Wang Jing, Zhou Qi
Reproductive Medical Center, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Br J Hosp Med (Lond). 2024 Nov 30;85(11):1-19. doi: 10.12968/hmed.2024.0478. Epub 2024 Nov 25.
The association between rheumatic immune diseases and polycystic ovary syndrome (PCOS) remains elusive. The purpose of this study was to investigate the causal relationship between rheumatic immune diseases and the risk of PCOS through a two-sample Mendelian randomization (MR) analysis. In the assessment of exposure variables, we chose systemic lupus erythematosus (SLE), polymyositis (PM), and rheumatoid arthritis (RA) as representative rheumatic immune diseases, while PCOS was designated as the outcome of interest. All data utilized in this investigation were obtained from the Medical Research Council Integrative Epidemiology Unit (MRC-IEU) database. A two-sample MR analysis was conducted using summary statistics for both the exposure and outcome variables, which were gathered from the genome-wide association study (GWAS) datasets. Single nucleotide polymorphisms (SNPs) significantly associated with rheumatic diseases were selected as instrumental variables (IVs) to estimate the causal effects on PCOS. The final results were analyzed using five MR analysis methods, namely MR-Egger, inverse variance weighted (IVW), weighted median (WM), simple mode, and weighted mode. Causal estimation of MR was primarily obtained using the IVW method. Sensitivity analyses were also conducted to evaluate pleiotropy and heterogeneity. In this two-sample MR analysis, a total of 1,000,246 participants were included. Among them, there were 647 cases of SLE, 44 cases of PM, 5539 cases of RA, and 797 cases of PCOS. The IVW approach indicated a causal relationship between RA and an increased risk of PCOS (odds ratio [OR] = 1.069, 95% confidence interval [CI] = 1.007-1.134, = 0.041). The MR-Egger intercept and Cochran's Q test ( > 0.005) further verified the stability of the MR results. However, no significant correlation was observed between the other two rheumatic immune diseases (PM and SLE) and the risk of developing PCOS (both > 0.05). This study suggests a potential causal association between RA and PCOS, while SLE and PM do not exhibit a causal association with PCOS, enhancing our comprehension of the etiological factors of PCOS and shedding light on prevention strategies for the disease. Additional research is required to elucidate the underlying biological mechanisms by which RA contributes to the progression of PCOS.
风湿免疫性疾病与多囊卵巢综合征(PCOS)之间的关联仍不明确。本研究的目的是通过两样本孟德尔随机化(MR)分析来探究风湿免疫性疾病与PCOS风险之间的因果关系。在暴露变量评估中,我们选择系统性红斑狼疮(SLE)、多发性肌炎(PM)和类风湿关节炎(RA)作为代表性的风湿免疫性疾病,而PCOS被指定为感兴趣的结局。本研究中使用的所有数据均来自医学研究理事会综合流行病学单位(MRC-IEU)数据库。使用从全基因组关联研究(GWAS)数据集中收集的暴露和结局变量的汇总统计数据进行两样本MR分析。选择与风湿性疾病显著相关的单核苷酸多态性(SNP)作为工具变量(IV),以估计对PCOS的因果效应。使用五种MR分析方法,即MR-Egger、逆方差加权(IVW)、加权中位数(WM)、简单模式和加权模式对最终结果进行分析。MR的因果估计主要使用IVW方法。还进行了敏感性分析以评估多效性和异质性。在这项两样本MR分析中,共纳入了1,000,246名参与者。其中,有SLE患者647例,PM患者44例,RA患者5539例,PCOS患者797例。IVW方法表明RA与PCOS风险增加之间存在因果关系(优势比[OR]=1.069,95%置信区间[CI]=1.007-1.134,P=0.0