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Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood
Relatively little is known about how genetic influences on alcohol abuse and dependence (AAD) change with age. We examined the change in influence of genetic and environmental factors which explain symptoms of AAD from adolescence into early adulthood. Symptoms of AAD were assessed using the four AA...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253297/ https://www.ncbi.nlm.nih.gov/pubmed/21818662 http://dx.doi.org/10.1007/s10519-011-9488-8 |
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author | van Beek, Jenny H. D. A. Kendler, Kenneth S. de Moor, Marleen H. M. Geels, Lot M. Bartels, Meike Vink, Jacqueline M. van den Berg, Stéphanie M. Willemsen, Gonneke Boomsma, Dorret I. |
author_facet | van Beek, Jenny H. D. A. Kendler, Kenneth S. de Moor, Marleen H. M. Geels, Lot M. Bartels, Meike Vink, Jacqueline M. van den Berg, Stéphanie M. Willemsen, Gonneke Boomsma, Dorret I. |
author_sort | van Beek, Jenny H. D. A. |
collection | PubMed |
description | Relatively little is known about how genetic influences on alcohol abuse and dependence (AAD) change with age. We examined the change in influence of genetic and environmental factors which explain symptoms of AAD from adolescence into early adulthood. Symptoms of AAD were assessed using the four AAD screening questions of the CAGE inventory. Data were obtained up to six times by self-report questionnaires for 8,398 twins from the Netherlands Twin Register aged between 15 and 32 years. Longitudinal genetic simplex modeling was performed with Mx. Results showed that shared environmental influences were present for age 15–17 (57%) and age 18–20 (18%). Unique environmental influences gained importance over time, contributing 15% of the variance at age 15–17 and 48% at age 30–32. At younger ages, unique environmental influences were largely age-specific, while at later ages, age-specific influences became less important. Genetic influences on AAD symptoms over age could be accounted for by one factor, with the relative influence of this factor differing across ages. Genetic influences increased from 28% at age 15–17 to 58% at age 21–23 and remained high in magnitude thereafter. These results are in line with a developmentally stable hypothesis that predicts that a single set of genetic risk factors acts on symptoms of AAD from adolescence into young adulthood. |
format | Online Article Text |
id | pubmed-3253297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-32532972012-01-20 Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood van Beek, Jenny H. D. A. Kendler, Kenneth S. de Moor, Marleen H. M. Geels, Lot M. Bartels, Meike Vink, Jacqueline M. van den Berg, Stéphanie M. Willemsen, Gonneke Boomsma, Dorret I. Behav Genet Original Research Relatively little is known about how genetic influences on alcohol abuse and dependence (AAD) change with age. We examined the change in influence of genetic and environmental factors which explain symptoms of AAD from adolescence into early adulthood. Symptoms of AAD were assessed using the four AAD screening questions of the CAGE inventory. Data were obtained up to six times by self-report questionnaires for 8,398 twins from the Netherlands Twin Register aged between 15 and 32 years. Longitudinal genetic simplex modeling was performed with Mx. Results showed that shared environmental influences were present for age 15–17 (57%) and age 18–20 (18%). Unique environmental influences gained importance over time, contributing 15% of the variance at age 15–17 and 48% at age 30–32. At younger ages, unique environmental influences were largely age-specific, while at later ages, age-specific influences became less important. Genetic influences on AAD symptoms over age could be accounted for by one factor, with the relative influence of this factor differing across ages. Genetic influences increased from 28% at age 15–17 to 58% at age 21–23 and remained high in magnitude thereafter. These results are in line with a developmentally stable hypothesis that predicts that a single set of genetic risk factors acts on symptoms of AAD from adolescence into young adulthood. Springer US 2011-08-05 2012 /pmc/articles/PMC3253297/ /pubmed/21818662 http://dx.doi.org/10.1007/s10519-011-9488-8 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Research van Beek, Jenny H. D. A. Kendler, Kenneth S. de Moor, Marleen H. M. Geels, Lot M. Bartels, Meike Vink, Jacqueline M. van den Berg, Stéphanie M. Willemsen, Gonneke Boomsma, Dorret I. Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood |
title | Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood |
title_full | Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood |
title_fullStr | Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood |
title_full_unstemmed | Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood |
title_short | Stable Genetic Effects on Symptoms of Alcohol Abuse and Dependence from Adolescence into Early Adulthood |
title_sort | stable genetic effects on symptoms of alcohol abuse and dependence from adolescence into early adulthood |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253297/ https://www.ncbi.nlm.nih.gov/pubmed/21818662 http://dx.doi.org/10.1007/s10519-011-9488-8 |
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