CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury.

Håkan Ashina, Afrim Iljazi, Haidar M Al-Khazali, Thien Phu Do, Anna K Eigenbrodt, Eigil L Larsen, Amalie M Andersen, Kevin J Hansen, Karoline B Bräuner, Basit Ali Chaudhry, Casper E Christensen, Faisal Mohammad Amin, Henrik W Schytz
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引用次数: 6

Abstract

Objective: To ascertain whether intravenous infusion of calcitonin gene-related peptide (CGRP) can induce migraine-like headache in people with persistent post-traumatic headache attributed to mild traumatic brain injury (TBI) and no pre-existing migraine.

Methods: A non-randomized, single-arm, open-label study at a single site in Denmark. Eligible participants were aged 18 to 65 years and had a known history of persistent post-traumatic headache attributed to mild TBI for ≥ 12 months. All participants received continuous intravenous infusion of CGRP (1.5 µg/min) over 20 min. A headache diary was used to collect outcome data until 12 h after the start of CGRP infusion. The primary end point was the incidence of migraine-like headache during 12-hour observational period.

Results: A total of 60 participants completed the study protocol and provided data for the analysis of the primary end point. The median age was 32.5 (IQR, 25.5-43.0) years; 43 participants (72%) were female. Following CGRP infusion, 43 (72%) of 60 participants developed migraine-like headache during the 12-hour observational period. The median time to peak headache intensity was 40 min (IQR, 20-60), and the median peak headache intensity was 6 (IQR, 5-8) on the 11-point numeric rating scale.

Conclusion: Intravenous infusion of CGRP is a potent inducer of migraine-like headache in people with persistent post-traumatic headache attributed to mild TBI. This observation underscores the importance of CGRP in the genesis of migraine-like headache that is often experienced by individuals who are afflicted by persistent post-traumatic headache. Further research is warranted to ascertain whether other signaling molecules also contribute to the disease mechanisms underlying post-traumatic headache.

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Abstract Image

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轻度外伤性脑损伤所致持续性创伤后头痛的cgrp诱导偏头痛样头痛。
目的:探讨静脉输注降钙素基因相关肽(CGRP)是否可诱导轻度创伤性脑损伤(TBI)后持续性创伤性头痛患者发生偏头痛样头痛。方法:在丹麦进行一项非随机、单组、开放标签的研究。符合条件的参与者年龄在18至65岁之间,并且有轻度TBI引起的持续性创伤后头痛病史≥12个月。所有参与者在20分钟内连续静脉输注CGRP(1.5µg/min)。使用头痛日记收集结果数据,直到CGRP输注开始后12小时。主要终点是12小时观察期间偏头痛样头痛的发生率。结果:共有60名参与者完成了研究方案,并为主要终点的分析提供了数据。中位年龄为32.5 (IQR, 25.5-43.0)岁;43名参与者(72%)为女性。CGRP输注后,在12小时的观察期内,60名参与者中有43名(72%)出现偏头痛样头痛。达到头痛强度峰值的中位时间为40 min (IQR, 20-60),在11点数值评定量表中,头痛强度峰值的中位时间为6 (IQR, 5-8)。结论:静脉输注CGRP可有效诱导轻度TBI所致持续性创伤后头痛患者出现偏头痛样头痛。这一观察结果强调了CGRP在偏头痛样头痛发生中的重要性,这种头痛通常发生在持续性创伤后头痛患者身上。进一步的研究是必要的,以确定是否其他信号分子也有助于创伤后头痛的疾病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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