Histopathological Gap in Aortic Diseases: A Prospective Analysis
by
, ,
Cosmin Marian Banceu
1,2,3
,
Simona Gurzu
4,5,6,*
,
Catalin-Bogdan Satala
4,
Dana Ghiga
7,
Mihai Halic Neamtu
8,9,
Vladimir Voth
10,
Markus Liebrich
10 and
Horatiu Suciu
2,3,6 1
I.O.S.U.D., George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540139 Targu Mures, Romania
2
Department of Surgery M3, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540139 Targu Mures, Romania
3
Emergency Institute for Cardiovascular Diseases and Transplantation Targu Mures, 540136 Targu Mures, Romania
4
Department of Pathology, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540139 Targu Mures, Romania
5
Research Center for Oncopathology and Translational Medicine (CCOMT), George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania
6
Romanian Academy of Medical Sciences, 030167 Bucharest, Romania
7
Department of Medical Scientific Research Methodology, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540139 Targu Mures, Romania
8
Swiss Federal Institute of Forest, Snow and Landscape Research WSL, 8903 Birmensdorf, Switzerland
9
Institute of Environmental Engineering, ETH Zurich, 8039 Zurich, Switzerland
10
Sana Cardiac Surgery, Herdweg 2, 70174 Stuttgart, Germany
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(20), 15470; https://doi.org/10.3390/ijms242015470
Submission received: 4 September 2023
/
Revised: 8 October 2023
/
Accepted: 16 October 2023
/
Published: 23 October 2023
(This article belongs to the Special Issue Cardiovascular Diseases: Histopathological and Molecular Diagnostics)
Abstract
:Aortic dissection (AD) is a critical cardiovascular condition with the potential for devastating consequences. This study evaluated the histological changes in the aorta wall in patients with AD and aortic aneurysm (AA) who received surgical aortic replacement. Histopathological data showed that modifications of the media layer (p = 0.0197), myxomatous aspect (p = 0.0001), and subendothelial layer degeneration (p = 0.0107) were more frequently seen in AA versus AD samples. Patients with AA were approximately twice as likely to develop histological changes than those with AD (p = 0.0037). Patients with moderate or severe medial degeneration had a higher chance of developing AD (p = 0.0001). Because the histopathological score proved to be a predictor of both in-hospital and overall mortality, its evaluation should become the standard of care in any patients who undergo aortic replacement. Individualized postoperative management might be influenced by the histopathological aspect of the aortic layer.
1. Introduction
Acute aortic dissection (AD) is a life-threatening disease in which the risk of mortality increases by 1% per hour without surgical replacement. The stepwise pathomechanism usually includes rupture of the intima with subsequent rupture of the media and adventitia of the aortic layer [1,2,3]. AD might be anterograde or retrograde and longitudinal or transverse. Longitudinal dissection usually causes several re-entries and exit tears. Transverse dissection conducts the progression of the dissection process at the adventitia until its rupture with extravasation of blood in the aortic lumen. Consequently, transverse dissection is associated with a higher risk of preoperative death [4,5,6,7,8].
How the type of dissection or the histopathological changes might influence the mortality rate is unclear. Although several histological studies have focused on AD, the histogenesis and the predictive value of histological assessment are far from understood. Cystic medial necrosis, described by Erdheim [9], was long considered the starting point of dissection. Other associated events include the degeneration of the vasa vasorum, which has been hypothesized to induce hypoxia and increase the risk of aortic rupture [10]. Osada et al. suggested that the absence of restorative fibrosis with significant collagen concentration and perifocal medial apoptosis is another risk factor for aortic rupture [11].
In this context, the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology, based on studies by Halushka et al., elaborated the principles that can be used for the histological evaluation of medial degeneration. However, this classification requires time to prove its effectiveness and be unanimously accepted by the community [12]. In this framework, the medial degeneration and the lesions of the aortic media layer can be evaluated using hematoxylin–eosin (HE) and other histochemical stains such as trichrome, van Gieson, van Gieson–elastica, and PAS Alcian blue. These might be helpful in assessing medial fibrosis, smooth muscle cell nuclei loss or cell disorganization, laminar medial collapse, elastic fiber thinning, disorganization, fragmentation, and mucoid extracellular matrix accumulation (MEMA) with its subdivisions: interlamellar (MEMA-i) and translamellar (MEMA-t). Based on the aforementioned parameters, medial degeneration can be classified as mild, moderate, or severe [12].
This study aimed to provide an in-depth analysis of the histological assessment of the aortic wall and the impact of histological changes on in-hospital mortality and overall mortality in AD patients who received an ascendant aorta replacement. They were compared to patients who received a replacement for an aortic aneurysm (AA).
2. Results
2.1. Clinicopathological Features and Study Design
Most of the 108 patients included in the study were men (Figure 1). The male:female ratio was 2.6:1 in both groups. Although most of the patients were aged over 55 years, those in the AA group were significantly younger. The hospitalization time was similar for the two groups (Table 1).
The rate of preoperative complications was significantly higher in the AD group but there were no differences regarding the postoperative complications (Table 2).
A significant association was found between AD and in-hospital mortality rate. Patients with AD had a 3.857 times higher risk of in-hospital mortality than those with AA (RR = 3.857, 95% CI: 1.127–13.196, p = 0.0006; Figure 1).
We additionally analyzed whether AD was a risk factor for overall mortality, and a statistically significant association was observed. Patients with AD had a 4.188 times higher risk of death (RR = 4.188, 95% CI: 2.235–7.847, p < 0.0001; Figure 2).
