Frailty and Incident Dementia

被引:157
作者
Gray, Shelly L. [1 ]
Anderson, Melissa L. [2 ]
Hubbard, Rebecca A. [2 ]
LaCroix, Andrea [2 ,3 ]
Crane, Paul K. [4 ]
McCormick, Wayne [5 ]
Bowen, James D. [6 ]
McCurry, Susan M. [7 ]
Larson, Eric B. [2 ,4 ]
机构
[1] Univ Washington, Sch Pharm, Seattle, WA 98195 USA
[2] Grp Hlth Res Inst, Grp Hlth Cooperat, Seattle, WA USA
[3] Univ Washington, Sch Publ Hlth & Community Med, Dept Epidemiol, Seattle, WA 98195 USA
[4] Univ Washington, Div Gen Internal Med, Dept Med, Seattle, WA 98195 USA
[5] Univ Washington, Div Gerontol & Geriatr Med, Dept Med, Seattle, WA 98195 USA
[6] Swedish Neurosci Inst, Seattle, WA USA
[7] Univ Washington, Seattle, WA 98195 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2013年 / 68卷 / 09期
基金
美国国家卫生研究院;
关键词
Dementia; Alzheimers disease; Frailty; Epidemiology; ALZHEIMERS-DISEASE; COGNITIVE IMPAIRMENT; PHYSICAL FRAILTY; OLDER-ADULTS; HEALTH; OUTCOMES; RISK;
D O I
10.1093/gerona/glt013
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
We sought to examine whether frailty is associated with dementia, Alzheimers disease (AD), and non-AD dementia risk. This is a prospective population-based cohort derived from an integrated health maintenance organization. The sample consisted of 2,619 participants aged 65 and older without dementia at baseline followed from 1994 to 2010. Frailty was defined as having at least 3 of the following criteria: weakness (grip strength), slowness (walking speed), weight loss, low physical activity, and self-reported exhaustion. Follow-up occurred every 2 years to identify incident dementia, possible or probable AD, and non-AD dementia using standard research criteria. Covariates came from self-report and study measures. We used adjusted Cox proportional hazards models to examine the association between frailty and each outcome. Over a mean follow-up of 6.5 years, 521 participants developed dementia (of which 448 developed AD). In the model adjusted for age, sex, education, and race, the hazard ratio for frailty was 1.78 (95% confidence interval [CI] 1.322.40). In the fully adjusted models, the hazard ratio for frailty was 1.20 for all-cause dementia (95% CI 0.851.69), 1.08 for AD (95% CI 0.741.57), and 2.57 for non-AD dementia (95% CI 1.086.11). For all-cause dementia, we found an interaction between baseline cognitive score and frailty (p .02); hazard ratio for frailty was 1.78 for those with higher global cognition (95% CI 1.142.78) and 0.79 for those with lower global cognition (95% CI 0.501.26). Frailty was associated with dementia when adjusting only for demographic variables but not in the fully adjusted model. Frailty was associated with higher risk of developing non-AD dementia but not AD. Although frailty was not associated with all-cause dementia in the entire sample, an association did exist in participants with higher cognitive scores. Mechanisms underlying these associations remain to be elucidated.
引用
收藏
页码:1083 / 1090
页数:8
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