Hua Lijiangshan, Xiang Shate, Xu Rixiang, Xu Xiao, Liu Ting, Shi Yanan, Wu Lingyun, Wang Rongyun, Sun Qiuhua
School of Nursing, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Front Genet. 2022 Oct 18;13:976579. doi: 10.3389/fgene.2022.976579. eCollection 2022.
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. 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. 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, 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, 0.499). According to the sensitivity analysis, horizontal pleiotropy was unlikely to distort the causal estimates. 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.
在以往的观察性流行病学研究中,类风湿性关节炎(RA)与乳糜泻(CD)有关联。然而,这种关联的证据有限且不一致,该关联是因果关系、还是由于混杂因素或反向因果关系导致的仍不确定。本研究旨在评估RA与CD之间的双向因果关系。在这项两样本孟德尔随机化(MR)研究中,RA的工具变量(IVs)来自一项包含58284名受试者的全基因组关联研究(GWAS)荟萃分析。CD的汇总统计数据源自一项包含15283名受试者的GWAS荟萃分析。采用逆方差加权(IVW)方法作为主要分析方法。应用了四种补充方法,包括加权中位数、加权众数、MR多效性残差和异常值(MR-PRESSO)检验以及MR-Egger回归,以加强效应估计。得出遗传上增加的RA风险对CD有正向因果效应[IVW比值比(OR):1.46,95%置信区间(CI):1.19 - 1.79,3.21E - 04]。反向MR分析结果显示CD对RA无显著因果效应(IVW OR:1.05,95% CI:0.91 - 1.21,0.499)。根据敏感性分析,水平多效性不太可能扭曲因果估计。本研究揭示了欧洲血统患者中RA对CD存在因果关系,而CD对RA不存在因果关系。这一结果表明,应对RA患者定期评估CD的特征和指标。