2.2. Histopathological Changes: Description
Under the microscope, severe degeneration (Figure 3) was easily detected on the classic HE stain. To evaluate moderate (Figure 4) or mild degeneration (Figure 5), the use of histochemical stains was necessary. PAS Alcian blue proved useful as the elective stain for mucoid medial change, either MEMA-i or the more severe form, MEMA-t. Medial fibrosis was emphasized with a trichrome stain, and elastic fiber fragmentation and loss were visualized with van Gieson–elastica and trichrome stains (Figure 3, Figure 4 and Figure 5).
2.3. Histopathological Changes: Quantification
MEMA-i was the most common histological degenerative change. A mild degenerative degree was observed only in the AA group (n = 6); no patient had a mild degree in the AD group. A moderate score was more prevalent in the AA samples than the AD samples (n = 24 vs. n = 9), whereas the opposite was true for the severe degenerative degree (n = 26 for the AA group vs. n = 43 for the AD group).
Regarding the MEMA-t parameter, a higher mild degree was observed for the AA group (n = 20) versus the AD group (n = 4). Moderate scores were observed in 79.62% of AD patients compared to 48.00% of AA patients, whereas severe scores were similar for the two groups.
Elastic fragmentation and loss changes were observed with mild scores in 11 patients of the AD group versus 29 of the AA group. More AD patients (n = 37) had a moderate degree than in the AA group (n = 20). Data analysis showed a statistically significant association between AD and the type of elastic fragmentation or loss (p = 0.0011).
A further histological degenerative change analyzed was smooth muscle cell nuclei loss. As shown in Table 3, AA patients had a higher mild degenerative degree (70.27%) compared to AD patients (50.98%), whereas the opposite was true for the mild degree (AD with 45% vs. AA with 27%). A statistically significant association was observed between AD and the severity of smooth muscle cell nuclei loss (p < 0.0001).
Finally, we focused on laminar medial collapse. The AD group exhibited higher mild scores (45.83%) compared to the AA group (60.00%), whereas the opposite was true for the moderate scores (45.83% vs. 35.00%). Regarding the severe scores, the AD group had a slightly higher probability compared to the AA group (8.33% vs. 5%).
The cases were further subdivided based on multifocal and focal changes. Mild multifocal laminar medial collapse occurred in 14 patients (73.68%) in the AD group versus five patients (26.32%) in the AA group. Mild focal changes occurred in eight patients (29.63%) in the AD versus 19 patients (70.37%) in the AA group. Using the risk ratio (RR) of 3.055 (95% CI: 1.317–7.087), patients with AD were over three times more likely to develop laminar medial collapse with mild multifocal changes than patients with AA (Table 4).
Only 7.69% (n = 2) of patients with mild medial degeneration developed AD, in contrast to 92.31% (n = 24) who had AA. The frequency of AD was higher among patients with moderate or severe medial degeneration (Table 5).
Synthesis of the histopathological data showed that patients with AA had milder degeneration of the media and, consequently, a lower frequency of dissection compared with the other group.
In both groups, the histopathological changes observed at the level of the ascending aorta from samples collected during surgical treatment were examined in association with the mortality rate.
Regarding the relationship between predictor variables and the outcome variable, the analysis showed that for each unit increase in the histopathological score (i.e., an increase from mild to moderate or moderate to severe), the odds of in-hospital mortality increased by a factor of 3.073, and the odds of overall mortality increased by a factor of 2.9 (Table 6). A statistically significant link was found between the histopathological score, in-hospital mortality (p = 0.0029), and overall mortality (p = 0.0025; Figure 6).
3. Discussion
Aortic disease risks and predisposing variables are widely understood. This potentially life-threatening condition must be identified and managed promptly to prevent catastrophic consequences [13]. Our study identified clinical characteristics including age over 60 years, male gender, and comorbidities such as bicuspid aortic valve, pericardium effusion, or cardiac tamponade as more prevalent in the AD group than in the AA group. These risk factors might also influence the management of aortic diseases and can impact the mortality rates [1,6].
In patients with aortic disease, the mortality rate at various stages (pre-, peri-, and postoperative) remains high, and the time from diagnosis to treatment does not seem consistently brief [4,14,15]. Although postoperative complications could raise overall mortality, these factors are secondary to the primary cause, which is the rapid development of aortic disease. Complications following surgery did not prove to influence the mortality rate in our study. This data highlights the crucial role of adequate treatment after surgery and the importance of the histopathological score, evaluated in the aortic wall, in predicting evolution. The restant native thoraco-abdominal aorta segments remain vulnerable to the pre-existing risk factors that can influence the mortality rate.
Although it is widely accepted that the tissue of the aorta wall may undergo alterations, how these changes might influence patient outcomes is unclear. The importance of the consensus grading scale established by the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology for daily practice is still poorly understood and needs more research [8,12,16,17].
Despite the unknown impact, it is universally agreed that histological changes influence patient outcomes [18,19]. Our study highlights the potential implications of these changes in mortality rates for patients who had recent surgical procedures for AD or AA.
The deep analysis performed in this study revealed significant differences between the two groups in MEMA-i modifications, with a moderate score for the AA group and a severe score for the AD group. AA samples with significant MEMA-t changes showed mild, moderate, and severe AD scores. Among cases with mild and severe scores for AA and moderate scores for AD, elastic fragmentation and loss of substantial changes were identified. AA with mild scores and AD with moderate or severe scores both influence smooth muscle cell nuclei loss. For minor scores in AA and moderate or severe scores in AD, laminar medial collapse alterations were observed.
