Intervening in the Premonitory Phase to Prevent Migraine: Prospects for Pharmacotherapy.

IF 7.4 2区 医学 Q1 CLINICAL NEUROLOGY CNS drugs Pub Date : 2024-07-01 Epub Date: 2024-05-31 DOI:10.1007/s40263-024-01091-2
Nazia Karsan, Peter J Goadsby
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Abstract

Migraine is a common brain condition characterised by disabling attacks of headache with sensory sensitivities. Despite increasing understanding of migraine neurobiology and the impacts of this on therapeutic developments, there remains a need for treatment options for patients underserved by currently available therapies. The first specific drugs developed to treat migraine acutely, the serotonin-5-hydroxytryptamine [5-HT1B/1D] receptor agonists (triptans), seem to require headache onset in order to have an effect, while early treatment during mild pain before headache escalation improves short-term and long-term outcomes. Some patients find treating in the early window once headache has started but not escalated difficult, and migraine can arise from sleep or in the early hours of the morning, making prompt treatment after pain onset challenging. Triptans may be deemed unsuitable for use in patients with vascular disease and in those of older age and may not be effective in a proportion of patients. Headache is also increasingly recognised as being just one of the many facets of the migraine attack, and for some patients it is not the most disabling symptom. In many patients, painless symptoms can start prior to headache onset and can reliably warn of impending headache. There is, therefore, a need to identify therapeutic targets and agents that may be used as early as possible in the course of the attack, to prevent headache onset before it starts, and to reduce both headache and non-headache related attack burden. Early small studies using domperidone, naratriptan and dihydroergotamine have suggested that this approach could be useful; these studies were methodologically less rigorous than modern day treatment studies, of small sample size, and have not since been replicated. The emergence of novel targeted migraine treatments more recently, specifically calcitonin gene-related peptide (CGRP) receptor antagonists (gepants), has reignited interest in this strategy, with encouraging results. This review summarises historical and emerging data in this area, supporting use of the premonitory phase as an opportunity to intervene as early as possible in migraine to prevent attack-related morbidity.

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干预偏头痛的前驱期,预防偏头痛:药物疗法的前景。
偏头痛是一种常见的脑部疾病,其特点是发作时头痛伴有感觉敏感,令人丧失能力。尽管人们对偏头痛的神经生物学及其对治疗发展的影响有了越来越多的了解,但仍需要为现有疗法无法满足的患者提供治疗选择。首批开发的用于急性偏头痛治疗的特效药物--5-羟色胺[5-HT1B/1D]受体激动剂(三苯氧胺)似乎需要头痛发作时才能产生疗效,而在头痛升级前的轻微疼痛期间进行早期治疗可改善短期和长期疗效。有些患者发现,在头痛开始但未升级的早期窗口期进行治疗很困难,偏头痛可能在睡眠中或凌晨发作,因此在疼痛发作后及时治疗具有挑战性。有血管疾病的患者和年龄较大的患者可能不适合使用曲坦类药物,而且可能对一部分患者无效。人们越来越认识到,头痛只是偏头痛发作的众多症状之一,对一些患者来说,头痛并不是最严重的致残症状。在许多患者中,无痛症状可在头痛发作前出现,并能可靠地发出即将发生头痛的警告。因此,有必要确定可在发作过程中尽早使用的治疗目标和药物,以便在头痛发作前就加以预防,并减轻头痛和与头痛无关的发作负担。早期使用多潘立酮、那拉曲普坦和双氢麦角胺进行的小型研究表明,这种方法可能是有用的;这些研究在方法上不如现代治疗研究严谨,样本量也较小,而且后来没有进行过重复研究。最近出现的新型偏头痛靶向治疗方法,特别是降钙素基因相关肽(CGRP)受体拮抗剂(gepants),重新点燃了人们对这一策略的兴趣,并取得了令人鼓舞的结果。本综述总结了这一领域的历史数据和新出现的数据,支持利用偏头痛的前驱期作为尽早干预的机会,以预防发作相关的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CNS drugs
CNS drugs 医学-精神病学
CiteScore
12.00
自引率
3.30%
发文量
82
审稿时长
6-12 weeks
期刊介绍: CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes: - Overviews of contentious or emerging issues. - Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses. - Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. - Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry. - Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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