Han Yating, Wang Yuan, Zou Xiajuan, Guo Huailian
Department of Neurology, Peking University People's Hospital, Beijing, China.
Synthetic and Functional Biomolecules Center, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing, China.
Front Mol Neurosci. 2025 Mar 24;18:1460403. doi: 10.3389/fnmol.2025.1460403. eCollection 2025.
Migraine is a paroxysmal headache disorder, which seriously affects the patients' quality of life. However, the pathogenesis of migraine is not clear yet. Proteomics is an emerging technology for studying small molecules and protein components in biological systems. This study aimed to analyze the serum proteome of migraine patients and healthy controls and identify differentially expressed proteins, which could provide a reference for the study of biomarkers and pathophysiological mechanisms of migraine.
Fasting venous blood was collected, and serum was separated. Liquid chromatography-mass spectrometry was used to detect the proteome of the two groups, and MaxQuant was used to analyze the protein profile and identify the differentially expressed proteins.
Twenty-seven migraine patients and 20 healthy people matching the age and sex ratio of the migraine group were collected. A total of 27 differentially expressed proteins were identified between migraine and control groups, which were mainly related to immune response, inflammation, glycolysis, lipid metabolism, neurotrophy and development, and so on. Subgroup analysis also identified several differentially expressed proteins between the migraine with aura and the migraine without aura groups and between the ictal and interictal migraine groups. Moreover, the signal pathways that may be related to migraine include the glycolysis/gluconeogenesis pathway and the hypoxia-inducible factor-1 signal pathway. Differentially expressed proteins are mainly distributed in the extracellular area. Related biological processes include complement activation, immunoglobulin receptor binding, and phagocytosis.
The research screened out several differentially expressed proteins of migraine patients, which may be potential biomarkers, but it still needs verification in further studies with larger sample sizes. Various proteins related to inflammation, immune response, and energy metabolism are differentially expressed between the migraine group and the control group, suggesting that the pathogenesis of migraine may be related to inflammation, immunity, and energy metabolism disorders. In the future, we can further explore the therapeutic targets of migraine in terms of these biological processes.
偏头痛是一种发作性头痛疾病,严重影响患者生活质量。然而,偏头痛的发病机制尚不清楚。蛋白质组学是研究生物系统中小分子和蛋白质成分的新兴技术。本研究旨在分析偏头痛患者和健康对照者的血清蛋白质组,鉴定差异表达蛋白,为偏头痛生物标志物及病理生理机制的研究提供参考。
采集空腹静脉血,分离血清。采用液相色谱 - 质谱联用技术检测两组的蛋白质组,并用MaxQuant分析蛋白质图谱,鉴定差异表达蛋白。
收集了27例偏头痛患者和20例年龄及性别比例与偏头痛组匹配的健康人。偏头痛组与对照组之间共鉴定出27种差异表达蛋白,主要与免疫反应、炎症、糖酵解、脂质代谢、神经营养和发育等有关。亚组分析还鉴定出有先兆偏头痛组与无先兆偏头痛组之间以及发作期与发作间期偏头痛组之间的几种差异表达蛋白。此外,可能与偏头痛相关的信号通路包括糖酵解/糖异生途径和缺氧诱导因子 - 1信号通路。差异表达蛋白主要分布在细胞外区域。相关生物学过程包括补体激活、免疫球蛋白受体结合和吞噬作用。
本研究筛选出偏头痛患者的几种差异表达蛋白,可能是潜在的生物标志物,但仍需在更大样本量的进一步研究中进行验证。偏头痛组与对照组之间多种与炎症、免疫反应和能量代谢相关的蛋白质存在差异表达,提示偏头痛的发病机制可能与炎症、免疫及能量代谢紊乱有关。未来可从这些生物学过程进一步探索偏头痛的治疗靶点。