Department of Neurology, Xuanwu Hospital, Capital Medical University, National Center for Neurological Disorders, Beijing, People's Republic of China.
Department of Cardiology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Brain Behav. 2024 Feb;14(2):e3417. doi: 10.1002/brb3.3417.
Numerous studies have found that patients with systemic lupus erythematosus (SLE) often have comorbid headache, especially migraine. However, the causal relationship between genetically determined SLE and migraine risk remains unclear. Therefore, we conducted a Mendelian randomization (MR) study to explore this causal association.
Genome-wide association studies (GWAS) provided the instrumental variables. We selected summary data from GWAS of SLE as exposure (5201 SLE patients and 9066 controls). Both outcome GWAS data were from the Finnish Gene GWAS, including migraine with aura, migraine with aura and triptan purchases, and migraine without aura. The main MR approach was inverse-variance weighted. Pleiotropy and heterogeneity were detected using the MR pleiotropy residual sum and outlier, MR-Egger intercept test, leave-one-out analysis, and Cochran's Q test.
There was a significant association between genetically predicted SLE susceptibility and increased risk of migraine with aura [odds ratio (OR) = 1.05, 95% confidence interval (CI) = 1.02-1.08, p = .001]. The result was consistent when the outcome was migraine with aura and triptan purchases [OR = 1.05, 95% CI = 1.02-1.08, p = .001]. However, we found no association between SLE and migraine without aura. Our MR study showed no pleiotropy or heterogeneity.
Our study indicates that genetic susceptibility to SLE increases the incidence of migraine with aura but not migraine without aura. It is necessary for the routine evaluation and early recognition of migraine in patients with SLE in clinical settings.
大量研究发现,系统性红斑狼疮(SLE)患者常伴有共病性头痛,尤其是偏头痛。然而,遗传决定的 SLE 与偏头痛风险之间的因果关系尚不清楚。因此,我们进行了一项孟德尔随机化(MR)研究来探讨这种因果关系。
全基因组关联研究(GWAS)提供了工具变量。我们选择了 SLE GWAS 的汇总数据作为暴露因素(5201 例 SLE 患者和 9066 例对照)。结局 GWAS 数据均来自芬兰基因 GWAS,包括有先兆偏头痛、有先兆偏头痛和曲普坦购买、无先兆偏头痛。主要的 MR 方法是逆方差加权。使用 MR 多效性残差和异常值、MR-Egger 截距检验、单样本分析和 Cochran's Q 检验来检测多效性和异质性。
遗传预测的 SLE 易感性与有先兆偏头痛风险增加之间存在显著关联[比值比(OR)=1.05,95%置信区间(CI)=1.02-1.08,p=0.001]。当结局为有先兆偏头痛和曲普坦购买时,结果是一致的[OR=1.05,95% CI=1.02-1.08,p=0.001]。然而,我们没有发现 SLE 与无先兆偏头痛之间的关联。我们的 MR 研究没有发现多效性或异质性。
我们的研究表明,SLE 的遗传易感性增加了有先兆偏头痛的发生率,但不会增加无先兆偏头痛的发生率。在临床环境中,有必要对 SLE 患者进行偏头痛的常规评估和早期识别。