Recent Efforts to Dissect the Genetic Basis of Alcohol Use and Abuse.


Journal

Biological psychiatry
ISSN: 1873-2402
Titre abrégé: Biol Psychiatry
Pays: United States
ID NLM: 0213264

Informations de publication

Date de publication:
01 04 2020
Historique:
received: 21 05 2019
revised: 14 08 2019
accepted: 13 09 2019
pubmed: 18 11 2019
medline: 7 1 2021
entrez: 18 11 2019
Statut: ppublish

Résumé

Alcohol use disorder (AUD) is defined by several symptom criteria, which can be dissected further at the genetic level. Over the past several years, our understanding of the genetic factors influencing alcohol use and abuse has progressed tremendously; numerous loci have been implicated in different aspects of alcohol use. Previously known associations with alcohol-metabolizing enzymes (ADH1B, ALDH2) have been replicated definitively. In addition, novel associations with loci containing the genes KLB, GCKR, CRHR1, and CADM2 have been reported. Downstream analyses have leveraged these genetic findings to reveal important relationships between alcohol use behaviors and both physical and mental health. AUD and aspects of alcohol misuse have been shown to overlap strongly with psychiatric disorders, whereas aspects of alcohol consumption have shown stronger links to metabolism. These results demonstrate that the genetic architecture of alcohol consumption only partially overlaps with the genetics of clinically defined AUD. We discuss the limitations of using quantitative measures of alcohol use as proxy measures for AUD, and we outline how future studies will require careful phenotype harmonization to properly capture the genetic liability to AUD.

Identifiants

pubmed: 31733789
pii: S0006-3223(19)31711-1
doi: 10.1016/j.biopsych.2019.09.011
pmc: PMC7071963
mid: NIHMS1550121
pii:
doi:

Substances chimiques

Ethanol 3K9958V90M
ADH1B protein, human EC 1.1.1.1
Alcohol Dehydrogenase EC 1.1.1.1
ALDH2 protein, human EC 1.2.1.3
Aldehyde Dehydrogenase, Mitochondrial EC 1.2.1.3

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

609-618

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : NIDA NIH HHS
ID : P50 DA037844
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA026281
Pays : United States
Organisme : NIMH NIH HHS
ID : R25 MH081482
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

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Auteurs

Sandra Sanchez-Roige (S)

Department of Psychiatry, University of California San Diego, La Jolla, California. Electronic address: sanchezroige@ucsd.edu.

Abraham A Palmer (AA)

Department of Psychiatry, University of California San Diego, La Jolla, California; Institute for Genomic Medicine, University of California San Diego, La Jolla, California.

Toni-Kim Clarke (TK)

Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom.

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