Violence. Acta Psychiatr. Scand. 2002, 106, 133–141. [Google Scholar] [CrossRef]
  157. Ekinci, O.; Ekinci, A. Association between Insight, Cognitive Insight, Positive Symptoms and Violence in Patients with Schizophrenia. Nord. J. Psychiatry 2013, 67, 116–123. [Google Scholar] [CrossRef]
  158. Rozalski, V.; McKeegan, G.M. Insight and Symptom Severity in an Inpatient Psychiatric Sample. Psychiatr. Q. 2019, 90, 339–350. [Google Scholar] [CrossRef]
  159. Galletti, C.; Paolini, E.; Tortorella, A.; Compton, M.T. Auditory and Non-Auditory Hallucinations in First-Episode Psychosis: Differential Associations with Diverse Clinical Features. Psychiatry Res. 2017, 254, 268–274. [Google Scholar] [CrossRef]
  160. Umut, G.; Öztürk Altun, Z.; Danışmant, B.S.; Küçükparlak, İ.; Karamustafalıoğlu, N. Bir Eğitim Hastanesinde Yatarak Tedavi Gören Şizofreni Hastalarında Tedavi Uyumu, Içgörü ve Agresyon Ilişkisi / Relationship between Treatment Adherence, Insight and Violence among Schizophrenia Inpatients in a Training Hospital Sample. Dusunen Adam J. Psychiatry Neurol. Sci. 2012, 25, 212–220. [Google Scholar] [CrossRef]
  161. Volavka, J.; Van Dorn, R.A.; Citrome, L.; Kahn, R.S.; Fleischhacker, W.W.; Czobor, P. Hostility in Schizophrenia: An Integrated Analysis of the Combined Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) and the European First Episode Schizophrenia Trial (EUFEST) Studies. Eur. Psychiatry 2016, 31, 13–19. [Google Scholar] [CrossRef]
  162. Jónsdóttir, H.; Opjordsmoen, S.; Birkenaes, A.B.; Simonsen, C.; Engh, J.A.; Ringen, P.A.; Vaskinn, A.; Friis, S.; Sundet, K.; Andreassen, O.A. Predictors of Medication Adherence in Patients with Schizophrenia and Bipolar Disorder. Acta Psychiatr. Scand. 2013, 127, 23–33. [Google Scholar] [CrossRef] [PubMed]
  163. Siserman, C.; Delcea, C.; Gyorgy, M.; Crisan, C. Forensic Perspective of the COVID Pandemic Impact on the Number of Victims of Violence. Rom. J. Leg. Med. 2022, 30, 8–11. [Google Scholar] [CrossRef]
  164. Whiteman, P.J.; Macias-Konstantopoulos, W.L.; Relan, P.; Knopov, A.; Ranney, M.L.; Riviello, R.J. Violence and Abuse: A Pandemic Within a Pandemic. West. J. Emerg. Med. 2023, 24, 743–750. [Google Scholar] [CrossRef] [PubMed]
  165. Ramachandran, A.S.; Ramanathan, R.; Praharaj, S.K.; Kanradi, H.; Sharma, P.S.V.N. A Cross-Sectional, Comparative Study of Insight in Schizophrenia and Bipolar Patients in Remission. Indian J. Psychol. Med. 2016, 38, 207–212. [Google Scholar] [CrossRef] [PubMed]
  166. Braw, Y.; Sitman, R.; Sela, T.; Erez, G.; Bloch, Y.; Levkovitz, Y. Comparison of Insight among Schizophrenia and Bipolar Disorder Patients in Remission of Affective and Positive Symptoms: Analysis and Critique. Eur. Psychiatry 2012, 27, 612–618. [Google Scholar] [CrossRef]
  167. Huang, S.-S.; Chang, C.-C. Comparison of Insight in Patients with Schizophrenia, Bipolar I Disorder, and Major Depressive Disorder in a Real-World Setting. Taiwan J. Psychiatry 2019, 33, 92. [Google Scholar] [CrossRef]
  168. Varga, M.; Magnusson, A.; Flekkøy, K.; David, A.S.; Opjordsmoen, S. Clinical and Neuropsychological Correlates of Insight in Schizophrenia and Bipolar I Disorder: Does Diagnosis Matter? Compr. Psychiatry 2007, 48, 583–591. [Google Scholar] [CrossRef]
  169. Robertson, A.G.; Swanson, J.W.; Frisman, L.K.; Lin, H.; Swartz, M.S. Patterns of Justice Involvement Among Adults with Schizophrenia and Bipolar Disorder: Key Risk Factors. Psychiatr. Serv. 2014, 65, 931–938. [Google Scholar] [CrossRef]
  170. Muir-Cochrane, E.; Oster, C.; Gerace, A.; Dawson, S.; Damarell, R.; Grimmer, K. The Effectiveness of Chemical Restraint in Managing Acute Agitation and Aggression: A Systematic Review of Randomized Controlled Trials. Int. J. Ment. Health Nurs. 2020, 29, 110–126. [Google Scholar] [CrossRef]
  171. Howner, K.; Andiné, P.; Engberg, G.; Ekström, E.H.; Lindström, E.; Nilsson, M.; Radovic, S.; Hultcrantz, M. Pharmacological Treatment in Forensic Psychiatry—A Systematic Review. Front. Psychiatry 2020, 10, 963. [Google Scholar] [CrossRef]