Based on these findings, the AD and AA frequencies were positively correlated with the degree of medial degeneration identified under the microscope. AD is more likely to occur due to moderate and severe medial degeneration compared to cases of mild medial degeneration, which is more likely to result in AA. Consequently, medial degeneration is a major risk factor for both AA and AD [20].
Knowing the associated medical conditions of patients with aortic diseases allows us to determine their management before, during, and after surgery and decrease the mortality rate of these complex and life-threatening diseases. However, these conditions can also be correlated with histopathological changes, which are the basis of more detailed immunohistochemical and genetic studies in aortic pathology, including rheumatologic evaluation if the etiology is aortitis [21,22,23,24].
An important issue is the possible link between histological findings and the risk of mortality after an ascendant aortic replacement. Considering the patient’s age, gender, and pre-existing health conditions, as is done for preoperative anticoagulant therapy, might allow the patient’s postoperative management to be individualized to obtain a lower mortality rate [25,26,27,28,29].
To guide efforts to improve patient outcomes and decrease mortality rates, future research should be focused on these potential factors and detecting the fundamental mechanisms of their relationships with overall mortality [30].
The study also highlighted that both in-hospital and overall mortality significantly increased with each degree of histopathological score. This confirms the hypothesis that a relationship exists between histopathological changes and in-hospital and overall mortality rates, although the precise mechanisms leading to the association of the histopathology score with the probability of in-hospital mortality are not yet fully known [4].
The presence of aortic disease increases the risk of death in patients who reveal histopathological changes in intraoperatively harvested aortic tissue. This clinically relevant factor must be considered in the prevention program implemented for patients with this disease. Further studies should be conducted to accurately assess these results and analyze potential disagreements for better real-life application.
The degree to which certain risk factors and comorbidities are involved in aortic diseases is known, whereas others are poorly understood and require investigation [31,32,33,34,35]. Identifying those factors will be important for establishing screening and treatment programs that might prevent the disease’s progression and decrease the possible risk of AD [36].
Limitations
The study was carried out in a single cardiac surgery department. Additionally, the follow-up time of six months after surgery was too short for a proper evaluation of the impact of histopathological changes on long-term survival.
Another limitation is that the reported mortality rate is quite high. The study was conducted in a tertiary center, where patients arrive from six distinct counties, and the time between diagnosis and surgical treatment was prolonged for many patients. Despite all surgical therapeutic efforts, these factors increased the revealed mortality rate.
4. Materials and Methods
Patients with AD hospitalized in the Emergency Unit were included in this study. In all consecutive cases, the ascending aorta segments obtained after surgical replacement were histopathologically examined and compared with those collected from patients who were admitted on an ongoing schedule and underwent surgical replacement for AA.
This prospective study included 108 consecutive patients diagnosed with aortic lesions (AD and AA), who received aortic replacement in a single tertiary cardiac surgery institution between 2019 and 2021. The follow-up time was six months.
Adult patients with AA or AD who submitted a signed informed consent for the surgical intervention and the publication of scientific data were included. The study was conducted following the Declaration of Helsinki and approved annually by the Ethical Committee of the George Emil Palade University of Medicine, Pharmacy, Sciences and Technology, Targu Mures, Romania (resolution 7225/07.10.2019, 878/23.04.2020, and 1359/10.05.2021).
Patients aged under 18 years and adult patients who refused to provide consent were excluded from the study. All data related to the patients were analyzed following ethical standards, and standard surgical operating protocols were applied.
In-hospital mortality refers to patients who died while receiving treatment during hospitalization. Overall mortality corresponds to the mortality rate of patients within the first six months of their follow-up period.
4.1. Histological Assessment
Standard protocols were used for processing the ascending aortic wall samples after 24 h of formalin fixation and then paraffin embedding. Each case was analyzed on HE and used three histologic stains: PAS Alcian, van Gieson–elastica, and trichrome.
Histological samples were assessed using the standards recommended by Halushka et al. [12]. Using as major criteria the presence of mucoid extracellular matrix accumulation (MEMA) with either intralamellar (MEMA-i) or translamellar (MEMA-t) extension, elastic fiber changes (fragmentation and loss), smooth muscle cell changes (nuclei loss and cell disarray), and collagen alteration (laminar medial collapse), based on their severity, the overall medial degeneration was scored as mild (score 1), moderate (score 2), or severe (score 3; Table 7). The histopathological samples were analyzed considering the type of aortic disease (AD or AA) and its microscopic aspects. The differences between the two groups were examined for in-hospital and overall mortality.
4.2. Statistical Tests and Standard Protocols
The statistical analysis included elements of descriptive statistics (frequency, percentage, mean, median, standard deviation) and elements of inferential statistics. The Shapiro-Wilk test was applied to determine the distribution of the analyzed data series. For median comparisons, the Mann Whitney test was applied. Chi-square and Fisher tests were applied to evaluate the relationships between qualitative variables. Furthermore, to quantify the relationship between predictor variables and the outcome variable, we performed a binary logistic regression for binary dependent variables. A p-value of 0.05 was selected as the level of significance. SPSS Statistics 28.0.0 software was used for the analysis.
