Causal association between rheumatoid arthritis and celiac disease: A bidirectional two-sample mendelian randomization study.

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY Frontiers in Genetics Pub Date : 2022-10-18 eCollection Date: 2022-01-01 DOI:10.3389/fgene.2022.976579
Lijiangshan Hua, Shate Xiang, Rixiang Xu, Xiao Xu, Ting Liu, Yanan Shi, Lingyun Wu, Rongyun Wang, Qiuhua Sun
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引用次数: 5

Abstract

Objectives: Rheumatoid Arthritis (RA) has been associated with Celiac Disease (CD) in previous observational epidemiological studies. However, evidence for this association is limited and inconsistent, and it remains uncertain whether the association is causal or due to confounding or reverse causality. This study aimed to assess the bidirectional causal relationship between RA and CD. Methods: In this two-sample Mendelian randomization (MR) study, instrumental variables (IVs) for RA were derived from a genome-wide association studies (GWAS) meta-analysis including 58,284 subjects. Summary statistics for CD originated from a GWAS meta-analysis with 15,283 subjects. The inverse-variance weighted (IVW) method was used as the primary analysis. Four complementary methods were applied, including the weighted-median, weighted mode, MR pleiotropy residual sum and outlier (MR-PRESSO) test and MR-Egger regression, to strengthen the effect estimates. Results: Positive causal effects of genetically increased RA risk on CD were derived [IVW odds ratio (OR): 1.46, 95% confidence interval (CI): 1.19-1.79, p = 3.21E-04]. The results of reverse MR analysis demonstrated no significant causal effect of CD on RA (IVW OR: 1.05, 95% CI: 0.91-1.21, p = 0.499). According to the sensitivity analysis, horizontal pleiotropy was unlikely to distort the causal estimates. Conclusion: This study reveals a causality of RA on CD but not CD on RA among patients of European descent. This outcome suggests that the features and indicators of CD should regularly be assessed for RA patients.

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类风湿性关节炎和乳糜泻之间的因果关系:一项双向双样本孟德尔随机研究。
目的:在以往的观察性流行病学研究中,类风湿关节炎(RA)与乳糜泻(CD)相关。然而,这种关联的证据是有限和不一致的,并且仍然不确定这种关联是因果关系还是由于混淆或反向因果关系。本研究旨在评估RA和CD之间的双向因果关系。方法:在这项双样本孟德尔随机化(MR)研究中,RA的工具变量(IVs)来自全基因组关联研究(GWAS)荟萃分析,包括58,284名受试者。CD的汇总统计数据来自GWAS对15283名受试者的荟萃分析。采用反方差加权(IVW)法进行初步分析。采用加权中位数法、加权模式法、MR多效性残差和异常值(MR- presso)检验和MR- egger回归等4种互补方法加强效应估计。结果:获得了遗传增加的RA风险对CD的积极因果效应[IVW优势比(OR): 1.46, 95%可信区间(CI): 1.19-1.79, p = 3.21E-04]。反向MR分析结果显示,CD对RA无显著的因果关系(IVW OR: 1.05, 95% CI: 0.91-1.21, p = 0.499)。根据敏感性分析,水平多效性不太可能扭曲因果估计。结论:本研究揭示了欧洲血统患者中RA与CD的因果关系,而不是CD与RA的因果关系。这一结果提示,RA患者应定期评估CD的特征和指标。
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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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