Evidence map›Paper›PMID 42058178›Full record

Observational studyFrontiers in cellular and infection microbiology2026

Reduced gut microbial diversity characterized by decreased

Wei Tang, Qing Yang, Jiayu Ren, Xingyu Han, Cuifen Zhao

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in cellular and infection microbiology, 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

5 authors.

Wei TangDepartment of Pediatrics, Qilu Hospital of Shandong University, Jinan, China.
Qing YangDepartment of Pediatrics, Women's Hospital of Nanjing Medical University, Nanjing Women and Children's Healthcare Hospital, Nanjing, China.
Jiayu RenDepartment of Pediatrics, Qilu Hospital of Shandong University, Jinan, China.
Xingyu HanDepartment of Pediatrics, Qilu Hospital of Shandong University, Jinan, China.
Cuifen ZhaoDepartment of Pediatrics, Qilu Hospital of Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Vasovagal syncope (VVS) represents the most prevalent form of orthostatic intolerance in children and is characterized by recurrent fainting episodes that substantially impair quality of life and psychosomatic well-being. The pathogenesis of VVS is primarily associated with dysregulation of the autonomic nervous system. Emerging evidence suggests that the gut microbiota, a complex microbial community residing in the human intestine, plays a pivotal pathological role in various autonomic nervous system related disorders. However, data on the gut microbiota profile in pediatric VVS remain limited. The present study therefore aims to characterize gut microbiota changes in children with VVS and its subtypes, providing novel insights into the underlying mechanisms and potential therapeutic strategies. Method: Fecal samples were obtained from 40 children diagnosed with VVS, comprising 20 with the vasodepressor subtype, 8 with the cardioinhibitory subtype, and 12 with the mixed subtype, as well as from 60 age-matched healthy controls. Microbial community composition was assessed through 16S rRNA gene sequencing. Alpha and beta diversity analyses were conducted to evaluate differences between the VVS and HC groups, as well as among the different VVS subtypes. Then, the bacterial flora with significant differences was identified based on microbial relative abundance data using the Wilcoxon rank-sum test, ANCOM-BC2, and LEfSe analyses. Results: Compared with HCs, children with VVS exhibited reduced alpha diversity, reflected by lower Simpson and Shannon indices. Beta diversity analysis indicated a modest shift in community structure based on Bray-Curtis and weighted UniFrac distances, accompanied by increased within-group dispersion in VVS. No significant differences were detected in dominant phyla. At the genus level, among the predominant taxa, ANCOM-BC2 identified decreased Conclusion: Our findings provide evidence of gut microbiota alterations in children with VVS and suggest that reduced microbial diversity, particularly the decreased abundance of the key genera

Indexed as

BacteroidesDysbiosisGastrointestinal MicrobiomeSyncope, VasovagalAdolescentBiodiversityCase-Control StudiesChildChild, PreschoolChinaFecesFemaleHumansMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16Sautonomic nervous systemgut microbiotaorthostatic intoleranceSCFAsvasovagal syncope

Identifiers

PMID42058178
PMCPMC13121255

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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.