早老素
PSEN1型
疾病
发病机制
医学
阿尔茨海默病
突变
载脂蛋白E
淀粉样蛋白(真菌学)
早发性阿尔茨海默病
痴呆
病理
退行性疾病
遗传学
生物
基因
作者
Joseph F. Arboleda‐Velásquez,Francisco Lopera,Michael O’Hare,Santiago Delgado‐Tirado,Claudia Mariño,Natalia Chmielewska,Kahira L. Saez‐Torres,Dhanesh Amarnani,Aaron P. Schultz,Reisa A. Sperling,David Leyton-Cifuentes,Kewei Chen,Ana Baena,David Aguillón,Silvia Ríos‐Romenets,Margarita Giraldo,Edmarie Guzmán‐Vélez,Daniel Norton,Enmanuelle Pardilla‐Delgado,Arabiye Artola
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2019-11-01
卷期号:25 (11): 1680-1683
被引量:431
标识
DOI:10.1038/s41591-019-0611-3
摘要
We identified a PSEN1 (presenilin 1) mutation carrier from the world’s largest autosomal dominant Alzheimer’s disease kindred, who did not develop mild cognitive impairment until her seventies, three decades after the expected age of clinical onset. The individual had two copies of the APOE3 Christchurch (R136S) mutation, unusually high brain amyloid levels and limited tau and neurodegenerative measurements. Our findings have implications for the role of APOE in the pathogenesis, treatment and prevention of Alzheimer’s disease. A unique case from the Colombian cohort of autosomal dominant Alzheimer’s disease is reported in which disease progression is substantially delayed despite unusually high amyloid plaque pathology, possibly related to a rare mutation in APOE3.
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