Systemic lupus erythematosus and epilepsy: A Mendelian randomization study

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-09-28 DOI:10.1002/epi4.13058
Yang Hu, Duo Lin, Dongmei Wu, Yuqing Zhang, Gongbo Li
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Abstract

Objective

Numerous observational studies have found a relationship between systemic lupus erythematosus (SLE) and epilepsy; however, their causal relationship remains unclear. This study aimed to investigate the causal role of SLE in epilepsy or any of its subtypes using a two-sample Mendelian randomization (MR) analysis.

Methods

Single nucleotide polymorphisms (SNPs) linked to SLE were utilized as instrumental variables in MR analysis to assess their causal impact on epilepsy. The primary MR findings were derived using the inverse variance weighted (IVW) method, which was further supported by the weighted median and MR-Egger regression techniques. Additionally, sensitivity analyses, including Cochran's Q test and pleiotropy tests, were conducted to evaluate the influence of these SNPs on epilepsy, particularly looking for signs of horizontal pleiotropy and heterogeneity.

Results

We selected 43 SNPs that reached genome-wide significance from genome-wide association studies (GWASs) on SLE to serve as instrumental variables in this study. The IVW method showed no evidence to support a causal association between SLE and epilepsy (all epilepsy: odds ratio (OR) = 1.006, 95% confidence interval (CI) = 0.994–1.018; focal epilepsy: OR = 1.006, 95% CI = 0.994–1.019; generalized epilepsy: OR = 1.015, 95% CI = 0.996–1.035). Other MR complementary methods revealed consistent results. Furthermore, there was no evidence indicating heterogeneity or horizontal pleiotropy.

Significance

The findings of MR analysis did not support a genetically predicted causal relationship between SLE and epilepsy, but emphasized the need for further research on shared pathophysiological mechanisms, particularly the role of immune system abnormalities and potential influences such as chronic inflammation and therapeutic interventions.

Plain Language Summary

The etiology of epilepsy is complex and diverse, including immune factors. Through a Mendelian randomization analysis, we did not find evidence of a genetic causal relationship between systemic lupus erythematosus and epilepsy. However, this does not invalidate epidemiological evidence, and further exploration is needed to investigate factors influencing the relationship between the two.

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系统性红斑狼疮与癫痫:孟德尔随机研究
目的:许多观察性研究发现系统性红斑狼疮(SLE)与癫痫之间存在关系,但其因果关系仍不明确。本研究旨在使用双样本孟德尔随机分析法(MR)调查系统性红斑狼疮在癫痫或其任何亚型中的因果关系:与系统性红斑狼疮相关的单核苷酸多态性(SNPs)被用作 MR 分析的工具变量,以评估它们对癫痫的因果影响。利用反方差加权法(IVW)得出了主要的MR结果,加权中位数和MR-Egger回归技术进一步支持了这一结果。此外,我们还进行了包括 Cochran's Q 检验和多向性检验在内的敏感性分析,以评估这些 SNPs 对癫痫的影响,尤其是寻找水平多向性和异质性的迹象:我们从系统性红斑狼疮的全基因组关联研究(GWAS)中选择了43个具有全基因组意义的SNPs作为本研究的工具变量。IVW方法显示,没有证据支持系统性红斑狼疮与癫痫之间存在因果关系(所有癫痫:比值比(OR)=1.006,95% 置信区间(CI)=0.994-1.018;局灶性癫痫:比值比(OR)=1.006,95% 置信区间(CI)=0.994-1.018):OR=1.006,95% 置信区间(CI)=0.994-1.019;全身性癫痫:OR = 1.015,95% CI = 0.996-1.035)。其他磁共振补充方法显示的结果一致。此外,没有证据表明存在异质性或水平多义性:MR分析的结果并不支持系统性红斑狼疮与癫痫之间的遗传预测因果关系,但强调了进一步研究共同病理生理机制的必要性,尤其是免疫系统异常的作用以及慢性炎症和治疗干预等潜在影响因素。通过孟德尔随机分析,我们没有发现系统性红斑狼疮与癫痫之间存在遗传因果关系的证据。但是,这并不能证明流行病学证据无效,还需要进一步探讨影响两者关系的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
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