{"title":"The serum proteomic profile in patients with migraine.","authors":"Yating Han, Yuan Wang, Xiajuan Zou, Huailian Guo","doi":"10.3389/fnmol.2025.1460403","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Discussion: </strong>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.</p>","PeriodicalId":12630,"journal":{"name":"Frontiers in Molecular Neuroscience","volume":"18 ","pages":"1460403"},"PeriodicalIF":3.5000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11973291/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Molecular Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnmol.2025.1460403","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: 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.
Methods: 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.
Results: 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.
Discussion: 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.
期刊介绍：
Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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