Characterizing Prodrome (Premonitory Phase) in Migraine: Results From the PRODROME Trial Screening Period.

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200359
Todd J Schwedt, Richard B Lipton, Peter J Goadsby, Chia-Chun Chiang, Brad C Klein, Cory Hussar, Chengcheng Liu, Sung Yun Yu, Michelle Finnegan, Joel M Trugman
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引用次数: 0

Abstract

Background and objective: Limited data are available describing the frequency, severity, and consistency of prodromal symptoms followed by headache. This analysis of the PRODROME trial screening period characterized prodromal symptoms in people with migraine, including the most common symptoms and their severity, and the frequency and consistency with which prodromal symptoms were followed by headache.

Methods: PRODROME was a multicenter, randomized, double-blind, placebo-controlled, crossover trial conducted in the United States that enrolled adults with 2-8 migraine attacks per month who stated they could identify prodromal symptoms that were reliably followed by a headache. The trial included a 60-day screening period designed to test the predictive validity of "qualifying prodrome events" before the onset of headache. Participants used an eDiary to report qualifying prodrome events, defined as prodromal symptoms whereby the participant was confident a headache would follow within 1-6 hours. This analysis evaluated common prodromal symptoms and their severity, time from prodrome onset to headache onset, and the percentage of participants who identified prodromal symptoms that were followed by a headache ≥75% of the time over the 60-day screening period.

Results: A total of 920 participants entered eDiary data, with a mean of 5.2 qualifying prodrome events during the 60-day screening period. A total of 4,802 qualifying prodrome events were recorded. The most common prodromal symptoms identified were sensitivity to light (57.2%; 2,748/4,802), fatigue (50.1%; 2,408/4,802), neck pain (41.9%; 2,013/4,802), sensitivity to sound (33.9%; 1,630/4,802), either difficulty thinking or concentrating (30.0%; 1,442/4,802), and dizziness (27.8%; 1,333/4,802). Of all qualifying prodrome events reported, 81.5% (3,913/4,802) were followed by headache of any intensity within 1-6 hours. For each participant, a mean of 84.4% of their qualifying prodrome events were followed by a headache within 1-6 hours, with 76.9% of participants identifying qualifying prodrome events that were followed by headache within 1-6 hours ≥75% of the time.

Discussion: Participants were able to identify migraine attacks in which prodromal symptoms were reliably followed by a headache within 1-6 hours. These findings suggest the potential for initiating treatment during the prodrome to prevent headache.

Trial registration information: ClinicalTrials.gov NCT04492020. Submitted: July 27, 2020; First patient enrolled: August 21, 2020. clinicaltrials.gov/study/NCT04492020.

偏头痛前驱症状(前驱期)的特征:PRODROME 试验筛选期的结果。
背景和目的:目前描述头痛前驱症状的频率、严重程度和一致性的数据有限。这项对 PRODROME 试验筛选期的分析描述了偏头痛患者前驱症状的特点,包括最常见的症状及其严重程度,以及前驱症状后出现头痛的频率和一致性:PRODROME是一项在美国进行的多中心、随机、双盲、安慰剂对照、交叉试验,招募了每月偏头痛发作2-8次的成人患者,这些患者表示他们能识别出前驱症状,并能可靠地随之出现头痛。试验包括一个为期 60 天的筛查期,旨在测试头痛发作前 "合格前驱症状事件 "的预测有效性。参与者使用电子日记报告合格的前驱症状事件,合格的前驱症状是指参与者确信在 1-6 小时内会出现头痛的前驱症状。这项分析评估了常见的前驱症状及其严重程度、从前驱症状出现到头痛发作的时间,以及在 60 天的筛查期间,发现前驱症状后头痛发生率≥ 75% 的参与者比例:共有 920 名参与者输入了电子日记数据,在 60 天筛查期间平均有 5.2 次符合条件的前驱症状事件。共记录了 4802 次合格的前驱症状事件。最常见的前驱症状是对光敏感(57.2%;2,748/4,802)、疲劳(50.1%;2,408/4,802)、颈部疼痛(41.9%;2,013/4,802)、对声音敏感(33.9%;1,630/4,802)、思考困难或注意力不集中(30.0%;1,442/4,802)以及头晕(27.8%;1,333/4,802)。在所有报告的合格前驱症状中,81.5%(3,913/4,802)在 1-6 小时内出现任何强度的头痛。每位参与者平均有84.4%的合格前驱症状在1-6小时内伴有头痛,76.9%的参与者在≥75%的情况下能识别出在1-6小时内伴有头痛的合格前驱症状:讨论:参与者能够识别前驱症状在1-6小时内出现头痛的偏头痛发作。这些研究结果表明,在前驱症状出现时开始治疗,有可能预防头痛的发生:试验注册信息:ClinicalTrials.gov NCT04492020。提交时间:2020 年 7 月 27 日;首例患者入组时间:2020 年 8 月 21 日:Clinicaltrials.gov/study/NCT04492020。
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
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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