Jie Shen, Qiao Ye, Fang Luo, Tianhang Yu, Jinli Miao, Wenmin Wang, Hui Yuan
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Sensitivity analyses, including MR-PRESSO and leave-one-out analysis, were conducted to ensure the robustness of our findings. After excluding SNPs with pleiotropic effects, 42 and 5 SNPs were identified as robust IVs for primary SS and MS, respectively. Our analysis revealed a significant protective effect of MS on primary SS, with IVW showing an OR of 0.896 (95% CI: 0.841-0.954, P = 0.001). No significant heterogeneity or horizontal pleiotropy was detected, supporting the reliability of the results. Our findings suggest a potential protective effect of MS against primary SS, indicating a negative causal association between these two autoimmune diseases. 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引用次数: 0
摘要
本研究旨在利用双样本孟德尔随机化(MR)分析法研究原发性斯约格伦综合征(SS)和多发性硬化症(MS)之间的因果关系,从而深入了解它们的共同机制和对治疗策略的影响。我们利用全基因组关联研究(GWAS)的数据,研究了原发性SS(1,290例病例和213,145例对照)和MS(4,888例病例和10,395例对照),研究对象仅限于欧洲血统。根据与原发性 SS 相关的基因变异选择了工具变量(IV)。主要的MR方法是反方差加权(IVW),辅以MR Egger、加权中位数、简单模式和加权模式算法,以评估MS与原发性SS之间的双向因果关系。为了确保研究结果的稳健性,我们进行了敏感性分析,包括MR-PRESSO和leave-one-out分析。在排除了具有多向效应的 SNPs 后,分别有 42 个和 5 个 SNPs 被确定为原发性 SS 和 MS 的稳健 IVs。我们的分析表明,MS 对原发性 SS 有明显的保护作用,IVW 的 OR 值为 0.896(95% CI:0.841-0.954,P = 0.001)。没有发现明显的异质性或水平多向性,这证明了研究结果的可靠性。我们的研究结果表明,MS 对原发性 SS 有潜在的保护作用,表明这两种自身免疫性疾病之间存在负因果关系。这为了解原发性 SS 和 MS 之间复杂的相互作用提供了宝贵的遗传证据,为研究和治疗干预提供了新途径。
Causal relationship between multiple sclerosis and primary Sjögren's syndrome: a two-sample mendelian randomization study.
This study aims to investigate the causal relationship between primary Sjögren's syndrome (SS) and multiple sclerosis (MS) using a two-sample Mendelian randomization (MR) analysis to provide insights into their common mechanisms and implications for therapeutic strategies. We utilized data from Genome-Wide Association Studies (GWAS) for primary SS (1,290 cases and 213,145 controls) and MS (4,888 cases and 10,395 controls), restricted to European ancestry. Instrumental variables (IVs) were selected based on genetic variants associated with primary SS. The primary MR method was Inverse Variance Weighted (IVW), supplemented by MR Egger, Weighted Median, Simple Mode, and Weighted Mode algorithms to assess the bidirectional causal relationships between MS and primary SS. Sensitivity analyses, including MR-PRESSO and leave-one-out analysis, were conducted to ensure the robustness of our findings. After excluding SNPs with pleiotropic effects, 42 and 5 SNPs were identified as robust IVs for primary SS and MS, respectively. Our analysis revealed a significant protective effect of MS on primary SS, with IVW showing an OR of 0.896 (95% CI: 0.841-0.954, P = 0.001). No significant heterogeneity or horizontal pleiotropy was detected, supporting the reliability of the results. Our findings suggest a potential protective effect of MS against primary SS, indicating a negative causal association between these two autoimmune diseases. This adds valuable genetic evidence to the understanding of the complex interplay between primary SS and MS, offering new avenues for research and therapeutic interventions.