Evidence map›Paper›PMID 42875511›Full record

ArticlePediatric research2026

Gut microbiota are linked to gastrointestinal symptoms and behavioral changes but not inflammation in autism spectrum disorder: a cross-sectional analysis.

Vaishali Harne, Nicole Y Fatheree, Angela V Serrano, Beanna Okeugo, Ana Fadhel Alvarez, Manouchehr Hessabi, Amirali Tahanan, Rosleen Mansour, Fernando Navarro, Essam Imseis and 12 more

Abstract read
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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Vaishali HarneDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Nicole Y FathereeDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Angela V SerranoTexas Children's Microbiome Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Beanna OkeugoDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Ana Fadhel AlvarezDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Manouchehr HessabiCenter for Clinical and Translational Science, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Amirali TahananCenter for Clinical and Translational Science, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Rosleen MansourLouis A. Faillace, MD, Department of Psychiatry and Behavioral Sciences, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Fernando NavarroDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Essam ImseisDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Supriya NairDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Wallace A GleasonDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Melissa R Van ArsdallDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Tu MaiDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Shabba A ArmbristerDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Salomea GiorgberidzeDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Mohammad H RahbarCenter for Clinical and Translational Science, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
MinJae LeeCenter for Clinical and Translational Science, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Deborah A PearsonLouis A. Faillace, MD, Department of Psychiatry and Behavioral Sciences, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
Ruth Ann LunaTexas Children's Microbiome Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Yuying LiuDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA.
J Marc RhoadsDivision of Gastroenterology, Department of Pediatrics, McGovern Medical School at UTHealth Houston, Houston, TX, USA. j.marc.rhoads@uth.tmc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastrointestinal (GI) symptoms are increased in children with autism spectrum disorder (ASD). We examined the relationship between ASD severity, intestinal inflammation, gut permeability, and dysbiosis.

methodsOur cross-sectional study examined baseline data from a clinical trial and included stools from typically developing (TD) controls and siblings. GI symptom severity was assessed using GI severity index (GSI) with Bristol stool scoring, while ASD symptoms were quantified using Social Responsiveness Scale (SRS-2). Biomarkers including plasma zonulin, occludin, and S100A9, and fecal calprotectin levels, were measured to assess intestinal permeability and inflammation. Fecal microbiota was analyzed using 16S rRNA sequencing.

resultsSeventy-two children with ASD were included for biomarker analysis, and 135 children's stools for microbiome analysis. A statistically significant correlation was observed between GSI and SRS-2 scores (p = 0.02). GSI and SRS-2 scores did not correlate with measured biomarkers, none of which were elevated above published normal values. Children with ASD had reduced fecal richness and distinct clustering of organisms, with increased relative abundance of Fusicatenibacter, Blautia, Sarcina, and Eubacterium, compared to TD children.

conclusionsChildren with ASD who had GI symptoms had increased Bacteroides and Ruminococci. Dysbiosis correlated with common GI symptoms, including flatulence, foul stools, and nighttime awakening. IMPACT: Children with ASD who have more disturbed social awareness are prone to more severe GI symptoms, reduced fecal microbial diversity and abnormal fecal microbial composition. Certain stool microbial taxa correlated with total GI symptom scores as well as with specific GI symptoms including flatulence, abdominal pain/irritability, and foul-smelling stools. However, we found no evidence of gastrointestinal or systemic inflammation, nor of increased gut permeability to explain the symptoms.

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.