载脂蛋白E
痴呆
医学
疾病
脑脊液
阶段(地层学)
内科学
持续时间(音乐)
基因型
发病年龄
肿瘤科
阿尔茨海默病
心理学
生物
遗传学
艺术
文学类
古生物学
基因
作者
Lisa Vermunt,Sietske A.M. Sikkes,Ardo van den Hout,Ron Handels,Isabelle Bos,Wiesje M. van der Flier,Silke Kern,Pierre‐Jean Ousset,Paul Maruff,Ingmar Skoog,Frans R.J. Verhey,Yvonne Freund‐Levi,Magda Tsolaki,Åsa K. Wallin,Marcel G. M. Olde Rikkert,Hilkka Soininen,L. Spiru,Henrik Zetterberg,Kaj Blennow,Philip Scheltens,Graciela Muñiz‐Terrera,Pieter Jelle Visser
标识
DOI:10.1016/j.jalz.2019.04.001
摘要
Abstract Introduction We estimated the age‐specific duration of the preclinical, prodromal, and dementia stages of Alzheimer's disease (AD) and the influence of sex, setting, apolipoprotein E ( APOE ) genotype, and cerebrospinal fluid tau on disease duration. Methods We performed multistate modeling in a combined sample of 6 cohorts (n = 3268) with death as the end stage and estimated the preclinical, prodromal, and dementia stage duration. Results The overall AD duration varied between 24 years (age 60) and 15 years (age 80). For individuals presenting with preclinical AD, age 70, the estimated preclinical AD duration was 10 years, prodromal AD 4 years, and dementia 6 years. Male sex, clinical setting, APOE ε4 allele carriership, and abnormal cerebrospinal fluid tau were associated with a shorter duration, and these effects depended on disease stage. Discussion Estimates of AD disease duration become more accurate if age, sex, setting, APOE , and cerebrospinal fluid tau are taken into account. This will be relevant for clinical practice and trial design.
科研通智能强力驱动
Strongly Powered by AbleSci AI