孟德尔随机化
医学
优势比
因果关系(物理学)
单核苷酸多态性
偏头痛
观察研究
荟萃分析
置信区间
生物信息学
内科学
遗传学
生物
遗传变异
基因
基因型
物理
量子力学
作者
Yang Wang,Xiaofang Hu,Xiaoqing Wang,Lili Li,Ping Lou,Zhaoxuan Liu
出处
期刊:Thrombosis and Haemostasis
[Georg Thieme Verlag KG]
日期:2024-04-24
摘要
Background: The objective of this study is to utilize Mendelian Randomization to scrutinize the mutual causality between migraine and Venous Thromboembolism (VTE) thereby addressing the heterogeneity and inconsistency that were observed in prior observational studies concerning the potential interrelation of the two conditions. Methods: Employing a bidirectional Mendelian Randomization approach, the study explored the link between migraine and VTE, incorporating participants of European descent from a large-scale meta-analysis. An inverse-variance weighted (IVW) regression model, with random-effects, leveraging Single-Nucleotide Polymorphisms (SNPs) as instrumental variables was utilized to endorse the mutual causality between migraine and VTE. SNP heterogeneity was evaluated using Cochran’s Q-test and to account for multiple testing, correction was implemented using the intercept of the MR-Egger method, and a leave-one-out analysis. Results: The IVW model unveiled a statistically considerable causal link between migraine and the development of VTE (odds ratio [OR] = 96.155, 95% confidence interval [CI]: 4.342-2129.458, P = 0.004), implying that migraine poses a strong-risk factor for VTE development. Conversely, both IVW and simple model outcomes indicated that VTE poses as a weaker-risk factor for migraine (IVW OR = 1.002, 95% CI: 1.000-1.004, P = 0.016). The MR-Egger regression analysis denoted absence of evidence for genetic pleiotropy among the SNPs while the durability of our Mendelian Randomization results was vouched by the leave-one-out sensitivity analysis. Conclusion: The findings of this Mendelian Randomization assessment provide substantiation for a reciprocal causative association between migraine and VTE within the European population.
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