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Nutrition and Pediatric Gastroenterology

A special issue of Nutrients (ISSN 2072-6643). This special issue belongs to the section "Clinical Nutrition".

Deadline for manuscript submissions: closed (30 June 2020) | Viewed by 111007

Special Issue Editor


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Guest Editor
Pediatric Gastroenterology and Cystic Fibrosis Unit, Department of Human Pathology and Pediatrics, University of Messina, Via Consolare Valeria, 98124 Messina, Italy
Interests: pediatric gastroenterology; digestive endoscopy; pediatric nutrition; enteral nutrition; artificial nutrition; inflammatory bowel disease; functional gastrointestinal disease; feeding disorders

Special Issue Information

Dear Colleagues,

Nutrition and intestinal function are strictly interrelated. The main role of the gut is to digest and absorb nutrients in order to maintain life. Consequently, chronic gastrointestinal disease commonly results in malnutrition and increased morbidity and mortality. On the other hand, chronic malnutrition impairs digestive and absorptive function because food and nutrients are not only the major trophic factors to the gut but also contribute to the structure and functioning of digestive enzymes and absorptive cells. Finally, specific nutrients can induce or prevent gastrointestinal disease (for example, gluten-sensitive enteropathy, or the role of dietary antigens and elemental diets in inducing remission in patients with Crohn’s disease). In conclusion, nutrition has both a supportive and therapeutic role in the management of many gastrointestinal diseases. All these aspects get high relevance during infancy and childhood, dynamic phases of life characterized by rapid growth, development and developmental plasticity, in which a sufficient amount and appropriate composition of substrates both in health and disease are crucial for growth, functional outcomes, and long-term health. On this topic, you are invited to submit proposals for manuscripts that fit the objectives and topics of this Special Issue. The objective of this proposed Special Issue on “Nutrition and Pediatric Gastroenterology” is to publish selected papers (reviews and/or clinical or experimental studies) detailing specific aspects of nutrition that could play a role in pediatric gastrointestinal disease, both functional and nonfunctional.

Prof. Dr. Claudio Romano
Guest Editor

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Keywords

  • Nutrition
  • Gastrointestinal disease
  • Malnutrition
  • Pediatrics
  • Feeding disorder
  • Functional gastrointestinal disorders
  • Enteral nutrition
  • Parenteral nutrition

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Published Papers (9 papers)

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Editorial

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3 pages, 173 KiB  
Editorial
Nutrition in Pediatric Gastroenterology
by Claudio Romano and Valeria Dipasquale
Nutrients 2021, 13(6), 1965; https://doi.org/10.3390/nu13061965 - 8 Jun 2021
Cited by 1 | Viewed by 2685
Abstract
Nutrition and intestinal function are strictly interrelated [...] Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)

