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Identifying Genetic Variation for Alcohol Dependence

Researchers are using various strategies to identify the genes that may be associated with alcoholism. The initial efforts primarily relied on candidate gene and linkage studies; more recently, however, modern advances in genotyping have resulted in widespread use of genome-wide association studies...

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Detalles Bibliográficos
Autores principales: Agrawal, Arpana, Bierut, Laura J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute on Alcohol Abuse and Alcoholism 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662475/
https://www.ncbi.nlm.nih.gov/pubmed/23134043
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author Agrawal, Arpana
Bierut, Laura J.
author_facet Agrawal, Arpana
Bierut, Laura J.
author_sort Agrawal, Arpana
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description Researchers are using various strategies to identify the genes that may be associated with alcoholism. The initial efforts primarily relied on candidate gene and linkage studies; more recently, however, modern advances in genotyping have resulted in widespread use of genome-wide association studies for alcohol dependence. The key findings of the earlier studies were that variations (i.e., polymorphisms) in the DNA sequences of the genes encoding alcohol dehydrogenase 1B (i.e., the ADH1B gene), aldehyde dehydrogenase 2 (i.e., the ALDH2 gene), and other alcohol-metabolizing enzymes mediate the risk for alcoholism; moreover, these polymorphisms also have an impact on the risk of alcohol-related cancers, such as esophageal cancer. In addition, a gene encoding one of the receptors for the neurotransmitter γ-aminobutyric acid (GABA) known as GABRA2 seems to have a role in the development of alcohol dependence. Genome-wide association studies now offer a host of emerging opportunities, as well as challenges, for discovering the genetic etiology of alcohol dependence and for unveiling new treatment strategies.
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spelling pubmed-36624752013-05-23 Identifying Genetic Variation for Alcohol Dependence Agrawal, Arpana Bierut, Laura J. Alcohol Res Articles Researchers are using various strategies to identify the genes that may be associated with alcoholism. The initial efforts primarily relied on candidate gene and linkage studies; more recently, however, modern advances in genotyping have resulted in widespread use of genome-wide association studies for alcohol dependence. The key findings of the earlier studies were that variations (i.e., polymorphisms) in the DNA sequences of the genes encoding alcohol dehydrogenase 1B (i.e., the ADH1B gene), aldehyde dehydrogenase 2 (i.e., the ALDH2 gene), and other alcohol-metabolizing enzymes mediate the risk for alcoholism; moreover, these polymorphisms also have an impact on the risk of alcohol-related cancers, such as esophageal cancer. In addition, a gene encoding one of the receptors for the neurotransmitter γ-aminobutyric acid (GABA) known as GABRA2 seems to have a role in the development of alcohol dependence. Genome-wide association studies now offer a host of emerging opportunities, as well as challenges, for discovering the genetic etiology of alcohol dependence and for unveiling new treatment strategies. National Institute on Alcohol Abuse and Alcoholism 2012 /pmc/articles/PMC3662475/ /pubmed/23134043 Text en http://creativecommons.org/publicdomain/mark/1.0/ Unless otherwise noted in the text, all material appearing in this journal is in the public domain and may be reproduced without permission. Citation of the source is appreciated.
spellingShingle Articles
Agrawal, Arpana
Bierut, Laura J.
Identifying Genetic Variation for Alcohol Dependence
title Identifying Genetic Variation for Alcohol Dependence
title_full Identifying Genetic Variation for Alcohol Dependence
title_fullStr Identifying Genetic Variation for Alcohol Dependence
title_full_unstemmed Identifying Genetic Variation for Alcohol Dependence
title_short Identifying Genetic Variation for Alcohol Dependence
title_sort identifying genetic variation for alcohol dependence
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662475/
https://www.ncbi.nlm.nih.gov/pubmed/23134043
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