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纵向早发性阿尔茨海默病研究(LEADS):框架与方法。

The Longitudinal Early-onset Alzheimer's Disease Study (LEADS): Framework and methodology.

机构信息

Department of Neurology, Indiana University School of Medicine, Indianapolis, Indiana, USA.

Department of Radiology and Imaging Sciences, Center for Neuroimaging, Indiana University School of Medicine Indianapolis, Indianapolis, Indiana, USA.

出版信息

Alzheimers Dement. 2021 Dec;17(12):2043-2055. doi: 10.1002/alz.12350. Epub 2021 May 21.

Abstract

Patients with early-onset Alzheimer's disease (EOAD) are commonly excluded from large-scale observational and therapeutic studies due to their young age, atypical presentation, or absence of pathogenic mutations. The goals of the Longitudinal EOAD Study (LEADS) are to (1) define the clinical, imaging, and fluid biomarker characteristics of EOAD; (2) develop sensitive cognitive and biomarker measures for future clinical and research use; and (3) establish a trial-ready network. LEADS will follow 400 amyloid beta (Aβ)-positive EOAD, 200 Aβ-negative EOnonAD that meet National Institute on Aging-Alzheimer's Association (NIA-AA) criteria for mild cognitive impairment (MCI) or AD dementia, and 100 age-matched controls. Participants will undergo clinical and cognitive assessments, magnetic resonance imaging (MRI), [ F]Florbetaben and [ F]Flortaucipir positron emission tomography (PET), lumbar puncture, and blood draw for DNA, RNA, plasma, serum and peripheral blood mononuclear cells, and post-mortem assessment. To develop more effective AD treatments, scientists need to understand the genetic, biological, and clinical processes involved in EOAD. LEADS will develop a public resource that will enable future planning and implementation of EOAD clinical trials.

摘要

早发性阿尔茨海默病(EOAD)患者由于年龄较小、表现不典型或缺乏致病性突变,通常被排除在大规模观察性和治疗性研究之外。纵向早发性阿尔茨海默病研究(LEADS)的目标是:(1)定义 EOAD 的临床、影像和液生物标志物特征;(2)开发用于未来临床和研究的敏感认知和生物标志物测量方法;(3)建立一个准备好进行试验的网络。LEADS 将跟踪 400 名淀粉样蛋白-β(Aβ)阳性的 EOAD 患者、200 名 Aβ 阴性的 EOnonAD 患者,这些患者符合国家老龄化协会-阿尔茨海默病协会(NIA-AA)轻度认知障碍(MCI)或 AD 痴呆的标准,以及 100 名年龄匹配的对照组。参与者将接受临床和认知评估、磁共振成像(MRI)、[ F]Florbetaben 和 [ F]Flortaucipir 正电子发射断层扫描(PET)、腰椎穿刺和血液抽取,用于 DNA、RNA、血浆、血清和外周血单核细胞,以及死后评估。为了开发更有效的 AD 治疗方法,科学家们需要了解 EOAD 中涉及的遗传、生物学和临床过程。LEADS 将开发一个公共资源,使未来能够规划和实施 EOAD 临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb48/9541332/7f58117a0ead/ALZ-17-2043-g002.jpg

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