Research

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12 pages, 1044 KiB  
Article
Lactobacillus reuteri DSM 17938 and Agave Inulin in Children with Cerebral Palsy and Chronic Constipation: A Double-Blind Randomized Placebo Controlled Clinical Trial
by Andrea A. García Contreras, Edgar M. Vásquez Garibay, Carmen A. Sánchez Ramírez, Mary Fafutis Morris and Vidal Delgado Rizo
Nutrients 2020, 12(10), 2971; https://doi.org/10.3390/nu12102971 - 28 Sep 2020
Cited by 23 | Viewed by 5951
Abstract
The main objective was to assess the efficacy of a probiotic (Lactobacillus reuteri DSM 17938), a prebiotic (agave inulin), and a synbiotic on the stool characteristics in children with cerebral palsy and chronic constipation. Thirty-seven children with cerebral palsy and chronic constipation [...] Read more.
The main objective was to assess the efficacy of a probiotic (Lactobacillus reuteri DSM 17938), a prebiotic (agave inulin), and a synbiotic on the stool characteristics in children with cerebral palsy and chronic constipation. Thirty-seven children with cerebral palsy and chronic constipation were included. The probiotic group received 1 × 108 colony forming unit (cfu) of L. reuteri DSM 17938 plus placebo, the prebiotic group received 4 g of agave inulin plus placebo, the synbiotic group received L. reuteri DSM 17938 plus agave inulin, and the placebo group received two placebos for 28 days. The probiotic group showed a significant decrease in stool pH (p = 0.014). Stool consistency improved in the prebiotic group (p = 0.008). The probiotic, prebiotic, and synbiotic groups showed a significant improvement in the history of excessive stool retention, the presence of fecal mass in the rectum, and the history of painful defecation. L. reuteri concentration in feces was higher in the probiotic group than in the placebo group (p = 0.001) and showed an inverse correlation with stool pH in the probiotic group (r = −0.762, p = 0.028). This study showed that the use of L. reuteri DSM 17938 and/or agave inulin improved the stool characteristics such as the history of painful defecation and the presence of fecal mass in the rectum against placebo in children with cerebral palsy and chronic constipation. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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10 pages, 1496 KiB  
Article
The Gluten Free Diet’s Impact on Growth in Children with Celiac Disease in Two Different Countries
by Naire Sansotta, Stefano Guandalini, Simone Romano, Karine Amirikian, Marco Cipolli, Gloria Tridello, Silvia Barzaghi and Hilary Jericho
Nutrients 2020, 12(6), 1547; https://doi.org/10.3390/nu12061547 - 26 May 2020
Cited by 12 | Viewed by 3917
Abstract
The effects of gluten free diet (GFD) on body mass index (BMI) and growth parameters in pediatric patients with celiac disease (CD) and their dependence on different socio-cultural environments are poorly known. We conducted an international retrospective study on celiac patients diagnosed at [...] Read more.
The effects of gluten free diet (GFD) on body mass index (BMI) and growth parameters in pediatric patients with celiac disease (CD) and their dependence on different socio-cultural environments are poorly known. We conducted an international retrospective study on celiac patients diagnosed at the University of Verona, Italy, and at the University of Chicago, Chicago, IL, USA, as underweight. A total of 140 celiac children and 140 controls (mean age 8.4 years) were enrolled in Chicago; 125 celiac children and 125 controls (mean age 7.3 years, NS) in Verona. At time of diagnosis, Italian celiac children had a weight slightly lower (p = 0.060) and a BMI z-score significantly (p < 0.001) lower than their American counterparts. On GFD, Italian celiac children showed an increased prevalence of both underweight (19%) as well as overweight (9%), while American children showed a decrease prevalence of overweight/obese. We concluded that while the GFD had a similar impact on growth of celiac children in both countries, the BMI z-score rose more in American than in Italian celiac children. Additionally, in Italy, there was an alarming increase in the proportion of celiac children becoming underweight. We speculate that lifestyle and cultural differences may explain the observed variations. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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6 pages, 554 KiB  
Article
The Cow’s Milk-Related Symptom Score (CoMiSSTM): Health Care Professional and Parent and Day-to-Day Variability
by Yvan Vandenplas, Eva Carvajal, Stefaan Peeters, Nadine Balduck, Yesra Jaddioui, Carmen Ribes-Koninckx and Koen Huysentruyt
Nutrients 2020, 12(2), 438; https://doi.org/10.3390/nu12020438 - 9 Feb 2020
Cited by 16 | Viewed by 3049
Abstract
The Cow’s Milk-related Symptom Score (CoMiSSTM) was created as an awareness tool for cow’s milk allergy. The aim of the present study was to analyze the inter-rater variability between a pediatrician, parents, and day to day variability. A Health Care Professional [...] Read more.
The Cow’s Milk-related Symptom Score (CoMiSSTM) was created as an awareness tool for cow’s milk allergy. The aim of the present study was to analyze the inter-rater variability between a pediatrician, parents, and day to day variability. A Health Care Professional (HCP) and parent filled in the CoMiSS independently and blinded for each other to evaluate inter-rater variability. In order to validate day-to-day variability, a parent filled in the CoMiSS during 3 consecutive days and was compared to the CoMiSS scored by the HCP. The absolute agreement between parent and HCP was 75%, and 92.6% and 100% with a tolerance of 0, 1, and 2 points, respectively, resulting in excellent agreement with an intraclass correlation coefficient (ICC) 0.981 (95% Confidence Interval 0.974–0.986, p < 0.001). Day-to-day variability during 3 consecutive days resulted in an absolute agreement of 30%, increasing to 80% and 88.6% when 2 and 3 points, respectively, were accepted. The ICC was excellent for the parental prospective scores (0.93, 95% CI 0.90–0.96; p < 0.001). Day-to-day variability indicates that CoMiSS has a moderate inter-rater reliability. A very low variability was observed when scored prospectively over three days. Data suggest that the CoMiSS can reliably be scored by parents without additional training. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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Review