5. Conclusions
Although the histopathological evaluation of the aortic wall is neglected in many centers, it can be a useful diagnostic tool and a predictor of both in-hospital and overall mortality, with a significant increase in mortality risk for every degree of histopathological score. Multicenter studies are necessary to evaluate the real impact of the histopathological assessment on the postoperative evolution of both AA and AD. Furthermore, developing national registers and rolling out prevention programs is necessary to decrease the mortality rate of patients with AD. Due to the surgical treatment involving a limited aortic segment, histopathological changes have significant clinical importance. Based on the changes revealed by the replaced aorta, a guideline might be elaborated for the follow-up of the patient and prevention of further AD.
Author Contributions
Conceptualization, C.M.B. and S.G.; methodology, C.M.B., C.-B.S., D.G. and H.S.; software, D.G.; validation, S.G., H.S., C.-B.S. and M.H.N.; formal analysis, C.M.B., V.V., M.L. and D.G.; investigation, C.M.B., H.S., and C.-B.S.; data curation, C.M.B. and M.H.N.; writing—C.M.B.; writing—review and editing, C.M.B., S.G., M.H.N. and H.S.; visualization, M.H.N., V.V. and M.L.; supervision, H.S. and S.G.; project administration, C.M.B. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
The data supporting this study’s findings are available from the corresponding author upon request.
Acknowledgments
I express my sincere gratitude to Radu Deac, my scientific supervisor, for his ongoing guidance, support, advice, and encouragement during the research for this project. I am also grateful to him for providing me with a wealth of scientific knowledge about scientific research.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Morgan, M.; Mestres, C.A.; Lavanchy, I.; Gerçek, M.; Van Hemelrijck, M.; Sromicki, J.; Vogt, P.; Reser, D. The impact of age and sex on in hospital outcomes in acute type A aortic dissection surgery. J. Thorac. Dis. 2022, 14, 2011–2021. [Google Scholar] [CrossRef] [PubMed]
- Bawiskar, N.; Kamat, S.; Acharya, S.; Mohale, S.; Kumar, S. Type-A aortic dissection masquerading as acute inferior wall myocardial infarction—A rare case report. Med. Sci. 2022, 26, ms61e2007. [Google Scholar] [CrossRef]
- Yin, Z.Q.; Han, H.; Yan, X.; Zheng, Q.J. Research progress on the pathogenesis of aortic dissection. Curr. Probl. Cardiol. 2022, 48, 101249. [Google Scholar] [CrossRef] [PubMed]
- Evangelista, A.; Rabasa, J.M.; Mosquera, V.X.; Barros, A.; Fernández-Tarrio, R.; Calvo-Iglesias, F.; Ferrera, C.; Rozado, J.; López-Ayerbe, J.; Garrote, C.; et al. Diagnosis, management and mortality in acute aortic syndrome: Results of the Spanish Registry of Acute Aortic Syndrome (RESA-II). Eur. Heart J. Acute Cardiovasc. Care 2018, 7, 602–608. [Google Scholar] [CrossRef] [PubMed]
- Kim, J.; Song, H.C. Role of PET/CT in the Evaluation of Aortic Disease. Chonnam Med. J. 2018, 54, 143–152. [Google Scholar] [CrossRef] [PubMed]
- Berretta, P.; Trimarchi, S.; Patel, H.J.; Gleason, T.G.; Eagle, K.A.; Di Eusanio, M. Malperfusion syndromes in type A aortic dissection: What we have learned from IRAD. J. Vis. Surg. 2018, 4, 65. [Google Scholar] [CrossRef]
- Morello, F.; Santoro, M.; Fargion, A.T.; Grifoni, S.; Nazerian, P. Diagnosis and management of acute aortic syndromes in the emergency department. Intern. Emerg. Med. 2021, 16, 171–181. [Google Scholar] [CrossRef]
- Li, Y.; Zhang, N.; Xu, S.; Fan, Z.; Zhu, J.; Huang, L.; Chen, D.; Sun, Z.; Sun, L. Acute type A aortic intramural hematoma and type A aortic dissection: Correlation between the intimal tear features and pathogenesis. Quant. Imaging. Med. Surg. 2020, 10, 1504–1514. [Google Scholar] [CrossRef]
- Moritz, A.R. Medionecrosis Aortae Idiopathica Cystica. Am. J. Pathol. 1932, 8, 717–734.3. [Google Scholar]
- Yuan, S.M.; Jing, H. Cystic medial necrosis: Pathological findings and clinical implications. Rev. Bras. Cir. Cardiovasc. 2011, 26, 107–115, Erratum in Rev. Bras. Cir. Cardiovasc. 2012, 27, 173. [Google Scholar] [CrossRef]
- Osada, H.; Kyogoku, M.; Matsuo, T.; Kanemitsu, N. Histopathological evaluation of aortic dissection: A comparison of congenital versus acquired aortic wall weakness. Interact. Cardiovasc. Thorac. Surg. 2018, 27, 277–283. [Google Scholar] [CrossRef] [PubMed]
