Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration

• Published in: European journal of epidemiology 2023-09, Vol.38 (9), p.985-994
• Main Authors: Nordestgaard, Liv Tybjærg, Christoffersen, Mette, Afzal, Shoaib, Nordestgaard, Børge Grønne, Tybjærg-Hansen, Anne, Frikke-Schmidt, Ruth
• Format: Article
• Language: English
• Subjects: ABCA1 protein; Adenosine triphosphate; Age related diseases; Alleles; Amino acids; ATP; ATP-binding protein; Cardiology; Cholesterol; Epidemiology; Eye diseases; Gene frequency; Genetic diversity; Genetic variance; High density lipoprotein; Infectious Diseases; Macular degeneration; Medicine; Medicine & Public Health; Oncology; Ophthalmic Epidemiology; Pathogenesis; Population studies; Public Health; Risk
• ISSN: 0393-2990; 1573-7284; 1573-7284
• DOI: 10.1007/s10654-023-01021-4

Genetic variants in ABCA1 are associated with higher concentrations of high-density lipoprotein (HDL) cholesterol. Higher HDL cholesterol concentrations are observationally and genetically associated with higher risk of age-related macular degeneration (AMD). However, whether amino acid-changing genetic variants in ABCA1 associated with high HDL cholesterol concentrations confer a higher risk of AMD in the general population is currently unknown. We tested this hypothesis. The study included 80,972 individuals (1,370 AMD cases) from the Copenhagen General Population Study (CGPS) and 9,584 individuals (142 AMD cases) from the Copenhagen City Heart Study (CCHS) with 10 to 18 years of follow-up. We created an HDL cholesterol weighted allele score based on amino acid-changing ABCA1 variants with a minor allele frequency above 0.001 and divided it into tertiles. The study included 55% women. Mean age was 58 years. The ABCA1 allele score for the third versus the first tertile was associated with HRs (95% confidence intervals (CIs)) of 1.30 (1.14–1.49) for all-cause AMD, 1.26 (1.06–1.50) for nonneovascular AMD, and 1.31 (1.12–1.53) for neovascular AMD in a multivariable adjusted model. On a continuous scale, higher concentrations of genetically determined HDL cholesterol were associated with higher risk of all-cause AMD, nonneovascular AMD, and neovascular AMD in an age- and sex adjusted model and in a multivariable adjusted model. In conclusion, amino acid-changing genetic variants in ABCA1 associated with higher HDL cholesterol concentrations were also associated with higher risk of AMD, suggesting a role for ABCA1 in AMD pathogenesis.