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19 pages, 1324 KiB  
Review
Diet and Nutrients in Gastrointestinal Chronic Diseases
by Antonio Corsello, Daniela Pugliese, Antonio Gasbarrini and Alessandro Armuzzi
Nutrients 2020, 12(9), 2693; https://doi.org/10.3390/nu12092693 - 3 Sep 2020
Cited by 43 | Viewed by 13160
Abstract
Diet and nutrition are known to play key roles in many chronic gastrointestinal diseases, regarding both pathogenesis and therapeutic possibilities. A strong correlation between symptomatology, disease activity and eating habits has been observed in many common diseases, both organic and functional, such as [...] Read more.
Diet and nutrition are known to play key roles in many chronic gastrointestinal diseases, regarding both pathogenesis and therapeutic possibilities. A strong correlation between symptomatology, disease activity and eating habits has been observed in many common diseases, both organic and functional, such as inflammatory bowel disease and irritable bowel syndrome. New different dietary approaches have been evaluated in order improve patients’ symptoms, modulating the type of sugars ingested, the daily amount of fats or the kind of metabolites produced in gut. Even if many clinical studies have been conducted to fully understand the impact of nutrition on the progression of disease, more studies are needed to test the most promising approaches for different diseases, in order to define useful guidelines for patients. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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9 pages, 235 KiB  
Review
Acute Malnutrition in Children: Pathophysiology, Clinical Effects and Treatment
by Valeria Dipasquale, Ugo Cucinotta and Claudio Romano
Nutrients 2020, 12(8), 2413; https://doi.org/10.3390/nu12082413 - 12 Aug 2020
Cited by 85 | Viewed by 37840
Abstract
Acute malnutrition is a nutritional deficiency resulting from either inadequate energy or protein intake. Children with primary acute malnutrition are common in developing countries as a result of inadequate food supply caused by social, economic, and environmental factors. Secondary acute malnutrition is usually [...] Read more.
Acute malnutrition is a nutritional deficiency resulting from either inadequate energy or protein intake. Children with primary acute malnutrition are common in developing countries as a result of inadequate food supply caused by social, economic, and environmental factors. Secondary acute malnutrition is usually due to an underlying disease causing abnormal nutrient loss, increased energy expenditure, or decreased food intake. Acute malnutrition leads to biochemical changes based on metabolic, hormonal, and glucoregulatory mechanisms. Most children with primary acute malnutrition can be managed at home with nutrition-specific interventions (i.e., counseling of parents, ensuring household food security, etc.). In case of severe acute malnutrition and complications, inpatient treatment is recommended. Secondary acute malnutrition should be managed by treating the underlying cause. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
16 pages, 537 KiB  
Review
Failure to Thrive in the Outpatient Clinic: A New Insight
by Antonella Lezo, Letizia Baldini and Monica Asteggiano
Nutrients 2020, 12(8), 2202; https://doi.org/10.3390/nu12082202 - 24 Jul 2020
Cited by 15 | Viewed by 10472
Abstract
Failure to thrive (FTT) is an abnormal growth pattern determined by inadequate nutrition. It is a common problem in children, representing 5% to 10% of patients seen in an outpatient setting. Many definitions have been proposed based on anthropometric deterioration; however, they show [...] Read more.
Failure to thrive (FTT) is an abnormal growth pattern determined by inadequate nutrition. It is a common problem in children, representing 5% to 10% of patients seen in an outpatient setting. Many definitions have been proposed based on anthropometric deterioration; however, they show poor concordance. No single definition is sufficiently sensitive in identifying faltering growth whilst a combination of multiple criteria seems more accurate. In light of the recent redefinition of pediatric malnutrition as a disequilibrium between requirements and intakes of energy, and macro- and micronutrients, a wider conception of FTT as an unsatisfactory nutritional status related to poor growth and health is useful. Although the most severe problems of micronutrient malnutrition are found in developing countries, people of all regions of the world can be affected by micronutrient deficiencies (MNDs), a form of undernutrition with relevant effects on growth and health. Changes in diets and lifestyle, elimination diets, food insecurity, and food intake disorders create the conditions at risk of faltering growth and MNDs. This new insight integrates the “classical” anthropometric criteria for definition and treatment, in the aim of warranting both a regular increase in size and an overall adequate development and health status. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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19 pages, 1420 KiB  
