血浆可溶性尿激酶纤溶酶原激活剂受体浓度与先兆偏头痛的关系:一项REFORM研究。

IF 4.1 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-02-17 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcae475
Betel Tesfay, Håkan Ashina, Rune Häckert Christensen, Haidar M Al-Khazali, William Kristian Karlsson, Faisal Mohammad Amin, Baker Nawfal Jawad, Ove Andersen, Messoud Ashina
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引用次数: 0

摘要

可溶性尿激酶纤溶酶原激活物受体(suPAR)作为一种潜在的低级别慢性炎症的血液生物标志物已经引起了人们的关注。然而,其与偏头痛的具体关系,包括其亚型,仍有待阐明。我们试图检查血浆suPAR水平与偏头痛及其亚型的关系。在这项单中心横断面研究中,研究人员从2020年10月至2022年6月在单一时间点收集了偏头痛成年患者和性别匹配的健康对照组的血浆。血浆suPAR水平的定量采用盲法,采用经验证的酶联免疫吸附法。比较偏头痛患者(包括亚组)和健康对照组的血浆suPAR水平。分析了634名符合条件的偏头痛患者的血浆样本[平均(SD)年龄44.0(12.2)岁;568例(89.6%)女性)和154例健康对照[平均(SD), 41.3(11.8%)岁;132(86%)雌性]。血浆suPAR水平升高6.7% (95% CI: 0.1-13.6%;P = 0.045(调整了年龄、性别、体重指数和吸烟),与健康对照组相比。进一步分析显示,整体偏头痛组和健康对照组的血浆suPAR水平无差异(3.7%;95% ci: -0.7-8.2%;P = 0.097),无先兆偏头痛患者和健康对照组(2.5%;95% ci: -2.9-8.3%;P = 0.81)。同样,血浆suPAR水平在发作性偏头痛、慢性偏头痛和健康对照组之间没有差异。最后,我们发现在抽血时偏头痛受试者与非偏头痛受试者之间没有差异(1.0%;95% ci: -5.7-8.2;P > 0.99),无头痛受试者(1.2%;95% ci: -4.2-7.0%;P > 0.99)或健康对照组(4.5%;95% ci: -1.9-11.3%;P = 0.39)。伴有先兆的偏头痛患者血浆suPAR水平升高表明存在低级别慢性炎症。未来的研究应探索suPAR在先兆偏头痛的神经生物学基础中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of plasma soluble urokinase plasminogen activator receptor concentrations and migraine with aura: a REFORM study.

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%; P = 0.045, adjusted for age, sex, body mass index and smoking) in participants with migraine with 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%; P = 0.097), as well as between participants with migraine without aura and healthy controls (2.5%; 95% CI: -2.9-8.3%; P = 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; P > 0.99), participants without headache (1.2%; 95% CI: -4.2-7.0%; P > 0.99) or healthy controls (4.5%; 95% CI: -1.9-11.3%; P = 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.

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