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Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood
Genetic effects on alcohol use can vary over time but are often examined using longitudinal models that predict a distal outcome at a single time point. The vast majority of these studies predominately examine effects using White, European American (EA) samples or examine the etiology of genetic var...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599703/ https://www.ncbi.nlm.nih.gov/pubmed/34789846 http://dx.doi.org/10.1038/s41598-021-01923-x |
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author | Elam, Kit K. Ha, Thao Neale, Zoe Aliev, Fazil Dick, Danielle Lemery-Chalfant, Kathryn |
author_facet | Elam, Kit K. Ha, Thao Neale, Zoe Aliev, Fazil Dick, Danielle Lemery-Chalfant, Kathryn |
author_sort | Elam, Kit K. |
collection | PubMed |
description | Genetic effects on alcohol use can vary over time but are often examined using longitudinal models that predict a distal outcome at a single time point. The vast majority of these studies predominately examine effects using White, European American (EA) samples or examine the etiology of genetic variants identified from EA samples in other racial/ethnic populations, leading to inconclusive findings about genetic effects on alcohol use. The current study examined how genetic influences on alcohol use varied by age across a 15 year period within a diverse ethnic/racial sample of adolescents. Using a multi-ethnic approach, polygenic risk scores were created for African American (AA, n = 192) and EA samples (n = 271) based on racially/ethnically aligned genome wide association studies. Age-varying associations between polygenic scores and alcohol use were examined from age 16 to 30 using time-varying effect models separately for AA and EA samples. Polygenic risk for alcohol use was found to be associated with alcohol use from age 22–27 in the AA sample and from age 24.50 to 29 in the EA sample. Results are discussed relative to the intersection of alcohol use and developmental genetic effects in diverse populations. |
format | Online Article Text |
id | pubmed-8599703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85997032021-11-19 Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood Elam, Kit K. Ha, Thao Neale, Zoe Aliev, Fazil Dick, Danielle Lemery-Chalfant, Kathryn Sci Rep Article Genetic effects on alcohol use can vary over time but are often examined using longitudinal models that predict a distal outcome at a single time point. The vast majority of these studies predominately examine effects using White, European American (EA) samples or examine the etiology of genetic variants identified from EA samples in other racial/ethnic populations, leading to inconclusive findings about genetic effects on alcohol use. The current study examined how genetic influences on alcohol use varied by age across a 15 year period within a diverse ethnic/racial sample of adolescents. Using a multi-ethnic approach, polygenic risk scores were created for African American (AA, n = 192) and EA samples (n = 271) based on racially/ethnically aligned genome wide association studies. Age-varying associations between polygenic scores and alcohol use were examined from age 16 to 30 using time-varying effect models separately for AA and EA samples. Polygenic risk for alcohol use was found to be associated with alcohol use from age 22–27 in the AA sample and from age 24.50 to 29 in the EA sample. Results are discussed relative to the intersection of alcohol use and developmental genetic effects in diverse populations. Nature Publishing Group UK 2021-11-17 /pmc/articles/PMC8599703/ /pubmed/34789846 http://dx.doi.org/10.1038/s41598-021-01923-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Elam, Kit K. Ha, Thao Neale, Zoe Aliev, Fazil Dick, Danielle Lemery-Chalfant, Kathryn Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood |
title | Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood |
title_full | Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood |
title_fullStr | Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood |
title_full_unstemmed | Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood |
title_short | Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood |
title_sort | age varying polygenic effects on alcohol use in african americans and european americans from adolescence to adulthood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599703/ https://www.ncbi.nlm.nih.gov/pubmed/34789846 http://dx.doi.org/10.1038/s41598-021-01923-x |
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