4.5 Article

Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies

Journal

HUMAN MUTATION
Volume 32, Issue 12, Pages 1407-1416

Publisher

WILEY-BLACKWELL
DOI: 10.1002/humu.21577

Keywords

age-related macular degeneration; AMD; apolipoprotein E; APOE; case-control association study

Funding

  1. Guide Dogs for the Blind Association UK [2008-5a, OR2006-02d]
  2. Medical Research Council [G0000067]
  3. Research and Development Office, Northern Ireland Health Personal Social Services [RRG 4.5 - GS]
  4. EVI-GENORET
  5. The Deutsche Forschungsgemeinschaft [WE1259/18-1, WE1259/19-1]
  6. Alcon Research Institute and the Ruth and Milton Steinbach Foundation New York
  7. Tufts University School of Medicine
  8. Tufts Medical Center
  9. Massachusetts Lions Eye Research Fund
  10. Research to Prevent Blindness USA
  11. Foundation Fighting Blindness
  12. Department of Health via National Institute for Health Research
  13. National Health & Medical Research Council of Australia Centre for Clinical Research Excellence [529923]
  14. Victorian Government
  15. Macular Disease Society
  16. T.F.C. Frost Charity
  17. British Council for the Prevention of Blindness
  18. MRC [G0601354]
  19. Estonian Ministry of Education and Science
  20. ESRC [ES/G007438/1] Funding Source: UKRI
  21. MRC [G0000067, MC_U127584475, G0601354] Funding Source: UKRI
  22. Grants-in-Aid for Scientific Research [22890007] Funding Source: KAKEN
  23. British Heart Foundation [RG/10/12/28456] Funding Source: researchfish
  24. Economic and Social Research Council [ES/G007438/1] Funding Source: researchfish
  25. Medical Research Council [MC_U127584475, G0700704B, G0601354, MC_PC_U127584475, G0000067] Funding Source: researchfish
  26. National Institute for Health Research [NF-SI-0507-10094] Funding Source: researchfish

Ask authors/readers for more resources

Age-related macular degeneration (AMD) is the most common cause of incurable visual impairment in high-income countries. Previous studies report inconsistent associations between AMD and apolipoprotein E (APOE), a lipid transport protein involved in low-density cholesterol modulation. Potential interaction between APOE and sex, and smoking status has been reported. We present a pooled analysis (n = 21,160) demonstrating associations between late AMD and APOe4 (odds ratio [OR] = 0.72 per haplotype; confidence interval [CI]: 0.650.74; P = 4.41 x 10-11) and APOe2 (OR = 1.83 for homozygote carriers; CI: 1.043.23; P = 0.04), following adjustment for age group and sex within each study and smoking status. No evidence of interaction between APOE and sex or smoking was found. Ever smokers had significant increased risk relative to never smokers for both neovascular (OR = 1.54; CI: 1.381.72; P = 2.8 x 10(-15)) and atrophic (OR = 1.38; CI: 1.181.61; P = 3.37 x 10(-5)) AMD but not early AMD (OR = 0.94; CI: 0.861.03; P = 0.16), implicating smoking as a major contributing factor to disease progression from early signs to the visually disabling late forms. Extended haplotype analysis incorporating rs405509 did not identify additional risks beyond e2 and e4 haplotypes. Our expanded analysis substantially improves our understanding of the association between the APOE locus and AMD. It further provides evidence supporting the role of cholesterol modulation, and low-density cholesterol specifically, in AMD disease etiology. 32:14071416, 2011. (C) 2011 Wiley Periodicals, Inc.

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