Evidence map›Paper›PMID 42787195›Full record

ArticleFrontiers in immunology2026

Oral microbiota and serum metabolomics features in newly diagnosed anti-AchR antibody-positive myasthenia gravis patients.

Chao Huang, Zhihui Duan, Yan Li, RuiHua Liu, Dandan Shang, Yunting Zhang, Yi Liu, Yuao Wang, Xue Zhao, Yunke Zhang and 1 more

Abstract read
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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.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Chao HuangDepartment of Encephalopathy, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Zhihui DuanDepartment of Neurology, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang Cerebrovascular Disease (Stroke) Clinical Medical Research Center, Regional Medical Center for Neurological Diseases of Henan Province, Luoyang Key Laboratory of Multi-omics Research and Application in Neurological Diseases, Luoyang, China.
Yan LiDepartment of Neurology, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang Cerebrovascular Disease (Stroke) Clinical Medical Research Center, Regional Medical Center for Neurological Diseases of Henan Province, Luoyang Key Laboratory of Multi-omics Research and Application in Neurological Diseases, Luoyang, China.
RuiHua LiuDepartment of Neurology, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang Cerebrovascular Disease (Stroke) Clinical Medical Research Center, Regional Medical Center for Neurological Diseases of Henan Province, Luoyang Key Laboratory of Multi-omics Research and Application in Neurological Diseases, Luoyang, China.
Dandan ShangDepartment of Neurology, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang Cerebrovascular Disease (Stroke) Clinical Medical Research Center, Regional Medical Center for Neurological Diseases of Henan Province, Luoyang Key Laboratory of Multi-omics Research and Application in Neurological Diseases, Luoyang, China.
Yunting ZhangDepartment of Neurology, Henan Medical University, Xinxiang, China.
Yi LiuDepartment of Neurology, Henan Medical University, Xinxiang, China.
Yuao WangDepartment of Neurology, Henan Medical University, Xinxiang, China.
Xue ZhaoDepartment of Neuroimmunology, Henan Institute of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China.
Yunke ZhangDepartment of Encephalopathy, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Feng GaoDepartment of Neuroimmunology, Henan Institute of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Myasthenia gravis (MG) is an autoimmune disorder mediated by autoantibodies. While research regarding the microbiota-gut-brain axis has expanded significantly in recent years, the role of the oral microbiota in MG and its potential association with systemic metabolism remain poorly understood. To address this, we conducted a case-control study to investigate potential alterations in the oral microbiota and serum metabolites in newly diagnosed and treatment-naïve patients with MG. Methods: In total, 38 newly diagnosed and treatment-naïve anti-AchR antibody-positive MG patients were recruited, including 19 with ocular myasthenia gravis (OMG) and 19 with generalized myasthenia gravis (GMG), along with 29 healthy controls (HCs). Saliva and serum samples were collected for 16S rRNA gene high-throughput sequencing and untargeted metabolomic profiling, respectively. Data processing and integration were performed using multiple bioinformatics and statistical methods, including α- and β-diversity analyses, LEfSe, Spearman correlation, and metabolic pathway enrichment analysis. Results: Compared with HCs, patients with OMG and GMG exhibited significant dysbiosis. At the phylum level, the abundance of Bacillota was significantly increased, whereas that of Bacteroidota and Campylobacterota was significantly decreased. At the genus level, the abundances of Conclusions: In MG patients, significant oral dysbiosis may be associated with MG-related metabolic alterations by disrupting metabolic pathways, such as those associated with lipid and amino acid metabolism.

Indexed as

AutoantibodiesMetabolomeMicrobiotaMouthMyasthenia GravisReceptors, CholinergicAdultBiomarkersCase-Control StudiesDysbiosisFemaleHumansMaleMetabolomicsMiddle AgedRNA, Ribosomal, 16SAutoantibodiesBiomarkersReceptors, CholinergicRNA, Ribosomal, 16S16S rRNAbiomarkermetabolomicsmyasthenia gravisoral microbiota

Identifiers

PMID42787195
PMCPMC13600887

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