Targeting CGRP: A New Era for Migraine Treatment

被引:53
作者
Goldberg, Stephanie Wrobel [1 ]
Silberstein, Stephen David [1 ]
机构
[1] Thomas Jefferson Univ, Jefferson Headache Ctr, Dept Neurol, Philadelphia, PA 19107 USA
关键词
GENE-RELATED-PEPTIDE; ACTIVITY-MODIFYING PROTEIN-1; CORTICAL SPREADING DEPRESSION; INCREASES METABOLIC-ACTIVITY; RANDOMIZED CONTROLLED-TRIAL; CENTRAL-NERVOUS-SYSTEM; BLOOD-BRAIN-BARRIER; CALCITONIN-GENE; RECEPTOR ANTAGONIST; MONOCLONAL-ANTIBODY;
D O I
10.1007/s40263-015-0253-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Migraine is a highly prevalent headache disease that typically affects patients during their most productive years. Despite significant progress in understanding the underlying pathophysiology of this disorder, its treatment so far continues to depend on drugs that, in their majority, were not specifically designed for this purpose. The neuropeptide calcitonin gene-related peptide (CGRP) has been indicated as playing a critical role in the central and peripheral pathways leading to a migraine attack. It is not surprising that drugs designed to specifically block its action are gaining remarkable attention from researchers in the field with, at least so far, a safe risk profile. In this article, we highlight the evolution from older traditional treatments to the innovative CGRP target drugs that are revolutionizing the way to approach this debilitating neurological disease. We provide a brief introduction on pathophysiology of migraine and details on the characteristic, function, and localization of CGRP to then focus on CGRP receptor antagonists (CGRP-RAs) and CGRP monoclonal antibodies (CGRP mAbs).
引用
收藏
页码:443 / 452
页数:10
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