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用于治疗偏头痛的钠通道拮抗剂。

Sodium channel antagonists for the treatment of migraine.

作者信息

Chiossi Lorenza, Negro Andrea, Capi Matilde, Lionetto Luana, Martelletti Paolo

机构信息

Sapienza University of Rome, NESMOS Department , Rome , Italy.

出版信息

Expert Opin Pharmacother. 2014 Aug;15(12):1697-706. doi: 10.1517/14656566.2014.929665. Epub 2014 Jun 18.

Abstract

INTRODUCTION

Migraine has a strong social impact, influencing both quality of life and work productivity. Therapeutic approach of migraine consists of a multimodal program of pharmacotherapy and behavioral therapy in order to reduce the risk of chronification. Indications for the use of preventive therapy are three or more attacks per month, significant disability, attack duration that is > 90 min.

AREAS COVERED

In this review, studies conducted on sodium channel antagonists for the prophylaxis of migraine are selected using the International Classification of Headache Disorders (ICHD)-I and -II diagnostic criteria for migraine and are open-label and placebo-controlled studies.

EXPERT OPINION

Several sodium channel antagonists, such as valproic acid, topiramate, lamotrigine, zonisamide, carbamazepine and oxcarbazepine, are widely used in migraine although without similar level of efficacy. Among these antiepileptic drugs, valproic acid and topiramate seem to be more effective in migraine, as reported in the majority of controlled studies. In spite of their high efficacy rate, important side effects should be always monitored, especially depression, cognitive functions, weight gain, sleepiness and dizziness. The usefulness of this class drug will be dramatically improved by using ongoing data on individual pharmacogenomics profile.

摘要

引言

偏头痛具有强烈的社会影响,会影响生活质量和工作效率。偏头痛的治疗方法包括药物治疗和行为治疗的多模式方案,以降低慢性化风险。预防性治疗的指征为每月发作三次或以上、严重残疾、发作持续时间>90分钟。

涵盖领域

在本综述中,根据国际头痛疾病分类(ICHD)-I和-II偏头痛诊断标准,选择了关于钠通道拮抗剂预防偏头痛的研究,这些研究为开放标签和安慰剂对照研究。

专家意见

几种钠通道拮抗剂,如丙戊酸、托吡酯、拉莫三嗪、唑尼沙胺、卡马西平和奥卡西平,虽疗效水平不尽相同,但在偏头痛治疗中广泛应用。在这些抗癫痫药物中,如大多数对照研究报道的那样,丙戊酸和托吡酯在偏头痛治疗中似乎更有效力。尽管它们有效率较高,但应始终监测重要的副作用,尤其是抑郁、认知功能、体重增加、嗜睡和头晕。通过利用个体药物基因组学概况的现有数据,这类药物的效用将得到显著提高。

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