- Halushka, M.K.; Angelini, A.; Bartoloni, G.; Basso, C.; Batoroeva, L.; Bruneval, P.; Buja, L.M.; Butany, J.; D’Amati, G.; Fallon, J.T.; et al. Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association For European Cardiovascular Pathology: II. Noninflammatory degenerative diseases—Nomenclature and diagnostic criteria. Cardiovasc. Pathol. 2016, 25, 247–257. [Google Scholar] [CrossRef] [PubMed]
- Wang, C.; Zhang, L.; Li, T.; Xi, Z.; Wu, H.; Li, D. Surgical treatment of type A acute aortic dissection with cerebral malperfusion: A systematic review. J. Cardiothorac. Surg. 2022, 17, 40. [Google Scholar] [CrossRef] [PubMed]
- Sugiyama, K.; Watanuki, H.; Tochii, M.; Futamura, Y.; Kitagawa, Y.; Makino, S.; Ohashi, W.; Matsuyama, K. Impact of GERAADA score in patients with acute type A aortic dissection. J. Cardiothorac. Surg. 2022, 17, 127. [Google Scholar] [CrossRef] [PubMed]
- Evangelista Masip, A.; Lopez-Sainz, A.; Barros Membrilla, A.J.; Iglesias, F.C.; Ayerbe, J.L.; Molluna, M.A.; Rodríguez, V.X.M.; Montoya, F.A.; Fernández, R.T.; Orodea, A.R.; et al. RESA centres. Spanish Registry of Acute Aortic Syndrome (RESA). Changes in therapeutic management and lower mortality in acute aortic syndrome. Rev. Esp. Cardiol. 2022, 75, 816–824. [Google Scholar] [PubMed]
- Leone, O.; Pacini, D.; Foà, A.; Corsini, A.; Agostini, V.; Corti, B.; Di Marco, L.; Leone, A.; Lorenzini, M.; Reggiani, L.B.; et al. Redefining the histopathologic profile of acute aortic syndromes: Clinical and prognostic implications. J. Thorac. Cardiovasc. Surg. 2018, 156, 1776–1785.e6. [Google Scholar] [CrossRef]
- Fujiyoshi, T.; Obikane, H.; Nagao, T.; Ogino, H. Relationship between the aortic root Z-score and degree of translamellar mucoid extracellular matrix accumulation. Surg. Today. 2022, 52, 408–413. [Google Scholar] [CrossRef]
- Malaisrie, S.C.; Szeto, W.Y.; Halas, M.; Girardi, L.N.; Coselli, J.S.; Sundt, T.M.; Chen, E.P.; Fischbein, M.P.; Gleason, T.G.; Okita, Y.; et al. The American Association for Thoracic Surgery expert consensus document: Surgical treatment of acute type A aortic dissection. J. Thorac. Cardiovasc. Surg. 2021, 162, 735–758.e2. [Google Scholar] [CrossRef]
- Farag, M.; Büsch, C.; Rylski, B.; Pöling, J.; Dohle, D.S.; Sarvanakis, K.; Hagl, C.; Krüger, T.; Detter, C.; Holubec, T.; et al. Early outcomes of patients with Marfan syndrome and acute aortic type A dissection. J. Thorac. Cardiovasc. Surg. 2021, 166, 25–34.e8. [Google Scholar] [CrossRef]
- Pisano, C.; Balistreri, C.R.; Nardi, P.; Altieri, C.; Bertoldo, F.; Buioni, D.; Ferrante, M.S.; Asta, L.; Trombetti, D.; Ruvolo, G. Risk of aortic dissection in patients with ascending aorta aneurysm: A new biological, morphological, and biomechanical network behind the aortic diameter. Vessel. Plus. 2020, 4, 33. [Google Scholar] [CrossRef]
- Haverich, A.; Boyle, E.C. Aortic dissection is a disease of the vasa vasorum. JTCVS Open 2021, 5, 30–32. [Google Scholar] [CrossRef] [PubMed]
- Calafiore, A.M.; Katsavrias, K.; Di Marco, M.; Guarracini, S.; Di Mauro, M. Commentary: Vasa vasorum dysfunction and acute aortic syndromes: When guidelines do not follow the evolution of knowledge. JTCVS Open 2021, 5, 33–34. [Google Scholar] [CrossRef] [PubMed]
- Amemiya, K.; Mousseaux, E.; Ishibashi-Ueda, H.; Achouh, P.; Ochiai, M.; Bruneval, P. Impact of histopathological changes in ascending aortic diseases. Int. J. Cardiol. 2020, 311, 91–96. [Google Scholar] [CrossRef] [PubMed]
- De Martino, A.; Ballestracci, P.; Faggioni, L.; Pratali, S.; Morganti, R.; Pucci, A.; Bortolotti, U. Incidence of Aortitis in Surgical Specimens of the Ascending Aorta Clinical Implications at Follow-Up. Semin. Thorac. Cardiovasc. Surg. 2019, 31, 751–760. [Google Scholar] [CrossRef] [PubMed]
- Juraszek, A.; Czerny, M.; Rylski, B. Update in aortic dissection. Trends. Cardiovasc. Med. 2021, 32, 456–461. [Google Scholar] [CrossRef]
- Mehta, C.K.; Son, A.Y.; Chia, M.C.; Budd, A.N.; Allen, B.D.; Vassallo, P.; Hoel, A.W.; Brady, W.J.; Nable, J.V. Management of acute aortic syndromes from initial presentation to definitive treatment. Am. J. Emerg. Med. 2022, 51, 108–113. [Google Scholar] [CrossRef]
- Yuan, X.; Clough, R.E.; Nienaber, C.A. Acute aortic syndrome. Medicine 2022, 50, 449–452. [Google Scholar] [CrossRef]
- Bonaca, M.P.; Morrow, D.A. New clues for optimal diagnosis and treatment of an old foe: The acute aortic syndrome. Eur. Heart. J. Acute. Cardiovasc. Care. 2020, 9, S1–S2. [Google Scholar] [CrossRef]
- Pupovac, S.S.; Hemli, J.M.; Bavaria, J.E.; Patel, H.J.; Trimarchi, S.; Pacini, D.; Bekeredjian, R.; Chen, E.P.; Myrmel, T.; Ouzounian, M.; et al. Moderate Versus Deep Hypothermia in Type A Acute Aortic Dissection Repair: Insights from the International Registry of Acute Aortic Dissection. Ann. Thorac. Surg. 2021, 112, 1893–1899. [Google Scholar] [CrossRef]