  172. Bartsch, C.J.; Nordman, J.C. Promises and Pitfalls of NMDA Receptor Antagonists in Treating Violent Aggression. Front. Behav. Neurosci. 2022, 16, 938044. [Google Scholar] [CrossRef]
  173. Slamanig, R.; Reisegger, A.; Winkler, H.; de Girolamo, G.; Carrà, G.; Crocamo, C.; Fangerau, H.; Markiewicz, I.; Heitzman, J.; Salize, H.J.; et al. A Systematic Review of Non-Pharmacological Strategies to Reduce the Risk of Violence in Patients with Schizophrenia Spectrum Disorders in Forensic Settings. Front. Psychiatry 2021, 12, 618860. [Google Scholar] [CrossRef]
  174. Kuivalainen, S.; Vehviläinen-Julkunen, K.; Louheranta, O.; Putkonen, A.; Repo-Tiihonen, E.; Tiihonen, J. De-escalation Techniques Used, and Reasons for Seclusion and Restraint, in a Forensic Psychiatric Hospital. Int. J. Ment. Health Nurs. 2017, 26, 513–524. [Google Scholar] [CrossRef]
  175. Johnston, I.; Price, O.; McPherson, P.; Armitage, C.J.; Brooks, H.; Bee, P.; Lovell, K.; Brooks, C.P. De-Escalation of Conflict in Forensic Mental Health Inpatient Settings: A Theoretical Domains Framework-Informed Qualitative Investigation of Staff and Patient Perspectives. BMC Psychol. 2022, 10, 30. [Google Scholar] [CrossRef]
  176. Brenig, D.; Gade, P.; Voellm, B. Is Mental Health Staff Training in De-Escalation Techniques Effective in Reducing Violent Incidents in Forensic Psychiatric Settings?—A Systematic Review of the Literature. BMC Psychiatry 2023, 23, 246. [Google Scholar] [CrossRef]
  177. Velligan, D.I.; Sajatovic, M.; Hatch, A.; Kramata, P.; Docherty, J. Why Do Psychiatric Patients Stop Antipsychotic Medication? A Systematic Review of Reasons for Nonadherence to Medication in Patients with Serious Mental Illness. Patient Prefer. Adherence 2017, 11, 449–468. [Google Scholar] [CrossRef]
  178. Loots, E.; Goossens, E.; Vanwesemael, T.; Morrens, M.; Van Rompaey, B.; Dilles, T. Interventions to Improve Medication Adherence in Patients with Schizophrenia or Bipolar Disorders: A Systematic Review and Meta-Analysis. Int. J. Environ. Res. Public Health 2021, 18, 10213. [Google Scholar] [CrossRef]
  179. Kane, J.M.; Kishimoto, T.; Correll, C.U. Non-Adherence to Medication in Patients with Psychotic Disorders: Epidemiology, Contributing Factors and Management Strategies. World Psychiatry 2013, 12, 216–226. [Google Scholar] [CrossRef]
  180. Haddad, P.; Brain, C.; Scott, J. Nonadherence with Antipsychotic Medication in Schizophrenia: Challenges and Management Strategies. Patient Relat. Outcome Meas. 2014, 2014, 43–62. [Google Scholar] [CrossRef]
  181. U.S. Food & Drug Administration. FDA Approves Pill with Sensor That Digitally Tracks If Patients Have Ingested Their Medication. Available online: https://www.fda.gov/news-events/press-announcements/fda-approves-pill-sensor-digitally-tracks-if-patients-have-ingested-their-medication (accessed on 10 September 2024).
  182. Alipour, A.; Gabrielson, S.; Patel, P.B. Ingestible Sensors and Medication Adherence: Focus on Use in Serious Mental Illness. Pharmacy 2020, 8, 103. [Google Scholar] [CrossRef]
  183. de Miguel Beriain, I.; Morla González, M. ‘Digital Pills’ for Mental Diseases: An Ethical and Social Analysis of the Issues behind the Concept. J. Law Biosci. 2020, 7, lsaa040. [Google Scholar] [CrossRef]
  184. Swartz, A.K.; Friesen, P. The First Smart Pill: Digital Revolution or Last Gasp? Kennedy Inst. Ethics J. 2023, 33, 277–319. [Google Scholar] [CrossRef]
  185. Fiorillo, A.; Barlati, S.; Bellomo, A.; Corrivetti, G.; Nicolò, G.; Sampogna, G.; Stanga, V.; Veltro, F.; Maina, G.; Vita, A. The Role of Shared Decision-Making in Improving Adherence to Pharmacological Treatments in Patients with Schizophrenia: A Clinical Review. Ann. Gen. Psychiatry 2020, 19, 43. [Google Scholar] [CrossRef]
Figure 1. Classification of the levels of association of different factors with violent behavior (from the findings presented by Witt et al. [143]).
Figure 1. Classification of the levels of association of different factors with violent behavior (from the findings presented by Witt et al. [143]).
