Xing Xiuye, Wei Dachao, Lu Qun
Medical Center for Human Reproduction, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Am J Reprod Immunol. 2025 May;93(5):e70083. doi: 10.1111/aji.70083.
Polycystic ovary syndrome (PCOS) is known to be associated with immune response dysregulation, resembling autoimmune diseases. However, the causal relationship between PCOS and autoimmune diseases remains unclear.
A two-sample bidirectional Mendelian randomization (MR) analysis was conducted using publicly available genome-wide association study (GWAS) data. The primary causal effects were estimated using the inverse-variance weighted (IVW) method, complemented by the weighted median, weighted mode, and MR-Egger regression approaches. Horizontal pleiotropy was assessed using MR-Egger regression and the MR pleiotropy residual sum and outlier (MR-PRESSO) method. Additionally, bidirectional MR analysis was performed to determine the directionality of causal relationships.
IVW analysis revealed no causal inference of PCOS on autoimmune diseases (odds ratios [OR]: 0.93-1.19, p > 0.05), and no evidence of a causal relationship was observed between autoimmune diseases and PCOS (OR 0.98-1.11, p > 0.05). These findings were further supported by the weighted median and mode methods. However, MR-Egger analysis suggested potential causal associations between rheumatoid arthritis (RA), Crohn's disease (CD), and inflammatory bowel disease (IBD) with PCOS (OR: 0.87-1.08, p < 0.05), though horizontal pleiotropy was detected for RA and IBD, indicating potential bias.
Genetically predicted PCOS was not causally linked to autoimmune diseases. Although potential associations between RA, CD, and IBD with PCOS were identified, these results should be interpreted cautiously due to possible pleiotropy. Future studies with larger sample sizes and advanced MR methodologies are warranted to validate these findings.
多囊卵巢综合征(PCOS)已知与免疫反应失调有关,类似于自身免疫性疾病。然而,PCOS与自身免疫性疾病之间的因果关系仍不清楚。
使用公开可用的全基因组关联研究(GWAS)数据进行两样本双向孟德尔随机化(MR)分析。使用逆方差加权(IVW)方法估计主要因果效应,并辅以加权中位数、加权众数和MR-Egger回归方法。使用MR-Egger回归和MR多效性残差和异常值(MR-PRESSO)方法评估水平多效性。此外,进行双向MR分析以确定因果关系的方向性。
IVW分析显示PCOS对自身免疫性疾病无因果推断(优势比[OR]:0.93-1.19,p>0.05),且未观察到自身免疫性疾病与PCOS之间存在因果关系的证据(OR 0.98-1.11,p>0.05)。加权中位数和众数方法进一步支持了这些发现。然而,MR-Egger分析表明类风湿性关节炎(RA)、克罗恩病(CD)和炎症性肠病(IBD)与PCOS之间存在潜在因果关联(OR:0.87-1.08,p<0.05),尽管检测到RA和IBD存在水平多效性,表明存在潜在偏倚。
遗传预测的PCOS与自身免疫性疾病无因果关系。虽然确定了RA、CD和IBD与PCOS之间存在潜在关联,但由于可能存在多效性,这些结果应谨慎解释。有必要开展样本量更大、采用先进MR方法的未来研究来验证这些发现。