迟发性不明原因癫痫是认知障碍和痴呆的危险因素:一项多中心前瞻性纵向观察研究(ELUCID)的方案。

Alice D Lam, Emily L Johnson, Rani A Sarkis, Leah J Blank, Tyler E Gaston, Mouhsin M Shafi, Rodrigo Zepeda, Kyle R Pellerin, Nathalie Jette, Douglas N Greve, Lori B Chibnik, Rebecca E Amariglio, Gad A Marshall, M Brandon Westover
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引用次数: 0

摘要

背景:迟发性不明原因癫痫(Late-onset explanatory epilepsy, LoUE)定义为55岁以后无明显病因的癫痫发作,是痴呆的重要危险因素。研究表明,10-25%的LoUE患者在首次癫痫发作后的三至四年内发展为痴呆症。然而,从LoUE到痴呆的潜在机制仍然知之甚少。lucid研究的目的是确定与lue认知能力下降和痴呆发展相关的危险因素,并开发工具来识别这些结果的高风险患者,从而为该人群的痴呆预防策略奠定基础。方法和分析:ELUCID是一项多中心前瞻性纵向观察研究,将在美国7个医疗中心招募600名55岁及以上的lue患者。参与者接受基线评估,包括详细的临床病史、认知测试、脑MRI、夜间头皮脑电图和血液生物标志物。参与者将每隔6个月随访一次,记录认知和神经系统的变化,主要关注的结果是轻度认知障碍和/或痴呆的发展。本研究旨在基于生物标志物、认知轨迹和影像学特征建立LoUE疾病亚型,并开发一种风险分层工具,用于预测LoUE患者认知能力下降和痴呆的风险。伦理和传播:ELUCID已获得IRB批准(# 2023P001566, 2023年8月),马萨诸塞州布里格姆将军IRB作为唯一的IRB记录。所有去识别的研究数据将在研究完成后公开提供。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late-onset unexplained epilepsy as a risk factor for cognitive impairment and dementia: Protocol for a multi-center prospective longitudinal observational study (ELUCID).

Background: Late-onset unexplained epilepsy (LoUE), defined as epilepsy onset after age 55 without an obvious cause, is an important risk factor for dementia. Studies have shown that 10-25% of individuals with LoUE develop dementia within three to four years following their first seizure. However, the mechanisms underlying progression from LoUE to dementia remain poorly understood. The goals of the ELUCID study are to identify risk factors associated with development of cognitive decline and dementia in LoUE, and to develop tools to identify patients at high risk for these outcomes and thereby establish a foundation for dementia prevention strategies in this population.

Methods and analysis: ELUCID is a multi-center prospective longitudinal observational study that will enroll 600 participants aged 55 or older with LoUE across seven U.S. medical centers. Participants undergo a baseline evaluation that includes a detailed clinical history, cognitive testing, brain MRI, overnight scalp EEG, and blood biomarkers. Participants will be followed at six-month intervals to record cognitive and neurological changes, with the primary outcomes of interest being development of mild cognitive impairment and/or dementia. This study aims to establish LoUE disease subtypes based on biomarkers, cognitive trajectories, and imaging features, and to develop a risk stratification tool for predicting risk for cognitive decline and dementia in patients presenting with LoUE.

Ethics and dissemination: ELUCID has obtained IRB approval (# 2023P001566, August 2023), with the MassGeneral Brigham IRB serving as the single IRB of record. All de-identified study data will be made publicly available on completion of the study.

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