Psychiatryint 05 00067 g001
Table 1. Most common insight scales with each scale’s number of items and definitory traits.
Table 1. Most common insight scales with each scale’s number of items and definitory traits.
Name of the ScaleNo. Insight ItemsType
Present State Examination (PSE)1General scale (not specific for insight)
Positive and Negative Syndrome Scale (PANSS)—insight item1
Birchwood Insight Scale (BIS)8Scales for assessing clinical insight
Schedule for the Assessment of Insight—Expanded (SAI-E)11
Insight and Treatment Attitude Questionnaire (ITAQ)11
Insight Scale (Markova and Berrios, second version, 2002) (IS)30
Scale to Assess Unawareness of Mental Disorders (SUMD)74
Beck Cognitive Insight Scale (BCIS)15Cognitive insight
Insight Scale for Affective Disorders (ISAD)17Insight in affective disorders
Table 2. Aspects of clinical insight assessed by different instruments.
Table 2. Aspects of clinical insight assessed by different instruments.
Assessed Dimension of InsightBISITAQSAI-EISSUMD
Acceptance of the illness labelXXXXX
Awareness of having a mental disorderX XXX
Perceived need for treatmentXXX
Awareness of the benefits of treatment X
Attribution of benefits to the treatment X X
Awareness of signs and symptomsX XXX
Attribution of signs and symptoms to having a mental disorderX XXX
Relabeling psychotic experiences correctlyX XX
Awareness of the social consequences of having a mental disorder X X
Awareness of emotional/psychological changes XX
Temporal Aspects
Assessed present insightXXXXX
Assessed insight for past periods X X
Patient’s prediction for the future X
Table 3. Brain regions and structures involved in the mediation of aggressive behavior.
Table 3. Brain regions and structures involved in the mediation of aggressive behavior.
RegionStructureFunctionReference
Frontal lobeAnterior cingulate cortexPart of the top-down circuitry that mediates reactive aggression.[70]
Prefrontal white matterConnectivity between emotion-processing, inhibitory, and value-processing brain regions.[71]
Prefrontal cortexTop-down control over subcortical regions involved in processing threatening stimuli.[72]
Orbitofrontal cortexPart of the top-down circuitry that mediates reactive aggression.[70]
Parietal lobePrecuneusInvolved in self-consciousness and self-referential processes.[73]
Angular gyrusPart of the brain networks underlying moral reasoning; anger expression facilitating projections with limbic structures.[74]
Temporal lobeSuperior temporal gyrusLanguage and speech processing; alterations observed during parental verbal abuse.[75]
Temporoparietal junctionPart of the structures important for moral behavior.[76]
Temporal white matterConnectivity in the frontotemporal, limbic, and paralimbic brain regions.[77]
Occipital lobeCuneusMotivational attention—perceptual processing of motivationally relevant stimuli (e.g., proximity).[78]
Limbic systemStriatumReward processing. Activation of ventral striatum has been observed in desires of revenge.[79]
SeptumThe lateral septum influences the activities of attack-related cells in the medial hypothalamus.[80]
Ventral tegmental areaPromotes aggression and establishes baseline aggression through dopaminergic neurons projecting to the lateral septum.[81]
HippocampusThe dorsal hippocampus is involved in spatial memory. The ventral hippocampus is involved in emotions, motivation, and defensive behavior regulation.[82]
HypothalamusControls homeostasis and motivated behaviors.[83]
AmygdalaProcessing threatening stimuli; autonomic, neuroendocrine, and behavioral response mediation.[83]
Table 4. Summary of the drugs possibly associated with increased aggressive and violent behavior.
Table 4. Summary of the drugs possibly associated with increased aggressive and violent behavior.
SubstanceRelation to InsightMechanismPsychiatric SymptomsReferences
