1 Danish Headache Center and Department of Neurology, Rigshospitalet Glostrup, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
2 Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Cephalalgia. 2019 Apr;39(5):575-584. doi: 10.1177/0333102419837154. Epub 2019 Mar 9.
To investigate the role of calcitonin gene-related peptide, pituitary adenylate cyclase-activating polypeptide-38 (PACAP38) and vasoactive intestinal polypeptide in cluster headache, we measured these vasoactive peptides interictally and during experimentally induced cluster headache attacks.
We included patients with episodic cluster headache in an active phase (n = 9), episodic cluster headache patients in remission (n = 9) and patients with chronic cluster headache (n = 13). Cluster headache attacks were induced by infusion of calcitonin gene-related peptide (1.5 µg/min) in a randomized, double-blind, placebo controlled, two-way cross-over study. At baseline, we collected interictal blood samples from all patients and during 11 calcitonin gene-related peptide-induced cluster headache attacks.
At baseline, episodic cluster headache patients in remission had higher plasma levels of calcitonin gene-related peptide, 100.6 ± 36.3 pmol/l, compared to chronic cluster headache patients, 65.9 ± 30.5 pmol/l, ( p = 0.011). Episodic cluster headache patients in active phase had higher PACAP38 levels, 4.0 ± 0.8 pmol/l, compared to chronic cluster headache patients, 3.3 ± 0.7 pmol/l, ( p = 0.033). Baseline levels of vasoactive intestinal polypeptide did not differ between cluster headache groups. We found no attack-related increase in calcitonin gene-related peptide, PACAP38 or vasoactive intestinal polypeptide levels during calcitonin gene-related peptide-induced cluster headache attacks.
This study suggests that cluster headache disease activity is associated with alterations of calcitonin gene-related peptide expression. Future studies should investigate the potential of using calcitonin gene-related peptide measurements in monitoring of disease state and predicting response to preventive treatments, including response to anti-calcitonin gene-related peptide monoclonal antibodies.
研究降钙素基因相关肽(CGRP)、垂体腺苷酸环化酶激活肽-38(PACAP38)和血管活性肠肽在丛集性头痛中的作用,我们在间歇期和实验性诱导的丛集性头痛发作期间测量了这些血管活性肽。
我们纳入了处于活跃期的发作性丛集性头痛患者(n=9)、缓解期的发作性丛集性头痛患者(n=9)和慢性丛集性头痛患者(n=13)。通过随机、双盲、安慰剂对照、双向交叉研究,以 1.5μg/min 的速度输注降钙素基因相关肽诱导丛集性头痛发作。在基线时,我们从所有患者中采集了间歇期的血样,并在 11 次降钙素基因相关肽诱导的丛集性头痛发作期间进行了采集。
在基线时,缓解期的发作性丛集性头痛患者的血浆降钙素基因相关肽水平为 100.6±36.3 pmol/l,高于慢性丛集性头痛患者的 65.9±30.5 pmol/l(p=0.011)。处于活跃期的发作性丛集性头痛患者的 PACAP38 水平为 4.0±0.8 pmol/l,高于慢性丛集性头痛患者的 3.3±0.7 pmol/l(p=0.033)。丛集性头痛患者组之间的血管活性肠肽基线水平没有差异。我们没有发现降钙素基因相关肽诱导的丛集性头痛发作期间 CGRP、PACAP38 或血管活性肠肽水平的发作相关增加。
本研究表明,丛集性头痛疾病的活动与降钙素基因相关肽表达的改变有关。未来的研究应探讨使用降钙素基因相关肽测量值监测疾病状态和预测预防治疗反应(包括对降钙素基因相关肽单克隆抗体的反应)的潜力。