- Freundt, M.; Kolat, P.; Friedrich, C.; Salem, M.; Gruenewald, M.; Elke, G.; Pühler, T.; Cremer, J.; Haneya, A. Preoperative Predictors of Adverse Clinical Outcome in Emergent Repair of Acute Type A Aortic Dissection in 15 Year Follow Up. J. Clin. Med. 2021, 10, 5370. [Google Scholar] [CrossRef]
- Vagnarelli, F.; Corsini, A.; Lorenzini, M.; Pacini, D.; Ferlito, M.; Reggiani, M.L.B.; Longhi, S.; Nanni, S.; Norscini, G.; Cinti, L.; et al. Acute heart failure in patients with acute aortic syndrome: Pathophysiology and clinical-prognostic implications. Eur. J. Heart. Fail. 2015, 17, 917–924. [Google Scholar] [CrossRef] [PubMed]
- Milewicz, D.M.; Guo, D.; Hostetler, E.; Marin, I.; Pinard, A.C.; Cecchi, A.C. Update on the genetic risk for thoracic aortic aneurysms and acute aortic dissections: Implications for clinical care. J. Cardiovasc. Surg. 2021, 62, 203–210. [Google Scholar] [CrossRef] [PubMed]
- Bossone, E.; Gorla, R.; Ranieri, B.; Russo, V.; Jakob, H.; Erbel, R. Initiating a New Era of Cardiovascular Diagnosis and Therapy in Acute Aortic Syndromes: The Mainz-Essen Experience (Part I)-Imaging and Biomarkers. Aorta 2021, 9, 127–138. [Google Scholar] [CrossRef] [PubMed]
- Yamamoto, T.; Endo, D.; Shimada, A.; Matsushita, S.; Asai, T.; Amano, A. Surgical treatment of acute aortic dissection in a patient with SLE and prior antiphospholipid syndrome on therapy for over 30 years: A case report. BMC Cardiovasc. Disord. 2022, 22, 216. [Google Scholar] [CrossRef]
- Guimbretière, G.; Nusinovici, S.; Monnot, A.; Sobocinski, J.; Sénage, T.; Delsart, P.; Gourraud, P.-A.; Maurel, B. Impact of Relative Change in Temperature and Atmospheric Pressure on Acute Aortic Syndrome Occurrence in France. Sci. Rep. 2020, 10, 76. [Google Scholar] [CrossRef]
- Huckaby, L.V.; Sultan, I.; Trimarchi, S.; Leshnower, B.; Chen, E.P.; Brinster, D.R.; Myrmel, T.; Estrera, A.L.; Montgomery, D.G.; Korach, A.; et al. Sex-Based Aortic Dissection Outcomes From the International Registry of Acute Aortic Dissection. Ann. Thorac. Surg. 2022, 113, 498–505. [Google Scholar] [CrossRef]
Figure 1.
Stepwise approach used in the study.
Figure 2.
Representation of overall mortality.
Figure 3.
Aortic wall with severe medial degeneration. The multifocal MEMA breaks across the lamellar units (A), disrupting the continuity of elastic fibers and expanding into the adjacent units (B). The elastic lamellae are completely destroyed (C), and the architectural distortion is enhanced by fibrosis (D).
Figure 3.
Aortic wall with severe medial degeneration. The multifocal MEMA breaks across the lamellar units (A), disrupting the continuity of elastic fibers and expanding into the adjacent units (B). The elastic lamellae are completely destroyed (C), and the architectural distortion is enhanced by fibrosis (D).
Figure 4.
Aortic wall with moderate medial degeneration. The normal architecture of the aortic wall is effaced due to matrix accumulation (A,B), which leads to fragmentation of the elastic fibers in some areas where MEMA is more pronounced (C). The proliferation of collagen fibers is more evident than the fibrosis encountered in mild medial degeneration (D).
Figure 4.
Aortic wall with moderate medial degeneration. The normal architecture of the aortic wall is effaced due to matrix accumulation (A,B), which leads to fragmentation of the elastic fibers in some areas where MEMA is more pronounced (C). The proliferation of collagen fibers is more evident than the fibrosis encountered in mild medial degeneration (D).
Figure 5.
Aortic wall with mild medial degeneration: longitudinal sections. The mucoid accumulation causes the expansion of the intralamellar space, visible on HE (A) and PAS Alcian staining (B). MEMA compresses the elastic fibers surrounding the lamellar units, which appear thinner and collapsed (C). Focal fibrotic areas can be observed on the trichrome stain (D).
Figure 5.
Aortic wall with mild medial degeneration: longitudinal sections. The mucoid accumulation causes the expansion of the intralamellar space, visible on HE (A) and PAS Alcian staining (B). MEMA compresses the elastic fibers surrounding the lamellar units, which appear thinner and collapsed (C). Focal fibrotic areas can be observed on the trichrome stain (D).
Figure 6.
The link between histopathological score and mortality rate.
Table 1.
