Causal Effects between Gut Microbiome and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Two-Sample Mendelian Randomization Study

被引:9
作者
He, Gang [1 ]
Cao, Yu [1 ]
Ma, Honghao [1 ]
Guo, Siran [2 ]
Xu, Wangzi [1 ]
Wang, Dai [1 ]
Chen, Yongquan [3 ]
Wang, Houzhao [1 ,3 ]
机构
[1] Xiamen Univ, Sch Publ Hlth, State Key Lab Mol Vaccinol & Mol Diagnost, Xiamen, Peoples R China
[2] Yunnan Univ Tradit Chinese Med, Yunnan Prov Key Lab Mol Biol Sinomedicine, Kunming, Yunnan, Peoples R China
[3] Xiamen Univ, Xiangan Hosp, Dept Clin Lab, Xiamen, Fujian, Peoples R China
关键词
gut microbiota; mendelian randomization; Myalgia Encephalomyelitis; Chronic Fatigue Syndrome; causal relationship; gut microbiome; CONTRIBUTE; INFERENCE;
D O I
10.3389/fmicb.2023.1190894
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundEvidence from previous studies have implicated an important association between gut microbiota (GM) and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), but whether there is a definite causal relationship between GM and ME/CFS has not been elucidated. MethodThis study obtained instrumental variables of 211 GM taxa from the Genome Wide Association Study (GWAS), and mendelian randomization (MR) study was carried out to assess the effect of gut microbiota on ME/CFS risk from UK Biobank GWAS (2076 ME/CFS cases and 460,857 controls). Inverse variance weighted (IVW) was the primary method to analyze causality in this study, and a series of sensitivity analyses was performed to validate the robustness of the results. ResultsThe inverse variance weighted (IVW) method indicated that genus Paraprevotella (OR:1.001, 95%CI:1.000-1.003, value of p < 0.05) and Ruminococca- ceae_UCG_014 (OR 1.003, 95% CI 1.000 to 1.005, value of p < 0.05) were positively associated with ME/CFS risk. Results from the weighted median method supported genus Paraprevotella (OR 1.003, 95% CI 1.000 to 1.005, value of p < 0.05) as a risk factor for ME/CFS. ConclusionThis study reveals a causal relationship between genus paraprevotella, genus Ruminococcaceae_UCG_014 and ME/CFS, and our findings provide novel insights for further elucidating the developmental mechanisms mediated by the gut microbiota of ME/CFS.
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页数:7
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