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基质细胞衍生因子-1α在有先兆偏头痛女性中减少。

Stromal Cell-Derived Factor-1 Alpha Is Decreased in Women With Migraine With Aura.

机构信息

Center for Stroke Research Berlin, Charité - Universitätsmedizin, Berlin, Germany.

Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.

出版信息

Headache. 2016 Sep;56(8):1274-9. doi: 10.1111/head.12839. Epub 2016 May 30.

DOI:10.1111/head.12839
PMID:27238143
Abstract

BACKGROUND

Endothelial dysfunction may contribute to the pathophysiology of migraine with aura. Stromal cell-derived factor-1 alpha (SDF-1α) is involved in the maintenance of endothelial integrity via mobilization of vascular stem cells.

OBJECTIVES

We sought to determine whether SDF-1α levels are decreased in women with MA.

METHODS

In this post hoc analysis of a case-cohort study, levels of SDF-1α were determined by enzyme-linked immunosorbent assay. Endothelial function was assessed using peripheral arterial tonometry. Arterial stiffness was assessed by fingertip tonometry derived and heart-rate-adjusted augmentation index (AI).

RESULTS

Twenty-eight women with MA and 27 age-matched healthy women were included in this study. Levels of SDF-1α were significantly lower in women with MA compared to age- and risk factor-matched healthy women (1763 ± 281 vs 2013 ± 263 pg/mL, P = 0.006). SDF-1α levels were positively correlated with AI in healthy women (r = 0.49, P = 0.009), but not in women with MA (r = 0.05, P = 0.78). SDF-1α levels were negatively correlated with CD144-positive endothelial microparticles (EMP; r = -0.31, P = .02), and activated CD62E-positive EMP (r = -0.35, P = .01).

CONCLUSION

Levels of SDF-1α are decreased in women with MA and are associated with EMPs as a surrogate marker of endothelial dysfunction. This might contribute to the pathophysiology and vascular risk in MA, but evidence from larger prospective studies is warranted.

摘要

背景

内皮功能障碍可能导致有先兆偏头痛的病理生理学变化。基质细胞衍生因子-1 阿尔法(SDF-1α)通过动员血管干细胞参与维持内皮完整性。

目的

我们旨在确定偏头痛伴先兆(MA)患者的 SDF-1α 水平是否降低。

方法

在一项病例对照研究的事后分析中,通过酶联免疫吸附试验测定 SDF-1α 水平。通过外周动脉张力测定法评估内皮功能。通过指尖张力测定法衍生和心率校正增强指数(AI)评估动脉僵硬。

结果

本研究纳入了 28 例 MA 女性和 27 例年龄匹配的健康女性。与年龄和危险因素匹配的健康女性相比,MA 女性的 SDF-1α 水平显著降低(1763±281 与 2013±263 pg/ml,P=0.006)。SDF-1α 水平与健康女性的 AI 呈正相关(r=0.49,P=0.009),但与 MA 女性无关(r=0.05,P=0.78)。SDF-1α 水平与 CD144 阳性内皮微颗粒(EMP;r=-0.31,P=0.02)和激活的 CD62E 阳性 EMP(r=-0.35,P=0.01)呈负相关。

结论

MA 女性的 SDF-1α 水平降低,与 EMP 作为内皮功能障碍的替代标志物相关。这可能有助于 MA 的病理生理学和血管风险,但需要更大规模的前瞻性研究来证实。

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