Investigating the causal relationship between rheumatoid arthritis and cardiovascular disease: A Mendelian randomization study.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-03-01 Epub Date: 2025-02-06 DOI:10.1007/s10067-025-07357-4
Xintong Xie, Guangliang Wei, Zhenboyang Tang, Huidong Chen, Xiru Lin, Chunyan Huang, Hao Yu, Youxian He, Mengxiang Li, Xue Zhang, Chengsong He, Yue He, Jie Chen
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引用次数: 0

Abstract

Objective: Previous research has revealed a positive correlation between rheumatoid arthritis (RA) and cardiovascular diseases, but the causal relationship is unclear. This study applies Mendelian randomization to examine whether RA causally contributes to the likelihood of various cardiovascular diseases, such as heart failure, coronary artery disease, and atrial fibrillation.

Methods: Using genome-wide association data, we conducted a univariable MR (UVMR) analysis to evaluate the causal impact of RA on CVD, primarily utilizing the inverse variance weighted method. Additional MR methods were used to test the robustness of the results. Multivariable MR (MVMR) was applied to explore potential confounders.

Results: In the European population, genetically predicted RA had a harmful causal effect on HF, with the IVW analysis indicating an OR of 1.06 (95% CI: 1.02-1.10, P < 0.01) based on 23 SNPs. No causal relationships were found between RA and other CVDs. The MVMR analysis did not identify significant causal impact of rheumatoid arthritis on HF after controlling for traditional risk factors. In the Asian population, RA was associated with an adverse effect on AF, with the IVW method reporting an OR of 1.20 (95% CI: 1.01-1.41, P = 0.03) for 5 SNPs. No other CVD relationships were found.

Conclusions: Our MR analysis indicates that genetic susceptibility to rheumatoid arthritis increases the likelihood of heart failure in European populations and atrial fibrillation in East Asian populations. However, established CVD risk factors, such as smoking, overweight, and physical inactivity, remain critically important in the management of RA. Key Points • Multiple studies have highlighted a marked increase in the cardiovascular event risk among individuals with RA. However, additional RCTs are needed for confirmation. • We applied Mendelian randomization to explore the potential causal relationship between rheumatoid arthritis and cardiovascular conditions. The findings demonstrated a causal link between RA and heart failure among European populations, as well as an association between RA and atrial fibrillation in East Asian groups. • Further adjustments using multivariable Mendelian randomization to account for the influence of traditional cardiovascular risk factors revealed that the causal association between RA and heart failure disappeared.

类风湿关节炎和心血管疾病之间的因果关系:一项孟德尔随机研究
目的:既往研究发现类风湿关节炎(RA)与心血管疾病呈正相关,但因果关系尚不清楚。本研究应用孟德尔随机化来研究RA是否与各种心血管疾病(如心力衰竭、冠状动脉疾病和心房颤动)的可能性有因果关系。方法:利用全基因组关联数据,我们进行了单变量MR (UVMR)分析,主要利用逆方差加权法来评估RA对CVD的因果影响。额外的MR方法被用来检验结果的稳健性。采用多变量磁共振(MVMR)分析潜在的混杂因素。结果:在欧洲人群中,遗传预测的RA对HF有有害的因果影响,IVW分析显示OR为1.06 (95% CI: 1.02-1.10, P)。结论:我们的MR分析表明,类风湿关节炎的遗传易感性增加了欧洲人群心力衰竭和东亚人群房颤的可能性。然而,已确定的心血管疾病危险因素,如吸烟、超重和缺乏身体活动,在类风湿关节炎的管理中仍然至关重要。•多项研究强调RA患者心血管事件风险显著增加。然而,需要更多的随机对照试验来证实。•我们应用孟德尔随机化来探索类风湿关节炎和心血管疾病之间的潜在因果关系。研究结果表明,在欧洲人群中,类风湿关节炎和心力衰竭之间存在因果关系,在东亚人群中,类风湿关节炎和房颤之间也存在关联。•使用多变量孟德尔随机化进一步调整,以解释传统心血管危险因素的影响,发现类风湿关节炎和心力衰竭之间的因果关系消失。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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