Clinical characteristics of patients with aortic dissection and aortic aneurysm.
| Parameter | Aortic Dissection (n = 52) | Aortic Aneurysm (n = 56) | OR | p-Value |
|---|---|---|---|---|
| Male | 36 (69.23%) | 42 (75%) | 0.8654 | 0.5266 |
| Female | 16 (30.77%) | 14 (25%) | ||
| Age (mean ± SD) (median) | 62.42 ± 12.79 | 57.20 ± 9.572 | - | 0.0072 |
| Hospitalization days (mean ± SD) | 8.769 ± 7.722 | 11.11 ± 11.20 | - | 0.1631 |
Table 2.
The rate of complications in patients with aortic dissection and aortic aneurysm.
| Parameter | Aortic Dissection (n = 52) | Aortic Aneurysm (n = 56) | OR | p-Value |
|---|---|---|---|---|
| Preoperative | ||||
| Pericardial effusion | 21 (40.38%) | 0 (0.00%) | 77.127 | <0.0001 |
| Cardiac tamponade | 10 (19.23%) | 0 (0.00%) | 27.918 | 0.0004 |
| Malperfusion syndrome | 2 (3.85%) | 0 (0.00%) | 5.594 | 0.2295 |
| Pleural effusion | 0 (0.00%) | 1 (1.79%) | 2.3186 | 0.9999 |
| Acute kidney injury | 6 (11.54%) | 7 (12.50%) | 0.9532 | 0.9999 |
| Chronic kidney diseases | 1 (1.92%) | 2 (3.57%) | 0.6863 | 0.9999 |
| Stroke | 1 (1.92%) | 0 (0.00%) | 2.098 | 0.4815 |
| Syncope | 2 (3.85%) | 0 (0.00%) | 5.594 | 0.2295 |
| Systemic hypertension | 32 (61.54%) | 18 (32.14%) | 3.378 | 0.0036 |
| Bicuspid aortic valve | 17 (30.36%) | 3 (5.77%) | 7.120 | 0.0011 |
| Aortic valve regurgitation | 32 (61.54%) | 27 (48.21%) | 1.1719 | 0.1809 |
| Aortic valve stenosis | 2 (3.85%) | 7 (12.50%) | 0.2800 | 0.1638 |
| Atrial fibrillation | 28 (50.00%) | 7 (13.46%) | 6.429 | <0.0001 |
| Postoperative | ||||
| Days in the ICU (mean ± SD) | 2.750 ± 2.317 | 4.268 ± 5.786 | - | 0.6173 |
| Intubation time-hours (mean ± SD) | 36.63 ± 51.31 | 65.90 ± 130.4 | - | 0.2969 |
| Hepatic dysfunction | 18 (34.62%) | 23 (41.07%) | 0.7596 | 0.5541 |
| Renal dysfunction | 11 (21.15%) | 15 (26.79%) | 0.7333 | 0.5100 |
| Hemofiltration | 7 (13.46%) | 11 (19.64%) | 0.6364 | 0.4461 |
| Systemic infection | 2 (3.85%) | 4 (7.14%) | 0.5200 | 0.6799 |
| Reintervention | 10 (19.23%) | 7 (12.50%) | 1.667 | 0.4304 |
Table 3.
Microscopic scores in aortic dissection vs. aortic aneurysm samples.
| Histological Medial Degenerative Change | Degenerative Degree | Aortic Dissection (n = 52) | Aortic Aneurysm (n = 56) | p-Value |
|---|---|---|---|---|
| Interlamellar (MEMA-i) | Mild | 0 (0.00%) | 6 (10.71%) | <0.0001 |
| Moderate | 9 (17.31%) | 24 (42.86%) | ||
| Severe | 43 (82.69%) | 26 (46.43%) | ||
| Translamellar (MEMA-t) | Mild | 4 (7.69%) | 20 (40.00%) | 0.0001 |
| Moderate | 40 (79.62%) | 24 (48.00%) | ||
| Severe | 8 (15.38%) | 6 (12.00%) | ||
| Elastic fragmentation or loss | Mild | 11 (21.15%) | 29 (54.72%) | 0.0011 |
| Moderate | 37 (71.15%) | 20 (37.74%) | ||
| Severe | 4 (7.69%) | 4 (7.55%) | ||
| Smooth muscle cell nuclei loss | Mild | 26 (50.98%) | 26 (70.27%) | <0.0001 |
| Moderate | 23 (45.10%) | 10 (27.03%) | ||
| Severe | 2 (3.92%) | 1 (2.70%) | ||
| Laminar medial collapse | Mild | 22 (45.83%) | 24 (60.00%) | 0.0223 |
| Moderate | 22 (45.83%) | 14 (35.00%) | ||
| Severe | 4 (8.33%) | 2 (5.00%) |
Table 4.
Subdivision of the microscopic score in aortic dissection vs. aortic aneurysm.
