Murrell Jill R, Price Brandon, Lane Kathleen A, Baiyewu Olusegun, Gureje Oye, Ogunniyi Adesola, Unverzagt Frederick W, Smith-Gamble Valerie, Gao Sujuan, Hendrie Hugh C, Hall Kathleen S
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, USA.
Arch Neurol. 2006 Mar;63(3):431-4. doi: 10.1001/archneur.63.3.431.
Alzheimer disease (AD) is the most frequent cause of dementia. Even though the incidence of AD in the African American population is similar to or higher than that in persons of European descent, AD in African Americans is understudied. Identification of genetic risk factors in African Americans is essential for understanding the etiology of AD.
To determine the effect of apolipoprotein E (APOE) genotype on the risk of AD in elderly African Americans.
Population-based longitudinal study of AD.
Indianapolis, Ind.
African Americans 65 years and older.
APOE genotype and diagnosis of AD.
The APOE genotype was determined in 1822 samples. Of these, 690 were clinically evaluated: 318 were normal, and 162 had a diagnosis of AD. The presence of APOE epsilon4 was significantly associated with increased risk of AD (epsilon3/epsilon4: OR, 2.32; 95% confidence interval [CI], 1.41-3.82; and epsilon4/epsilon4: OR, 7.19; 95% CI, 3.00-17.29, compared with the epsilon3/epsilon3 genotype). There was also a significant protective effect with APOE epsilon2 (epsilon2/epsilon2 and epsilon2/epsilon3: OR, 0.42; 95% CI, 0.20-0.89).
These findings are in marked contrast to the lack of association between APOE and AD in the Ibadan, Nigeria, sample of this project. These results suggest that other genetic factors and different environmental influences may play a role in the risk for AD in individuals of African ancestry.
阿尔茨海默病(AD)是痴呆最常见的病因。尽管非裔美国人中AD的发病率与欧洲裔人群相似或更高,但对非裔美国人AD的研究却很少。确定非裔美国人的遗传风险因素对于理解AD的病因至关重要。
确定载脂蛋白E(APOE)基因型对老年非裔美国人患AD风险的影响。
基于人群的AD纵向研究。
印第安纳州印第安纳波利斯。
65岁及以上的非裔美国人。
APOE基因型和AD诊断。
在1822份样本中确定了APOE基因型。其中,690份接受了临床评估:318份正常,162份被诊断为AD。APOE ε4的存在与AD风险增加显著相关(ε3/ε4:比值比[OR],2.32;95%置信区间[CI],1.41 - 3.82;ε4/ε4:OR,7.19;95%CI,3.00 - 17.29,与ε3/ε3基因型相比)。APOE ε2也有显著的保护作用(ε2/ε2和ε2/ε3:OR,0.42;95%CI,0.20 - 0.89)。
这些发现与本项目在尼日利亚伊巴丹样本中APOE与AD缺乏关联形成鲜明对比。这些结果表明,其他遗传因素和不同的环境影响可能在非洲裔个体患AD的风险中起作用。