Shaoxing Central Hospital, The Hospital Affiliated to Shaoxing University, Shaoxing, China.
Central Laboratory, The Central Hospital of Shaoxing University, Shaoxing, China.
Headache. 2024 Jun;64(6):624-631. doi: 10.1111/head.14723. Epub 2024 Apr 28.
To assess whether systemic lupus erythematosus (SLE) may be genetically causally associated with migraine, including the two primary subtypes: migraine with aura (MWA) and migraine without aura (MWoA).
The association between SLE and migraine has been investigated extensively. Previous studies have shown a higher prevalence of migraine in patients with SLE, although the exact relationship remains unclear. This study investigated the potential causal association between SLE and migraine using the powerful analytical tool of Mendelian randomization (MR).
We performed two-sample MR analysis of publicly available summary statistic datasets using inverse variance-weighted (IVW), weighted median, and MR-Egger methods based on an SLE genome-wide association study (GWAS; 5201 cases; 9066 controls; the exposure frequency is 36.5%) as an exposure and migraine GWAS (15,905 cases; 264,662 controls) in individuals with European ancestry as outcomes, focusing on the two migraine subtypes MWA (6780 cases; 264,662 controls) and MWoA (5787 cases; 264,662 controls). Thepleiotropy and heterogeneity were performed.
We selected 42 single-nucleotide polymorphisms from SLE GWAS as instrumental variables (IVs) for SLE on migraine, and 41 SNP IVs for SLE on MWA or MWoA. The IVW (odds ratio [OR] = 1.01, 95% confidence interval [CI] = [0.99, 1.03], p = 0.271), weighted median (OR = 1.00, 95% CI = [0.97, 1.03], p = 0.914), and MR-Egger (OR = 1.04, 95% CI = [0.99, 1.09], p = 0.153) methods showed no causal effect of SLE on migraine. A causal effect of SLE was observed on MWA (IVW: OR = 1.05, 95% CI = [1.02, 1.08], p = 0.001; weighted median: OR = 1.05, 95% CI = [1.01, 1.10], p = 0.018; MR-Egger: OR = 1.07, 95% CI = [1.01, 1.14], p = 0.035 and p < 0.017 [Bonferroni correction]) but not MWoA (IVW: OR = 0.99, 95% CI = [0.96, 1.02], p = 0.331; weighted median: OR = 0.98, 95% CI = [0.94, 1.03], p = 0.496; MR-Egger: OR = 1.02, 95% CI = [0.95, 1.09], p = 0.652). The results showed no significant pleiotropy or heterogeneity.
Our MR analysis demonstrated the complex relationship between SLE and migraine, suggesting a potential effect of SLE on the risk of MWA but not MWoA. These findings can aid in the development of improved subtype-specific management of migraine in patients with SLE.
评估系统性红斑狼疮(SLE)是否可能与偏头痛存在遗传因果关系,包括偏头痛的两种主要亚型:有先兆偏头痛(MWA)和无先兆偏头痛(MWoA)。
SLE 与偏头痛之间的关联已被广泛研究。既往研究表明 SLE 患者偏头痛的患病率较高,但确切的关系仍不清楚。本研究使用孟德尔随机化(MR)这一强大的分析工具,探讨 SLE 与偏头痛之间潜在的因果关系。
我们对已公开的汇总统计数据集进行两样本 MR 分析,使用基于 SLE 全基因组关联研究(GWAS;5201 例病例;9066 例对照;暴露频率为 36.5%)的逆方差加权(IVW)、加权中位数和 MR-Egger 方法,将偏头痛 GWAS(15905 例病例;264662 例对照)作为结局,重点关注偏头痛的两种亚型 MWA(6780 例病例;264662 例对照)和 MWoA(5787 例病例;264662 例对照)。同时进行了多效性和异质性检验。
我们选择了来自 SLE GWAS 的 42 个单核苷酸多态性作为 SLE 对偏头痛的工具变量(IV),以及 41 个 SNP IV 作为 SLE 对 MWA 或 MWoA 的工具变量。IVW(比值比[OR] = 1.01,95%置信区间[CI] = [0.99,1.03],p = 0.271)、加权中位数(OR = 1.00,95% CI = [0.97,1.03],p = 0.914)和 MR-Egger(OR = 1.04,95% CI = [0.99,1.09],p = 0.153)方法均未显示 SLE 对偏头痛有因果影响。SLE 对 MWA 有因果作用(IVW:OR = 1.05,95% CI = [1.02,1.08],p = 0.001;加权中位数:OR = 1.05,95% CI = [1.01,1.10],p = 0.018;MR-Egger:OR = 1.07,95% CI = [1.01,1.14],p = 0.035 和 p < 0.017[Bonferroni 校正]),但对 MWoA 没有因果作用(IVW:OR = 0.99,95% CI = [0.96,1.02],p = 0.331;加权中位数:OR = 0.98,95% CI = [0.94,1.03],p = 0.496;MR-Egger:OR = 1.02,95% CI = [0.95,1.09],p = 0.652)。结果未显示出显著的多效性或异质性。
本 MR 分析表明 SLE 与偏头痛之间存在复杂的关系,提示 SLE 可能对 MWA 的风险有潜在影响,但对 MWoA 没有影响。这些发现有助于改善 SLE 患者偏头痛的亚型特异性管理。