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糖尿病预防试验(DIAN)中15年的纵向基因、临床、认知、影像学和生化测量

15 Years of Longitudinal Genetic, Clinical, Cognitive, Imaging, and Biochemical Measures in DIAN.

作者信息

Daniels Alisha J, McDade Eric, Llibre-Guerra Jorge J, Xiong Chengjie, Perrin Richard J, Ibanez Laura, Supnet-Bell Charlene, Cruchaga Carlos, Goate Alison, Renton Alan E, Benzinger Tammie L S, Gordon Brian A, Hassenstab Jason, Karch Celeste, Popp Brent, Levey Allan, Morris John, Buckles Virginia, Allegri Ricardo F, Chrem Patricio, Berman Sarah B, Chhatwal Jasmeer P, Farlow Martin R, Fox Nick C, Day Gregory S, Ikeuchi Takeshi, Jucker Mathias, Lee Jae-Hong, Levin Johannes, Lopera Francisco, Takada Leonel, Sosa Ana Luisa, Martins Ralph, Mori Hiroshi, Noble James M, Salloway Stephen, Huey Edward, Rosa-Neto Pedro, Sánchez-Valle Raquel, Schofield Peter R, Roh Jee Hoon, Bateman Randall J

机构信息

Washington University School of Medicine, St Louis, St Louis, MO, USA.

Icahn School of Medicine at Mount Sinai, New York, NY USA.

出版信息

medRxiv. 2024 Aug 9:2024.08.08.24311689. doi: 10.1101/2024.08.08.24311689.

Abstract

This manuscript describes and summarizes the Dominantly Inherited Alzheimer Network Observational Study (DIAN Obs), highlighting the wealth of longitudinal data, samples, and results from this human cohort study of brain aging and a rare monogenic form of Alzheimer's disease (AD). DIAN Obs is an international collaborative longitudinal study initiated in 2008 with support from the National Institute on Aging (NIA), designed to obtain comprehensive and uniform data on brain biology and function in individuals at risk for autosomal dominant AD (ADAD). ADAD gene mutations in the amyloid protein precursor (), presenilin 1 (), or presenilin 2 () genes are deterministic causes of ADAD, with virtually full penetrance, and a predictable age at symptomatic onset. Data and specimens collected are derived from full clinical assessments, including neurologic and physical examinations, extensive cognitive batteries, structural and functional neuro-imaging, amyloid and tau pathological measures using positron emission tomography (PET), flurordeoxyglucose (FDG) PET, cerebrospinal fluid and blood collection (plasma, serum, and whole blood), extensive genetic and multi-omic analyses, and brain donation upon death. This comprehensive evaluation of the human nervous system is performed longitudinally in both mutation carriers and family non-carriers, providing one of the deepest and broadest evaluations of the human brain across decades and through AD progression. These extensive data sets and samples are available for researchers to address scientific questions on the human brain, aging, and AD.

摘要

本手稿描述并总结了显性遗传阿尔茨海默病网络观察性研究(DIAN Obs),重点介绍了这项关于大脑衰老和一种罕见的单基因形式阿尔茨海默病(AD)的人类队列研究中丰富的纵向数据、样本和结果。DIAN Obs是一项于2008年在美国国立衰老研究所(NIA)支持下启动的国际合作纵向研究,旨在获取常染色体显性AD(ADAD)风险个体大脑生物学和功能的全面且统一的数据。淀粉样蛋白前体()、早老素1()或早老素2()基因中的ADAD基因突变是ADAD的确定性病因,几乎具有完全的外显率,且症状出现的年龄可预测。所收集的数据和标本源自全面的临床评估,包括神经和体格检查、广泛的认知测试、结构和功能神经影像学、使用正电子发射断层扫描(PET)的淀粉样蛋白和tau病理测量、氟脱氧葡萄糖(FDG)PET、脑脊液和血液采集(血浆、血清和全血)、广泛的基因和多组学分析,以及死后大脑捐赠。这种对人类神经系统的全面评估在突变携带者和家族非携带者中进行纵向研究,提供了数十年来对人类大脑以及AD进展的最深入和最广泛的评估之一。这些广泛的数据集和样本可供研究人员解决有关人类大脑、衰老和AD的科学问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d4/11326320/12f24947bb52/nihpp-2024.08.08.24311689v1-f0044.jpg

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