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Tytuł pozycji:

Epistatic effect of Ankyrin repeat and kinase domain containing 1 - Dopamine receptor D2 and catechol-o-methyltransferase single nucleotide polymorphisms on the risk for hazardous use of alcohol in Lithuanian population.

Tytuł:
Epistatic effect of Ankyrin repeat and kinase domain containing 1 - Dopamine receptor D2 and catechol-o-methyltransferase single nucleotide polymorphisms on the risk for hazardous use of alcohol in Lithuanian population.
Autorzy:
Kaminskaite M; Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania. Electronic address: .
Jokubka R; Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Janaviciute J; Department of Psychology, Vytautas Magnus University, Kaunas, Lithuania.
Lelyte I; Department of Psychology, Vytautas Magnus University, Kaunas, Lithuania.
Sinkariova L; Department of Psychology, Vytautas Magnus University, Kaunas, Lithuania.
Pranckeviciene A; Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Borutaite V; Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Bunevicius A; Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Źródło:
Gene [Gene] 2021 Jan 10; Vol. 765, pp. 145107. Date of Electronic Publication: 2020 Sep 02.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Amsterdam, Elsevier/North-Holland, 1976-
MeSH Terms:
Alcoholism/*genetics
Catechol O-Methyltransferase/*genetics
Protein Serine-Threonine Kinases/*genetics
Receptors, Dopamine D2/*genetics
Adult ; Alcoholism/epidemiology ; Alleles ; Ankyrin Repeat/genetics ; Case-Control Studies ; Female ; Gene Frequency/genetics ; Genetic Association Studies ; Genetic Predisposition to Disease/genetics ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium/genetics ; Lithuania/epidemiology ; Male ; Middle Aged ; Polymorphism, Single Nucleotide/genetics ; Protein Serine-Threonine Kinases/metabolism ; Receptors, Dopamine D2/metabolism ; Risk Factors
Contributed Indexing:
Keywords: ANKK1-DRD2; Alcohol use disorder; COMT; Hazardous use of alcohol; Impulsiveness
Substance Nomenclature:
0 (DRD2 protein, human)
0 (Receptors, Dopamine D2)
EC 2.1.1.6 (COMT protein, human)
EC 2.1.1.6 (Catechol O-Methyltransferase)
EC 2.7.11.1 (ANKK1 protein, human)
EC 2.7.11.1 (Protein Serine-Threonine Kinases)
Entry Date(s):
Date Created: 20200905 Date Completed: 20201216 Latest Revision: 20211204
Update Code:
20240104
DOI:
10.1016/j.gene.2020.145107
PMID:
32889058
Czasopismo naukowe
Aim: The Lithuanian population has outstanding rates of alcohol consumption and alcohol related mortality. Alteration of brain dopaminergic system play a role in the risk for addiction disorders. We evaluated the association of one single nucleotide polymorphism rs1800497 in the Ankyrin Repeat and Kinase Domain Containing 1 - Dopamine Receptor D2 complex (ANKK1-DRD2) and a catechol-o-methyltransferase (COMT) rs4680 single nucleotide polymorphism with the risk for alcohol use disorder and impulsiveness in Lithuanian population. Both genetic polymorphisms are known to alter brain dopaminergic activity, thus we also investigated the possible interaction effect of these polymorphisms.
Methods: The study included 329 participants recruited from the local community. Hazardous alcohol use was evaluated using the Alcohol Use Disorder Identification Test (AUDIT). Impulsiveness was measured using the Barratt Impulsiveness Scale - 11 (BIS-11). Between group differences of AUDIT and BIS-11 scores were examined stratified by genetic polymorphisms and their combinations. The independent effect of each polymorphism and their interaction for hazardous alcohol use were evaluated using adjusted logistic regression analyses.
Results: The ANKK1-DRD2 rs1800497 polymorphism was associated with total AUDIT score, but not with the hazardous use of alcohol, as indicated by the AUDIT test cut-off of 8. The COMT rs4680 GG genotype was associated with the hazardous use of alcohol (adjusted OR = 2.094, p = 0.029), but this association was not statistically significant after adjustment for multiple comparisons. Presence of both COMT rs4680 and ANKK1-DRD2 rs1800497 GGxCT/TT polymorphisms was associated with significantly increased risk for hazardous use of alcohol (adjusted OR = 5.016, p = 0.005). The COMT rs4680 and ANKK1-DRD2 rs1800497 genetic polymorphisms, and their combination were not associated with impulsiveness.
Conclusions: Our study demonstrated that the interaction of COMT rs4680 and ANKK1-DRD2 rs1800497 genetic polymorphisms is associated with a hazardous use of alcohol.
(Copyright © 2020 Elsevier B.V. All rights reserved.)

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