Butyrate Supplementation in Children With Autism Spectrum Disorder (ASD) and Functional Gastrointestinal Disorders
Effects of a Postbiotic Supplementation on Gastrointestinal and Core Symptoms in Autism Spectrum Disorder: A Multicenter Randomized Controlled Trial
Istituto Superiore di Sanità
128 participants
May 1, 2025
INTERVENTIONAL
Conditions
Summary
Autism spectrum disorder (ASD) is a neurodevelopmental condition occurring in 1:77 Italian children. Several comorbidities are reported, including functional gastrointestinal disorders (FGIDs) present in up to 70% of patients. FGIDs are disorders resulting from a combination of symptoms affecting motility, hypersensitivity, and other functions, which are not caused by anatomic or organic origin and that impact the severity of ASD core symptoms and complicate the clinical management of ASD children, especially those who are non-verbal. Evidence reports gut microbiome (GM) remodelling in ASD children, and postbiotic butyrate, a GM-derived metabolite, attenuates FGIDs in children and restores social behavior in ASD mouse models. Clinical data on butyrate effects in ASD are still scanty. The present study investigates the therapeutic effects of a 16-week oral postbiotic supplementation on clinical/behavioral profiles, gastrointestinal disturbances, gut microbiome, and immune and inflammatory biomarkers in peripheral blood and fecal samples in children with ASD and FGIDs. Using the Machine Learning (ML) approach, a subset of artificial intelligence, this study also aims to identify predictive factors implicated in the effect of the postbiotic supplementation on FGIDs, important for prevention through modulation of the microbiota. The investigators expect that treating FGIDs will have an impact on the behavioral and core symptoms of ASD and the quality of life of children and their families.
Eligibility
Inclusion Criteria3
- children aged 3-6 years
- both sexes
- ASD diagnosis and presence of FGIDs (6-item Gastrointestinal Severity Index (6-GSI) >7 from > 3 months)
Exclusion Criteria12
- age 6 years
- uncertain FGIDs diagnoses
- FGIDs symptoms duration <3 months
- concomitant presence of other chronic condition (adverse food reactions, metabolic disorders, infections)
- malformation and Gi or urinary tracts chronic diseases
- immunodeficiencies
- diabetes
- neurologic/cardiovascular/autoimmune diseases
- obesity
- malnutrition
- antibiotics and/or pre-/pro-/synbiotics use 6 months prior to enrollment
- last 12 months participation into other clinical trials
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Interventions
Daily supplementation with 1 sachet per day for 16 weeks
Daily supplementation with 1 sachet per day for 16 weeks
Locations(3)
View Full Details on ClinicalTrials.gov
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NCT06514573