Department of Neurology, Leiden University Medical Center, P.O. 9600, 2300 WB, Leiden, The Netherlands.
J Headache Pain. 2023 Jun 6;24(1):64. doi: 10.1186/s10194-023-01601-5.
BACKGROUND: Migraine is a disabling neurological disorder whose diagnosis is based on clinical criteria. A shortcoming of these criteria is that they do not fully capture the underlying neurobiological factors and sex-specific complications in migraine such as cardio- and cerebrovascular disease. Biomarker research can help to improve disease characterization and identify pathophysiological mechanism underlying these comorbidities. OBJECTIVE: In this narrative review we searched for sex-specific metabolomics research to identify markers that may explain the migraine-cardiovascular disease (CVD) relationship. DISCUSSION: Large-scale plasma metabolome analyses revealed alterations in migraine. Sex-specific findings showed a less CVD-protective HDL metabolism as well as the ApoA1 lipoprotein, especially for women with migraine. To explore other possible pathophysiological pathways, we expanded our review to include inflammatory markers, endothelial and vascular markers and sex hormones. Biological sex differences may affect the pathophysiology of migraine and its complications. CONCLUSIONS: There is no general large dyslipidemia profile in migraine patients, in line with findings that the increased risk of CVD in migraine patients seems not to be due to (large artery) atherosclerosis. Sex-specific associations are indicative towards a less CVD-protective lipoprotein profile in women with migraine. Future studies into the pathophysiology of CVD and migraine need to take sex specific factors into account. By establishing the overlapping pathophysiological mechanism of migraine and CVD, and unraveling the associated effects these diseases exert on each other, better preventative measures can be identified.
背景:偏头痛是一种使人丧失能力的神经系统疾病,其诊断基于临床标准。这些标准的一个缺点是,它们不能完全捕捉偏头痛的潜在神经生物学因素和性别特异性并发症,如心血管疾病。生物标志物研究可以帮助改善疾病特征,并确定这些合并症的病理生理机制。
目的:在这篇叙述性综述中,我们搜索了性别特异性代谢组学研究,以确定可能解释偏头痛-心血管疾病(CVD)关系的标志物。
讨论:大规模的血浆代谢组分析显示偏头痛发生了变化。性别特异性发现表明,HDL 代谢和载脂蛋白 A1 脂蛋白的保护作用降低,特别是对偏头痛女性而言。为了探索其他可能的病理生理途径,我们将综述扩展到包括炎症标志物、内皮和血管标志物以及性激素。生物学性别差异可能影响偏头痛及其并发症的病理生理学。
结论:偏头痛患者没有一般的大血脂异常谱,这与偏头痛患者 CVD 风险增加似乎不是由于(大动脉)动脉粥样硬化的发现一致。偏头痛女性的脂蛋白谱保护作用降低,表明存在性别特异性关联。未来对 CVD 和偏头痛的病理生理学的研究需要考虑到性别特异性因素。通过确定偏头痛和 CVD 的重叠病理生理机制,并揭示这些疾病相互作用的相关影响,可以确定更好的预防措施。
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