Tfelt-Hansen Peer, Le Han
Department of Neurology, Danish Headache Centre, Glostrup Hospital, University of Copenhagen, Glostrup, Denmark.
J Headache Pain. 2009 Jun;10(3):137-43. doi: 10.1007/s10194-009-0112-8. Epub 2009 Mar 28.
The involvement of calcitonin gene-related peptide (CGRP) in migraine pathophysiological mechanisms is shown by the facts that CGRP can induce migraine and that two CGRP antagonists, olcegepant and telcagepant, are effective in the treatment of migraine attacks. Increase of the neuropeptide CGRP during migraine and cluster headache attacks in the extracerebral circulation as measured in the external jugular vein (EJV) has been regarded as an established fact. Then in 2005, a study, using the migraine patients as their own controls, showed; however, no changes of CGRP in EJV. For migraine there is thus some uncertainty as to whether CGRP is increased in all migraine patients and more research is needed. In contrast, there are three 'positive' studies in cluster headache in which both sumatriptan, O(2) and spontaneous resolution normalized CGRP. The source of an increase of CGRP in EJV is most likely a 'nervous vasodilatory drive' in the extracranial vascular bed. It remains an enigma how the observed increase of CGRP in the EJV fits into the mechanisms of migraine and cluster headache.
降钙素基因相关肽(CGRP)参与偏头痛病理生理机制的证据如下:CGRP可诱发偏头痛,且两种CGRP拮抗剂olcegepant和telcagepant对偏头痛发作的治疗有效。通过测量颈外静脉(EJV)发现,偏头痛和丛集性头痛发作期间脑外循环中神经肽CGRP增加,这已被视为既定事实。然而,2005年的一项以偏头痛患者自身作为对照的研究显示,EJV中的CGRP并无变化。因此,对于所有偏头痛患者CGRP是否都会增加仍存在一些不确定性,还需要更多研究。相比之下,有三项关于丛集性头痛的“阳性”研究表明,舒马曲坦、氧气和自然缓解均使CGRP恢复正常。EJV中CGRP增加的来源很可能是颅外血管床的“神经血管舒张驱动”。EJV中观察到的CGRP增加如何与偏头痛和丛集性头痛的机制相契合,仍是一个谜。