Review
Persistent Iron Deficiency Anemia in Patients with Celiac Disease Despite a Gluten-Free Diet
by Gianpiero Stefanelli, Angelo Viscido, Salvatore Longo, Marco Magistroni and Giovanni Latella
Nutrients 2020, 12(8), 2176; https://doi.org/10.3390/nu12082176 - 22 Jul 2020
Cited by 36 | Viewed by 13483
Abstract
Celiac disease (CD) is an autoimmune disorder characterized by intolerance to dietary gluten in genetically predisposed subjects. Iron deficiency anemia (IDA) is a common sign in CD, being the only abnormality in approximately 40% of celiac patients. A multifactorial etiology leads to IDA [...] Read more.
Celiac disease (CD) is an autoimmune disorder characterized by intolerance to dietary gluten in genetically predisposed subjects. Iron deficiency anemia (IDA) is a common sign in CD, being the only abnormality in approximately 40% of celiac patients. A multifactorial etiology leads to IDA in CD. The two main causes are the villous atrophy of the mucosa at the site of iron absorption (the duodenum) and the resulting inflammation, which triggers the mechanism that leads to the anemia of chronic disease. Until now, it has been unclear why some patients with CD continue to have IDA despite a careful gluten-free diet (GFD) and the normalization of villous atrophy. Furthermore, some celiac patients are refractory to oral iron supplementation despite the healing of the mucosa, and they thus require periodic intravenous iron administration. The Marsh classification evaluates the degree of inflammation and villous atrophy, but it does not assess the possible persistence of ultrastructural and molecular alterations in enterocytes. The latter was found in CD in remission after adopting a GFD and could be responsible for the persistently reduced absorption of iron and IDA. Even in non-celiac gluten sensitivity, anemia is present in 18.5–22% of patients and appears to be related to ultrastructural and molecular alterations in intestinal microvilli. It is possible that a genetic component may also play a role in IDA. In this review, we evaluate and discuss the main mechanisms of IDA in CD and the possible causes of its persistence after adopting a GFD, as well as their therapeutic implications. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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29 pages, 1962 KiB  
Review
Non-IgE-Mediated Gastrointestinal Food Allergies in Children: An Update
by Roxane Labrosse, François Graham and Jean-Christoph Caubet
Nutrients 2020, 12(7), 2086; https://doi.org/10.3390/nu12072086 - 14 Jul 2020
Cited by 90 | Viewed by 19214
Abstract
Non-immunoglobulin E-mediated gastrointestinal food allergic disorders (non-IgE-GI-FA) include food protein-induced enterocolitis syndrome (FPIES), food protein-induced enteropathy (FPE) and food protein-induced allergic proctocolitis (FPIAP), which present with symptoms of variable severity, affecting the gastrointestinal tract in response to specific dietary antigens. The diagnosis of [...] Read more.
Non-immunoglobulin E-mediated gastrointestinal food allergic disorders (non-IgE-GI-FA) include food protein-induced enterocolitis syndrome (FPIES), food protein-induced enteropathy (FPE) and food protein-induced allergic proctocolitis (FPIAP), which present with symptoms of variable severity, affecting the gastrointestinal tract in response to specific dietary antigens. The diagnosis of non-IgE-GI-FA is made clinically, and relies on a constellation of typical symptoms that improve upon removal of the culprit food. When possible, food reintroduction should be attempted, with the documentation of symptoms relapse to establish a conclusive diagnosis. Management includes dietary avoidance, nutritional counselling, and supportive measures in the case of accidental exposure. The prognosis is generally favorable, with the majority of cases resolved before school age. Serial follow-up to establish whether the acquisition of tolerance has occurred is therefore essential in order to avoid unnecessary food restriction and potential consequent nutritional deficiencies. The purpose of this review is to delineate the distinctive clinical features of non-IgE-mediated food allergies presenting with gastrointestinal symptomatology, to summarize our current understanding of the pathogenesis driving these diseases, to discuss recent findings, and to address currents gaps in the knowledge, to guide future management opportunities. Full article
(This article belongs to the Special Issue Nutrition and Pediatric Gastroenterology)
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