Literature DB >> 29721579

GABAA receptor polymorphisms in alcohol use disorder in the GWAS era.

Mairi Koulentaki1,2, Elias Kouroumalis3.   

Abstract

Alcohol use disorder (AUD) is a chronic, relapsing, neuro-psychiatric illness of high prevalence and with a serious public health impact worldwide. It is complex and polygenic, with a heritability of about 50%, and influenced by environmental causal heterogeneity. Risk factors associated with its etiology have a genetic component. GABA (γ-aminobutyric acid) is a major inhibitory neurotransmitter in mammalian brain. GABAA receptors are believed to mediate some of the physiological and behavioral actions of alcohol. In this critical review, relevant genetic terms and type and methodology of the genetic studies are briefly explained. Postulated candidate genes that encode subunits of GABAA receptors, with all the reported SNPs, are presented. Genetic studies and meta-analyses examining polymorphisms of the GABAA receptor and their association with AUD predisposition are presented. The data are critically examined with reference to recent GWAS studies that failed to show relations between GABAA receptors and AUD. Restrictions and perspectives of the different findings are discussed.

Entities:  

Keywords:  Alcohol; Consumption; Dependence; GABA; GABA receptors; Linkage

Mesh:

Substances:

Year:  2018        PMID: 29721579     DOI: 10.1007/s00213-018-4918-4

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  195 in total

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3.  Bidirectional alterations of GABA(A) receptor subunit peptide levels in rat cortex during chronic ethanol consumption and withdrawal.

Authors:  L L Devaud; J M Fritschy; W Sieghart; A L Morrow
Journal:  J Neurochem       Date:  1997-07       Impact factor: 5.372

4.  Age of onset of drug use and its association with DSM-IV drug abuse and dependence: results from the National Longitudinal Alcohol Epidemiologic Survey.

Authors:  B F Grant; D A Dawson
Journal:  J Subst Abuse       Date:  1998

5.  Convergence of genome-wide association and candidate gene studies for alcoholism.

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Journal:  Alcohol Clin Exp Res       Date:  2012-09-14       Impact factor: 3.455

6.  An expanded evaluation of the relationship of four alleles to the level of response to alcohol and the alcoholism risk.

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7.  Complement factor H variant increases the risk of age-related macular degeneration.

Authors:  Jonathan L Haines; Michael A Hauser; Silke Schmidt; William K Scott; Lana M Olson; Paul Gallins; Kylee L Spencer; Shu Ying Kwan; Maher Noureddine; John R Gilbert; Nathalie Schnetz-Boutaud; Anita Agarwal; Eric A Postel; Margaret A Pericak-Vance
Journal:  Science       Date:  2005-03-10       Impact factor: 47.728

Review 8.  The role of GABAA receptors in mediating the effects of alcohol in the central nervous system.

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Journal:  Alcohol Alcohol       Date:  2016-04-26       Impact factor: 2.826

10.  Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo.

Authors:  Elena García-Martín; María I Ramos; José A Cornejo-García; Segismundo Galván; James R Perkins; Laura Rodríguez-Santos; Hortensia Alonso-Navarro; Félix J Jiménez-Jiménez; José A G Agúndez
Journal:  Front Cell Neurosci       Date:  2018-01-31       Impact factor: 5.505

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  4 in total

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2.  Female-specific decreases in alcohol binge-like drinking resulting from GABAA receptor delta-subunit knockdown in the VTA.

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Review 3.  Gut microbiota dysbiosis: The potential mechanisms by which alcohol disrupts gut and brain functions.

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Review 4.  Targeting prefrontal cortex GABAergic microcircuits for the treatment of alcohol use disorder.

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  4 in total

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