Cited by 149Retinal Diseases and TreatmentsRetinal Imaging and AnalysisGenetic Associations and Epidemiology

A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy

Schmidt, Silke, Klaver, Caroline C. W., Saunders, Ann M., Postel, Eric A., De La Paz, Monica A., Agarwal, Anita, Small, Kent W., Udar, Nitin +15 more·2002·Ophthalmic Genetics

Abstract

Age-related maculopathy (ARM) is a multifactorial disorder known to have a substantial genetic component. The epsilon4 allele of the apolipoprotein E gene (APOE-4) has previously been reported to have a protective effect on ARM risk, while the APOE-2 allele may increase disease risk. This study combined four independent data sets (three US and one European) of Caucasian ARM patients and controls in order to obtain better statistical power to examine the role of APOE in ARM. APOE genotype and allele frequencies were compared for 617 ARM cases and 1260 controls, adjusting for age and sex differences between the two groups via multiple logistic regression. The protective effect of the APOE-4 allele on ARM risk was confirmed (age- and sex-adjusted odds ratio (OR) for APOE-4 carriers 0.54, 95% confidence interval (CI) 0.41-0.70, p < 0.0001). The effect of APOE-4 did not differ significantly between males and females and was observed consistently for both atrophic and neovascular ARM. Evidence for an increased risk of ARM due to the APOE-2 allele was found for men, but not for women (OR for men 1.54, 95% CI 0.97-2.45; OR for women 0.74, 95% CI 0.52-1.06, p = 0.01 for interaction of sex and APOE-2 carrier status). These data confirm that the APOE-4 allele, or an allele in linkage disequilibrium with it, reduces the risk of ARM. They also suggest that the effect of the APOE-2 allele may vary by gender, and that APOE-2 may confer an increased risk only to males.

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Crossref · 10.1076/opge.23.4.209.13883

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References 51 · Cited by 149

Authors
Schmidt, S., Klaver, C. C. W., Saunders, A. M., Postel, E. A., De La Paz, M. A., Agarwal, A., Small, K. W., Udar, N., Ong, J. M., Chalukya, M. V., Nesburn, A., Cristina Kenney, M., Domurath, R. M., Hogan, M., Mah, T. S., Conley, Y. P., Ferrell, R. E., Weeks, D. E., de Jong, P. T. V. M., van Duijn, C. M., Haines, J. L., Pericak-Vance, M. A., & Gorin, M. B.
Affiliations
  • Duke University (US)
  • Cedars-Sinai Medical Center (US)
  • University of Pittsburgh (US)
Venue
Ophthalmic Genetics
Published
2002-01
Volume
23
Issue
4
Pages
209-223
ISSN
  • 1381-6810 (ISSN-L)
  • 1744-5094
OpenAlex
W2024729125
Cited by
149
References
51
Citations by year
2026: 1 · 2025: 3 · 2022: 4 · 2021: 4 · 2020: 1 · 2019: 1 · 2018: 3 · 2017: 2 · 2016: 2 · 2015: 2 · 2014: 3 · 2013: 8 · 2012: 10
FWCI
8.36
Type
journal article
Language
en
Open access
closed
Locations
  • Ophthalmic Genetics (publishedVersion)
  • PubMed (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
  • KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
  • KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (submittedVersion)
Funders
  • National Institutes of Health (5r01ey010239-08)
  • National Institute on Aging (AG-11268, P60AG011268)
  • National Eye Institute (EY 09859, R01EY009859, EY10239, EY12118)
Topics
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal Imaging and Analysis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
Keywords
age-related maculopathy, apolipoprotein E, genetic susceptibility, sex differences, atrophic macular degeneration, neovascular age-related macular degeneration, linkage disequilibrium
MeSH terms
Aged, Aged, 80 and over, Apolipoproteins E, Female, Genotype, Humans, Macular Degeneration, Male, Middle Aged, Risk Factors, Case-Control Studies, Age Distribution, Genetic Predisposition to Disease, Apolipoprotein E3, Apolipoprotein E4, Apolipoprotein E2

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