降钙素基因相关肽
偏头痛
医学
耐受性
降钙素
药理学
单克隆抗体
内科学
受体
免疫学
不利影响
神经肽
抗体
作者
Edoardo Caronna,Alicia Alpuente,Marta Torres‐Ferrús,Patricia Pozo‐Rosich
出处
期刊:Handbook of Clinical Neurology
[Elsevier BV]
日期:2024-01-01
卷期号:: 107-124
被引量:9
标识
DOI:10.1016/b978-0-12-823357-3.00024-0
摘要
Migraine is a prevalent and disabling neurological disease. Its preventive treatment for decades has been rather limited due to the absence of disease-specific therapies with limited efficacy and tolerability. The advances made in migraine research have led to the discovery of the calcitonin gene-related peptide (CGRP) and its role in migraine pathophysiology. CGRP is a neuropeptide that acts as potent vasodilator and is involved in pain processing. Increased levels of plasma CGRP have been observed during migraine attacks as well as interictally when comparing patients with migraine and healthy controls. In the last years, two classes of drugs antagonizing CGRP have therefore been developed as the first migraine-specific preventive treatments: anti-CGRP monoclonal antibodies (mAbs) and gepants. Four mAbs have been approved: erenumab, galcanezumab, fremanezumab, and eptinezumab. Gepants are small molecules that antagonize the CGRP receptor; currently only rimegepant and atogepant have been approved for migraine prevention. These new drugs have demonstrated efficacy and safety in clinical trials for both episodic and chronic migraine, and results from their real-world experience are being increasingly reported in literature. In this review, we provide an overview of anti-CGRP drugs and their placement in migraine prevention.
科研通智能强力驱动
Strongly Powered by AbleSci AI