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The Gut Microbiome and Osteoarthritis: A Two-Sample Mendelian Randomization StudyThe Gut Microbiome and Osteoarthritis: A Two-Sample Mendelian Randomization Study

Other Titles
The Gut Microbiome and Osteoarthritis: A Two-Sample Mendelian Randomization Study
Authors
이영호송관규
Issue Date
2021
Publisher
대한류마티스학회
Keywords
Gut microbiome; Osteoarthritis; Mendelian randomization analysis
Citation
대한류마티스학회지, v.28, no.2, pp.94 - 100
Indexed
KCI
Journal Title
대한류마티스학회지
Volume
28
Number
2
Start Page
94
End Page
100
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/129795
DOI
10.4078/jrd.2021.28.2.94
ISSN
2093-940X
Abstract
Objective. The aim of this study was to examine if the intestinal microbiome is causally correlated with osteoarthritis (OA) incidence. Methods. A two-sample Mendelian randomization (MR) study was conducted using inverse variance weighting (IVW), weighted median, and MR-Egger regression techniques. Publicly accessible summary statistics dataset of intestinal microbiomes of European descent from genome-wide association studies (GWASs) (a total with 3,326 individuals) was used as an exposure. As an outcome, summary data from the GWAS include 3,498 patients with OA of the knee and hip from the arcOGEN sample and 11,009 controls of European descent. Results. We identified 29 single-nucleotide polymorphisms from GWAS of intestinal microbiomes as instrumental variables. The IVW approach found no evidence to suggest a causal relationship between the intestinal microbiota and OA (beta=−0.001, standard error [SE]=0.004, p=0.748). The regression test of MR-Egger showed that the directional pleiotropy was unlikely to be a bias (intercept=0.002, SE=0.007, p=0.697) and the MR-Egger study showed no causal relation between the intestinal microbiota and the OA (beta=−0.002, SE=0.005, p=0.630). The weighted median analysis also did not have indications of a causal relationship between the intestinal microbiota and OA (beta=−0.002, SE=0.005, p=0.630). The MR results calculated using IVW, the median weighted and the MR-Egger regression approaches were consistent. Conclusion. The findings of the MR analysis did not support a causal relationship between intestinal microbiome and OA risk.
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