Evidence map›Paper›PMID 42112324›Full record

ArticleFrontiers in immunology2026

Dysbiosis of gut microbiota and metabolomic alterations in myasthenia gravis: insights from 16S rRNA sequencing and untargeted metabolomics.

Yunan Shan, Wei Chen, Yanbin Li

Abstract read
In one paragraph

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

0numbers the graph read from it
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

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

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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

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

3 authors.

Yunan ShanDepartment of Neurology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Neuroimmunology, Shandong Key Laboratory of Rheumatic Disease and Translational Medicine, Jinan, China.
Wei ChenDepartment of Gastroenterology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yanbin LiDepartment of Neurology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Neuroimmunology, Shandong Key Laboratory of Rheumatic Disease and Translational Medicine, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Myasthenia gravis (MG) is an autoimmune disorder of neuromuscular transmission. Gut dysbiosis has been implicated in autoimmune pathogenesis, yet integrated microbial and metabolomic profiling in MG remains scarce. To characterize gut microbiota and the fecal metabolome in MG, identify diagnostic biomarkers, and explore associations between microbial taxa, metabolites, and clinical severity. Methods: Fecal samples from 29 MG patients and 10 healthy controls underwent 16S rRNA sequencing and UHPLC-Q-TOF MS metabolomics. LEfSe identified differential taxa; metabolites were screened by VIP > 1.0, Results: MG patients showed significantly reduced alpha- and beta-diversity. LEfSe identified 232 discriminative taxa, with depletion of Conclusions: MG patients exhibit a distinct profile of gut dysbiosis and metabolic disturbances. The specific microbial and metabolic biomarkers identified in this study may offer novel insights for auxiliary diagnosis of MG and guide future microbiota-targeted intervention strategies.

Indexed as

DysbiosisGastrointestinal MicrobiomeMetabolomeMetabolomicsMyasthenia GravisRNA, Ribosomal, 16SAdultAgedBiomarkersFecesFemaleHumansMaleMiddle AgedBiomarkersRNA, Ribosomal, 16S16S rRNA sequencingbile acidsbiomarkersbutanoic acidgut microbiotametabolomicsmyasthenia gravisshort-chain fatty acids

Identifiers

PMID42112324
PMCPMC13149435

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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.