AASsAssociated with poor judgementEnhance the activation of D2 receptors from supraoptic neurons onto hypothalamus; stimulate 5-HT2A receptors in hypothalamus; increase excitatory neurotransmission.Aggressiveness, anxiety, sleeping disorders, mood disorders[92,93,94,115,116]
AlcoholImpairs judgement and insightAcute intake—inhibition of PFC and stimulation of dopamine release in striatum; chronic intake—impairment of serotonin neurotransmission in PFC and amygdala.Aggressiveness, temporary anterograde amnesia, sleeping disorders[97,117]
CannabisImpairs insightModulation of CB1 receptors in GABAergic and glutamatergic neurons; modulation of GABA and glutamate release.Psychosis, schizophrenia, depression, anxiety[100,101,118,119]
StimulantsImpairs insightEnhance release of dopamine, norepinephrine, and serotonin.Psychosis, schizophrenia, anxiety, insomnia[119,120]
Hallucinogens and empathogensCapable of inducing false insightsAgonists of 5-HT2A receptors.Perceptual effects, depersonalization, distortions, illusions, perceptual intensifications, hallucinations[121,122]
NMDA receptor antagonistsNo available dataAntagonize the NMDA receptors.Psychosis, schizophrenia, catatonia[108,109,123]
HeroinImpairs insightOpioid agonist.Addiction[110,124]
AnticonvulsantsNo available dataInhibition of AMPA receptors and alterations in serotonin and GABA levels.Aggressiveness, irritability, anger, insomnia, mood swings, suicidal behavior[112,113,114]
Table 5. Summary of the violence risk scales.
Table 5. Summary of the violence risk scales.
Name of the ScaleNo. ItemsScore/ItemRating
Broset Violence Checklist (BVC)60 → 10—low risk
1–2—moderate risk
>2—increased risk
Dynamic Appraisal for Situational Aggression (DASA)70 → 10—low risk
2–3—moderate risk
>4—increased risk
Modified Overt Aggression Scale (MOAS)40 → 4Higher score → increased risk
Nursing Observed Illness Intensity Score (NOISS)5As a “temperature scale”
Historical, Clinical, and Risk Management 20 (HCR-20)200 → 3Higher score → increased risk
Short-Term Assessment of Risk and Treatability (START)200 → 2 on strength/vulnerability7 risk estimates (low/moderate/severe)
Violence Risk Appraisal Guide—Revised (VRAG-R)12−7 → +6 (depends on item)Higher score → increased risk
Violence Risk Scale Second Version (VRS-2)260 → 3Higher score → increased risk
The Psychopathy Checklist Revised (PCR-R)200 → 2Cut-off: 30 in US; 25 in UK
Self-Appraisal Questionnaire (SAQ)72True/FalseHigher score → increased risk
Table 6. Aspects assessed by interview—observation scales.
Table 6. Aspects assessed by interview—observation scales.
Investigated AspectBVCDASAMOASNOIIS
Irritability/easily angered when requests are deniedXX
AgitationX X
Distress X
ConfusionX
Apathy/withdrawal/negative attitudes X X
Sensitivity to perceived provocation X
Unwillingness to follow directions X
Cognitive accessibility X
Conflict X
Impulsivity X
Verbal threats/aggressionX X
Physical threats/aggressionX X
Self-aggression X
Aggression towards subjectsX X
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Horgoș, B.-M.; Ungureanu, D.; Crișan, C.-A. Insight and Violence: An Overview of the Possible Link and Treatment Options in Forensic Psychiatric Settings. Psychiatry Int. 2024, 5, 975-998. https://doi.org/10.3390/psychiatryint5040067

AMA Style

Horgoș B-M, Ungureanu D, Crișan C-A. Insight and Violence: An Overview of the Possible Link and Treatment Options in Forensic Psychiatric Settings. Psychiatry International. 2024; 5(4):975-998. https://doi.org/10.3390/psychiatryint5040067

Chicago/Turabian Style

Horgoș, Bianca-Mălina, Daniel Ungureanu, and Cătălina-Angela Crișan. 2024. "Insight and Violence: An Overview of the Possible Link and Treatment Options in Forensic Psychiatric Settings" Psychiatry International 5, no. 4: 975-998. https://doi.org/10.3390/psychiatryint5040067

APA Style

Horgoș, B.-M., Ungureanu, D., & Crișan, C.-A. (2024). Insight and Violence: An Overview of the Possible Link and Treatment Options in Forensic Psychiatric Settings. Psychiatry International, 5(4), 975-998. https://doi.org/10.3390/psychiatryint5040067

Article Metrics

Back to TopTop