Cited by 108Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsGenetic Associations and Epidemiology

Association of Apolipoprotein E Genotype and Alzheimer Disease in African Americans

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Murrell, Jill R., Price, Brandon, Lane, Kathleen A., Baiyewu, Olusegun, Gureje, Oye, Ogunniyi, Adesola, Unverzagt, Frederick W., Smith-Gamble, Valerie +3 more·2006·Archives of Neurology

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.

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  • The association between APOEε4 and Alzheimer's disease is weaker among African-American and Hispanic individuals and nonexistent among Nigerian individuals.

    “the association between ε4 and disease is reported to be weaker among African-American and Hispanic individuals [58, 61, 62] and nonexistent among Nigerian individuals [63].”

    From Genetic architecture of Alzheimer's disease (2020) · cites this paper as [61]

  • The effect of APOEε4 on Alzheimer's disease risk differs across ethnicities.

    “the effect of APOEε4 has been reported to differ across ethnicities [58–61]”

    From Genetic architecture of Alzheimer's disease (2020) · cites this paper as [61]

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Authors
Murrell, J. R., Price, B., Lane, K. A., Baiyewu, O., Gureje, O., Ogunniyi, A., Unverzagt, F. W., Smith-Gamble, V., Gao, S., Hendrie, H. C., & Hall, K. S.
Affiliations
  • Indiana University Indianapolis (US)
  • Indiana University – Purdue University Indianapolis (US)
  • University of Ibadan (NG)
Venue
Archives of Neurology
Published
2006-03-01
Volume
63
Issue
3
Pages
431
ISSN
0003-9942 (ISSN-L)
OpenAlex
W2106392447
Cited by
108
References
4
Citations by year
2026: 2 · 2025: 6 · 2024: 5 · 2023: 5 · 2022: 13 · 2021: 7 · 2020: 2 · 2019: 4 · 2018: 1 · 2017: 2 · 2016: 12 · 2015: 4 · 2014: 4 · 2013: 8 · 2012: 2
FWCI
3.62
Type
journal article
Language
en
Open access
Locations
  • Archives of Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion)
Funders
National Institute on Aging (R01AG09956, R01AG009956)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
Keywords
Alzheimer's disease, apolipoprotein E, APOE ε4, APOE ε2, genetic risk factors, African Americans, older adults, dementia, genetic ancestry
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Apolipoproteins E, Black or African American, Female, Genotype, Humans, Male, Risk, Logistic Models

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