偏头痛
医学
西地那非
降钙素基因相关肽
苏马曲普坦
安慰剂
麻醉
内科学
降钙素
药理学
内分泌学
受体
神经肽
兴奋剂
病理
替代医学
作者
Bianca Raffaelli,Thien Phu,Håkan Ashina,Josefin Snellman,Tina Maio‐Twofoot,Messoud Ashina
出处
期刊:Cephalalgia
[SAGE Publishing]
日期:2024-06-01
卷期号:44 (6)
被引量:3
标识
DOI:10.1177/03331024241259489
摘要
Background The cAMP and cGMP pathways are implicated in the initiation of migraine attacks, but their interactions remain unclear. Calcitonin gene-related peptide (CGRP) triggers migraine attacks via cAMP, whereas the phosphodiesterase-5 inhibitor sildenafil induces migraine attacks via cGMP. Our objective was to investigate whether sildenafil could induce migraine attacks in individuals with migraine pre-treated with the CGRP-receptor antibody erenumab. Methods In this randomized, double-blind, placebo-controlled, cross-over study, adults with migraine without aura received a single subcutaneous injection of 140 mg erenumab on day 1. They were then randomized to receive sildenafil 100 mg or placebo on two experimental days, each separated by at least one week, between days 8 and 21. The primary endpoint was the difference in the incidence of migraine attacks between sildenafil and placebo during the 12-h observation period after administration. Results In total, 16 participants completed the study. Ten participants (63%) experienced a migraine attack within 12 h after sildenafil administration compared to three (19%) after placebo ( p = 0.016). The median headache intensity was higher after sildenafil than after placebo (area under the curve (AUC) for the 12-h observation period, p = 0.026). Furthermore, sildenafil induced a significant decrease in mean arterial blood pressure (AUC, p = 0.026) and a simultaneous increase in heart rate (AUC, p < 0.001) during the first hour after administration compared to placebo. Conclusion These findings provide evidence that migraine induction via the cGMP pathway can occur even under CGRP receptor blockade. Trial registration ClinicalTrials.gov: Identifier NCT05889455.
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