Forecasting the prevalence of preclinical and clinical Alzheimer's disease in the United States

被引:311
作者
Brookmeyer, Ron [1 ]
Abdalla, Nada [1 ]
Kawas, Claudia H. [2 ,3 ,4 ]
Corrada, Maria M. [2 ,4 ,5 ]
机构
[1] Univ Calif Los Angeles, Dept Biostat, Los Angeles, CA USA
[2] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
[3] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA USA
[4] Univ Calif Irvine, Inst Memory Impairments & Neurol Disorders, Irvine, CA USA
[5] Univ Calif Irvine, Dept Epidemiol, Irvine, CA USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Forecast; Intervention; Prediction; Prevalence; Prevention; Statistics; MILD COGNITIVE IMPAIRMENT; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; NEURODEGENERATION; RECOMMENDATIONS; DEMENTIA; POPULATION; SURVIVAL; COHORT;
D O I
10.1016/j.jalz.2017.10.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: We forecast the prevalence of preclinical and clinical Alzheimer's disease (AD) and evaluated potential impacts of primary and secondary preventions in the United States. Methods: We used a multistate model incorporating biomarkers for preclinical AD with US population projections. Results: Approximately 6.08 million Americans had either clinical AD or mild cognitive impairment due to AD in 2017 and that will grow to 15.0 million by 2060. In 2017, 46.7 million Americans had preclinical AD (amyloidosis, neurodegeneration, or both), although many may not progress to clinical disease during their lifetimes. Primary and secondary preventions have differential impact on future disease burden. Discussion: Because large numbers of persons are living with preclinical AD, our results underscore the need for secondary preventions for persons with existing AD brain pathology who are likely to develop clinical disease during their lifetimes as well as primary preventions for persons without preclinical disease. (C) 2017 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:121 / 129
页数:9
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