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

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Standard

Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration. / Nordestgaard, Liv Tybjærg; Christoffersen, Mette; Afzal, Shoaib; Nordestgaard, Børge Grønne; Tybjærg-Hansen, Anne; Frikke-Schmidt, Ruth.

I: European Journal of Epidemiology, Bind 38, Nr. 9, 2023, s. 985-994.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Nordestgaard, LT, Christoffersen, M, Afzal, S, Nordestgaard, BG, Tybjærg-Hansen, A & Frikke-Schmidt, R 2023, 'Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration', European Journal of Epidemiology, bind 38, nr. 9, s. 985-994. https://doi.org/10.1007/s10654-023-01021-4

APA

Nordestgaard, L. T., Christoffersen, M., Afzal, S., Nordestgaard, B. G., Tybjærg-Hansen, A., & Frikke-Schmidt, R. (2023). Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration. European Journal of Epidemiology, 38(9), 985-994. https://doi.org/10.1007/s10654-023-01021-4

Vancouver

Nordestgaard LT, Christoffersen M, Afzal S, Nordestgaard BG, Tybjærg-Hansen A, Frikke-Schmidt R. Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration. European Journal of Epidemiology. 2023;38(9):985-994. https://doi.org/10.1007/s10654-023-01021-4

Author

Nordestgaard, Liv Tybjærg ; Christoffersen, Mette ; Afzal, Shoaib ; Nordestgaard, Børge Grønne ; Tybjærg-Hansen, Anne ; Frikke-Schmidt, Ruth. / Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration. I: European Journal of Epidemiology. 2023 ; Bind 38, Nr. 9. s. 985-994.

Bibtex

@article{5c73775a5df748aeb80a3c6f7ef2d82c,
title = "Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration",
abstract = "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.",
keywords = "ATP-binding cassette transporter A1, Blindness, Cholesterol, Drusen, Genetics, High-density lipoprotein",
author = "Nordestgaard, {Liv Tybj{\ae}rg} and Mette Christoffersen and Shoaib Afzal and Nordestgaard, {B{\o}rge Gr{\o}nne} and Anne Tybj{\ae}rg-Hansen and Ruth Frikke-Schmidt",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2023",
doi = "10.1007/s10654-023-01021-4",
language = "English",
volume = "38",
pages = "985--994",
journal = "European Journal of Epidemiology",
issn = "0393-2990",
publisher = "Springer",
number = "9",

}

RIS

TY - JOUR

T1 - Genetic variants in the adenosine triphosphate-binding cassette transporter A1 and risk of age-related macular degeneration

AU - Nordestgaard, Liv Tybjærg

AU - Christoffersen, Mette

AU - Afzal, Shoaib

AU - Nordestgaard, Børge Grønne

AU - Tybjærg-Hansen, Anne

AU - Frikke-Schmidt, Ruth

N1 - Publisher Copyright: © 2023, The Author(s).

PY - 2023

Y1 - 2023

N2 - 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.

AB - 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.

KW - ATP-binding cassette transporter A1

KW - Blindness

KW - Cholesterol

KW - Drusen

KW - Genetics

KW - High-density lipoprotein

U2 - 10.1007/s10654-023-01021-4

DO - 10.1007/s10654-023-01021-4

M3 - Journal article

C2 - 37335386

AN - SCOPUS:85162255927

VL - 38

SP - 985

EP - 994

JO - European Journal of Epidemiology

JF - European Journal of Epidemiology

SN - 0393-2990

IS - 9

ER -

ID: 367088690