Evidence map›Paper›PMID 39932515›Full record

ArticleMolecular neurobiology2025

Serum Inflammatory Factors Levels and Risk of Myasthenia Gravis: A Bidirectional Mendelian Randomization Study.

Sun Jingjing, Huo Liang, Yu Tao

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Article in Molecular neurobiology, 2025. 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

3 authors.

Sun JingjingDepartment of Pediatrics, Shengjing Hospital of China Medical University, Sanhao Street, Heping District, Shenyang, Liaoning, China.
Huo LiangDepartment of Pediatrics, Shengjing Hospital of China Medical University, Sanhao Street, Heping District, Shenyang, Liaoning, China.
Yu TaoDepartment of Pediatrics, Shengjing Hospital of China Medical University, Sanhao Street, Heping District, Shenyang, Liaoning, China. yucm20160620@163.com.

Funding

Liaoning Province Science and Technology Plan Joint Program 2023-MSLH-391
6 · The paper itself

Abstract

Myasthenia gravis (MG) is an autoimmune disorder characterized by muscle weakness, where the role of inflammatory processes remains incompletely understood. Bidirectional Mendelian randomization (MR) provides a method to explore potential causal relationships between traits. In this bidirectional MR study, we investigated the relationship between 40 serum inflammatory factors and MG using the two-sample MR approach. The inverse variance weighted (IVW) method was the primary analytical method. Factors with P < 0.05 after false discovery rate (FDR) correction were considered to have a significant causal relationship with MG. Bayesian colocalization and functional mapping were employed to further analyze the instrumental variables. We then used reverse MR to examine potential reverse causality and validated these findings in the UK Biobank-PPP cohort. A phenome-wide association study (PheWAS) was conducted using UK Biobank and FinnGen data to evaluate the potential side effects of targeting these inflammatory factors as therapeutic interventions. Our results indicated that elevated levels of serum interleukin-10 (IL-10) were associated with a decreased risk of MG (P = 9.34E-03, OR [95% CI] = 0.52 [0.33-0.85]). Reverse MR revealed no evidence of reverse causality (P > 0.05), with further validation in the UK Biobank-PPP cohort (P = 3.81E-3, OR [95% CI] = 5.43E-02 [7.54E-03-3.91E-01]). The PheWAS outcomes showed associations of serum IL-10 levels across a broad phenotypic spectrum. Our findings suggest that IL-10 may play a protective role in the pathogenesis of MG. The absence of reverse causality highlights IL-10 as a potential therapeutic target. This study emphasizes the importance of inflammatory factors in autoimmune disorders and supports the utility of MR studies in uncovering novel therapeutic targets.

Indexed as

InflammationInflammation MediatorsMendelian Randomization AnalysisMyasthenia GravisCohort StudiesFemaleHumansInterleukin-10MaleMiddle AgedPolymorphism, Single NucleotideRisk FactorsInflammation MediatorsInterleukin-10Mendelian randomizationMyasthenia gravisPhenome-wide association studySerum inflammatory factorsSingle nucleotide polymorphism

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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.