| Histological Medial Degenerative Change | Degenerative Degree | Subdivision | Aortic Dissection (n = 52) | Aortic Aneurysm (n = 56) | p-Value |
|---|---|---|---|---|---|
| Interlamellar (MEMA-i) | Mild | Multifocal | 0 (0.00%) | 4 (100%) | 0.2378 |
| Focal | 0 (0.00%) | 2 (100%) | |||
| Moderate | Multifocal | 9 (30.00%) | 21 (70.00%) | 0.5447 | |
| Focal | 0 (0.00%) | 3 (100%) | |||
| Severe | Multifocal | 40 (60.61%) | 26 (39.39%) | 0.2852 | |
| Focal | 3 (100%) | 0 (0.00%) | |||
| Translamellar (MEMA-t) | Mild | Multifocal | 3 (23.08%) | 10 (76.92%) | 0.5963 |
| Focal | 1 (9.09%) | 10 (90.91%) | |||
| Moderate | Multifocal | 29 (69.05%) | 13 (30.95%) | 0.1768 | |
| Focal | 11 (50.00%) | 11 (50.00%) | |||
| Severe | Multifocal | 4 (44.44%) | 5 (55.56%) | 0.3007 | |
| Focal | 4 (80.00%) | 1 (20.00%) | |||
| Elastic fragmentation or loss | Mild | Multifocal | 5 (31.32%) | 11 (68.57%) | 0.7275 |
| Focal | 6 (25.00%) | 18 (75.00%) | |||
| Moderate | Multifocal | 22 (61.11%) | 14 (38.89%) | 0.5675 | |
| Focal | 15 (71.43%) | 6 (28.57%) | |||
| Severe | Multifocal | 1 (20.00%) | 4 (80.00%) | 0.1429 | |
| Focal | 3 (100%) | 0 (0.00%) | |||
| Smooth muscle cell nuclei loss | Mild | Multifocal | 12 (50.00%) | 12 (50.00%) | 0.9999 |
| Focal | 14 (50.00%) | 14 (50.00%) | |||
| Moderate | Multifocal | 12 (63.16%) | 7 (36.84%) | 0.4551 | |
| Focal | 11 (78.57%) | 3 (21.43%) | |||
| Severe | Multifocal | 2 (100%) | 0 (0.00%) | - | |
| Focal | 0 (0.00%) | 1 (100%) | |||
| Laminar medial collapse | Mild | Multifocal | 14 (73.68%) | 5 (26.32%) | 0.0063 |
| Focal | 8(29.63%) | 19(70.37%) | |||
| Moderate | Multifocal | 13 (61.90%) | 8 (38.10%) | 0.9999 | |
| Focal | 9 (60.00%) | 6 (40.00%) | |||
| Severe | Multifocal | 2 (100%) | 0 (0.00%) | 0.4667 | |
| Focal | 2 (50.00%) | 2 (50.00%) |
Table 5.
Overall medial degeneration in aortic dissection vs. aortic aneurysm.
| Severity | Aortic Dissection | Aortic Aneurysm | p-Value |
|---|---|---|---|
| Mild (n = 26) | 2 (7.69%) | 24 (92.31%) | <0.0001 |
| Moderate (n = 64) | 39 (60.94%) | 25 (39.06%) | |
| Severe (n = 18) | 11 (61.11%) | 7 (38.89%) |
Table 6.
Analysis of mortality in relation to histopathological score.
| In-Hospital Mortality | |||||
|---|---|---|---|---|---|
| Predictors | B | Exp(B) | 95% CI for EXP(B) | p-value | |
| Lower | Upper | ||||
| Histopathologic score | 1.123 | 3.073 | 1.467 | 6.439 | 0.0029 |
| Overall Mortality | |||||
| Predictors | B | Exp(B) | 95% CI for EXP(B) | p-value | |
| Lower | Upper | ||||
| Histopathologic score | 1.065 | 2.900 | 1.455 | 5.779 | 0.0025 |
Table 7.
Assessment criteria used for the scoring of aortic medial degeneration.
| Mucoid Extracellular Matrix Accumulation, Intralamellar (MEMA-i) | Mucoid Extracellular Matrix Accumulation, Translamellar (MEMA-t) | Elastic Fiber Fragmentation and Loss | Loss of Smooth Muscle Cell Nuclei | Laminar Medial Collapse | Overall Medial Degeneration | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Absent | Absent | Absent | Absent | Absent | ABSENT (score 0) | |||||
| Mild | Mild | Mild | Mild | Mild | MILD (score 1) | |||||
| Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | |
| Moderate | Moderate | Moderate | Moderate | Moderate | MODERATE (score 2) | |||||
| Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | |
| Severe | Severe | Severe | Severe | Severe | SEVERE (score 3) | |||||
| Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | Focal | Multifocal | |
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MDPI and ACS Style
Banceu, C.M.; Gurzu, S.; Satala, C.-B.; Ghiga, D.; Neamtu, M.H.; Voth, V.; Liebrich, M.; Suciu, H. Histopathological Gap in Aortic Diseases: A Prospective Analysis. Int. J. Mol. Sci. 2023, 24, 15470. https://doi.org/10.3390/ijms242015470
AMA Style
Banceu CM, Gurzu S, Satala C-B, Ghiga D, Neamtu MH, Voth V, Liebrich M, Suciu H. Histopathological Gap in Aortic Diseases: A Prospective Analysis. International Journal of Molecular Sciences. 2023; 24(20):15470. https://doi.org/10.3390/ijms242015470
Chicago/Turabian StyleBanceu, Cosmin Marian, Simona Gurzu, Catalin-Bogdan Satala, Dana Ghiga, Mihai Halic Neamtu, Vladimir Voth, Markus Liebrich, and Horatiu Suciu. 2023. "Histopathological Gap in Aortic Diseases: A Prospective Analysis" International Journal of Molecular Sciences 24, no. 20: 15470. https://doi.org/10.3390/ijms242015470
APA StyleBanceu, C. M., Gurzu, S., Satala, C. -B., Ghiga, D., Neamtu, M. H., Voth, V., Liebrich, M., & Suciu, H. (2023). Histopathological Gap in Aortic Diseases: A Prospective Analysis. International Journal of Molecular Sciences, 24(20), 15470. https://doi.org/10.3390/ijms242015470
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