We’re moving! Datasets in the NIAGADS database are being transitioned to the DSS database, more info coming soon.

Association of apolipoprotein E genotype and Alzheimer disease in African Americans.

TitleAssociation of apolipoprotein E genotype and Alzheimer disease in African Americans.
Publication TypeJournal Article
Year of Publication2006
AuthorsMurrell, JR, Price, B, Lane, KA, Baiyewu, O, Gureje, O, Ogunniyi, A, Unverzagt, FW, Smith-Gamble, V, Gao, S, Hendrie, HC, Hall, KS
JournalArch Neurol
Volume63
Issue3
Pagination431-4
Date Published2006 Mar
ISSN0003-9942
KeywordsAfrican Americans, Aged, Aged, 80 and over, Alzheimer Disease, Apolipoproteins E, Female, Genotype, Humans, Logistic Models, Male, Risk
Abstract

BACKGROUND: 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.

OBJECTIVE: To determine the effect of apolipoprotein E (APOE) genotype on the risk of AD in elderly African Americans.

DESIGN: Population-based longitudinal study of AD.

SETTING: Indianapolis, Ind.

PARTICIPANTS: African Americans 65 years and older.

MAIN OUTCOME MEASURES: APOE genotype and diagnosis of AD.

RESULTS: 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).

CONCLUSIONS: 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.

DOI10.1001/archneur.63.3.431
Alternate JournalArch. Neurol.
PubMed ID16533971
PubMed Central IDPMC3203415
Grant ListR01 AG009956 / AG / NIA NIH HHS / United States
R01 AG09956 / AG / NIA NIH HHS / United States