Tesfay Betel, Ashina Håkan, Christensen Rune Häckert, Al-Khazali Haidar M, Karlsson William Kristian, Amin Faisal Mohammad, Jawad Baker Nawfal, Andersen Ove, Ashina Messoud
Department of Neurology, Danish Headache Center, Copenhagen University Hospital-Rigshospitalet, Copenhagen 2600, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200, Denmark.
Brain Commun. 2025 Feb 17;7(1):fcae475. doi: 10.1093/braincomms/fcae475. eCollection 2025.
Soluble urokinase plasminogen activator receptor (suPAR) has garnered attention as a potential blood-based biomarker for low-grade chronic inflammation. However, its specific association with migraine, including its subtypes, remains to be elucidated. We sought to examine the association of plasma suPAR levels with migraine and its subtypes. In this single-centre, cross-sectional study, plasma was collected at a single time point in adults with migraine and sex-matched healthy controls from October 2020 to June 2022. The quantification of plasma suPAR levels was performed in a blinded fashion using a validated enzyme-linked immunosorbent assay. Plasma suPAR levels were compared between participants with migraine (including subgroups) and healthy controls. Plasma samples were analysed from 634 eligible participants with migraine [mean (SD) age, 44.0 (12.2) years; 568 (89.6%) females] and 154 healthy controls [mean (SD), 41.3 (11.8%) years; 132 (86%) females]. Plasma suPAR levels were 6.7% higher (95% CI: 0.1-13.6%; = 0.045, adjusted for age, sex, body mass index and smoking) in participants with migraine aura, when compared with healthy controls. Further analysis revealed no difference in plasma suPAR levels between the overall migraine group and healthy controls (3.7%; 95% CI: -0.7-8.2%; = 0.097), as well as between participants with migraine without aura and healthy controls (2.5%; 95% CI: -2.9-8.3%; = 0.81). Similarly, plasma suPAR levels did not differ across participants with episodic migraine, chronic migraine and healthy controls. Finally, we found no difference when comparing participants with migraine at time of blood sampling with participants with non-migraine headache (1.0%; 95% CI: -5.7-8.2; > 0.99), participants without headache (1.2%; 95% CI: -4.2-7.0%; > 0.99) or healthy controls (4.5%; 95% CI: -1.9-11.3%; = 0.39). Elevated plasma suPAR levels in migraine with aura indicate the presence of low-grade chronic inflammation. Future research should explore the role of suPAR in the neurobiologic underpinnings of migraine with aura.
可溶性尿激酶型纤溶酶原激活物受体(suPAR)作为一种潜在的基于血液的低度慢性炎症生物标志物已受到关注。然而,其与偏头痛(包括其亚型)的具体关联仍有待阐明。我们试图研究血浆suPAR水平与偏头痛及其亚型之间的关联。在这项单中心横断面研究中,于2020年10月至2022年6月期间在患有偏头痛的成年人及性别匹配的健康对照者的单个时间点采集血浆。使用经过验证的酶联免疫吸附测定法以盲法对血浆suPAR水平进行定量。比较了偏头痛患者(包括亚组)和健康对照者的血浆suPAR水平。对634名符合条件的偏头痛患者[平均(标准差)年龄,44.0(12.2)岁;568名(89.6%)女性]和154名健康对照者[平均(标准差),41.3(11.8%)岁;132名(86%)女性]的血浆样本进行了分析。与健康对照者相比,有偏头痛先兆的参与者血浆suPAR水平高6.7%(95%置信区间:0.1 - 13.6%;P = 0.045,经年龄、性别、体重指数和吸烟因素调整)。进一步分析显示,总体偏头痛组与健康对照者之间(3.7%;95%置信区间: - 0.7 - 8.2%;P = 0.097)以及无先兆偏头痛参与者与健康对照者之间(2.5%;95%置信区间: - 2.9 - 8.3%;P = 0.81)的血浆suPAR水平无差异。同样,发作性偏头痛、慢性偏头痛参与者与健康对照者之间的血浆suPAR水平也无差异。最后,我们发现,在血液采样时患有偏头痛的参与者与患有非偏头痛性头痛的参与者(1.0%;95%置信区间: - 5.7 - 8.2;P > 0.99)、无头痛的参与者(1.2%;95%置信区间: - 4.2 - 7.0%;P > 0.99)或健康对照者(4.5%;95%置信区间: - 1.9 - 11.3%;P = 0.39)之间进行比较时无差异。有先兆偏头痛患者血浆suPAR水平升高表明存在低度慢性炎症。未来的研究应探索suPAR在有先兆偏头痛的神经生物学基础中的作用。