Complex interactions underlie racial disparity in the risk of developing Alzheimer's disease dementia

被引:28
作者
Xiong, Chengjie [1 ,2 ]
Luo, Jingqin [1 ,3 ,4 ]
Coble, Dean [1 ,2 ]
Agboola, Folasade [1 ,2 ]
Kukull, Walter [5 ,6 ]
Morris, John C. [2 ,7 ,8 ]
机构
[1] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Knight Alzheimer Dis Res Ctr, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Surg, Div Publ Hlth Sci, St Louis, MO 63110 USA
[4] Washington Univ Sch Med, Siteman Canc Ctr Biostat Core, St Louis, MO USA
[5] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[6] Univ Washington, Natl Alzheimers Coordinating Ctr, Seattle, WA 98195 USA
[7] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[8] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
关键词
competing risk survival model; interactions; racial disparity; risk of Alzheimer's disease; ENTORHINAL CORTEX; COGNITIVE DECLINE; PREVALENCE; PROGRESSION; BIOMARKERS; VERSION; MODEL; RACE; AD;
D O I
10.1002/alz.12060
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: We aim to determine racial disparities and their modifying factors in risk for Alzheimer's disease (AD) dementia among cognitively normal individuals 65 years or older. Methods: Longitudinal data from the National Alzheimer's Coordinating Center Uniform Data Set on 1229 African Americans (AAs) and 6679 whites were analyzed for the risk of AD using competing risk models with death as a competing event. Results: Major AD risk factors modified racial differences which, when statistically significant, occurred only with older age among APOE epsilon 4 negative individuals, but also with younger age among APOE epsilon 4 positive individuals. The racial differences favored AAs among individuals with body mass index (BMI) < 30, but whites among individuals with a high BMI (>= 30), and were additionally modified by sex, education, hypertension, and smoking status. Conclusions: The presence, direction, and relative magnitude of racial disparity for AD represent an interactive function of major AD and cerebrovascular risk factors.
引用
收藏
页码:589 / 597
页数:9
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