Evidence map›Paper›PMID 41429819›Full record

ArticleScientific reports2025

Gut microbiota analysis in children with autism spectrum disorder and their family members.

Qun Chen, Jing Xu, Jingjing Yang, Xiaoya Qin, Jiajun Fan, Hailin Ke, Ziyue Yang, Wenjie Zheng, Xingyu Li, Lihong Huang and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

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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

11 authors.

Qun Chen *Institute of Clinical Medical Research, The First Affiliated Hospital, School of Medicine, Xiamen University, Xiamen, 361003, Fujian, China.
Jing Xu *Department of Pediatrics, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Jingjing Yang *Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, 361003, Fujian, China.
Xiaoya QinNational Innovation Center for Advanced Medical Devices, Shenzhen, China.
Jiajun FanSiebel School of Computing and Data Science, University of Illinois Urbana-Champaign, Champaign, USA.
Hailin KeDepartment of Pediatrics, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Ziyue YangDepartment of Pediatrics, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Wenjie ZhengDepartment of Information Center, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Xingyu LiInstitute of Clinical Medical Research, The First Affiliated Hospital, School of Medicine, Xiamen University, Xiamen, 361003, Fujian, China. xingyuli22@yeah.net.
Lihong HuangDepartment of Information Center, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China. lemonlh@xmu.edu.cn.
Wanshan NingInstitute of Clinical Medical Research, The First Affiliated Hospital, School of Medicine, Xiamen University, Xiamen, 361003, Fujian, China. ningwanshan@xmu.edu.cn.

Funding

Fujian Provincial Health Technology Project 2024GGB18National Key Research and Development Program of China 2022YFC2704300National Natural Science Foundation of China 32400532Project of Xiamen Cell Therapy Research Center, Xiamen, Fujian, China Grant No.3502Z20214001
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by deficits in social communication and interaction, alongside restricted, and repetitive behaviors. Emerging evidence suggests that gut microbiota alterations may contribute to ASD pathogenesis via the gut-brain axis. However, many previous studies have not adequately controlled for confounding genetic and environmental variables. In this study, we examined the gut microbiota profiles of 19 children with ASD, 8 siblings with non-ASD, and 36 parents from 17 families, providing a unique design that minimized biases related to shared genetic and familial environments. Metagenomic sequencing revealed significant differences in gut microbiota diversity and composition between groups. Specifically, children with ASD had lower abundances of Bifidobacterium and higher abundances of both Bacteroides and Clostridium species compared to their siblings, with notable dysbiosis correlated to ASD-specific symptoms. These findings highlight the potential role of microbiota alterations in ASD pathogenesis and suggest familial microbiota traits influenced by both genetic and environmental factors. Further exploration of gut microbial therapies could offer promising avenues for ASD intervention.

Indexed as

Autism Spectrum DisorderGastrointestinal MicrobiomeBacteroidesBifidobacteriumChildChild, PreschoolClostridiumDysbiosisFamilyFecesFemaleHumansMaleMetagenomicsSiblingsAutism spectrum disorderGut microbiotaMetagenomic sequencing

Identifiers

PMID41429819
PMCPMC12722752

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Registered trials

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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.