Novel insights into the common heritable liability to addiction: a multivariate genome-wide association study
Détails
ID Serval
serval:BIB_F87F67D0514E
Type
Autre: (aucun autre type ne convient)
Collection
Publications
Institution
Titre
Novel insights into the common heritable liability to addiction: a multivariate genome-wide association study
Date de publication
2021
Langue
anglais
Notes
L2015874212
2021-12-28
2021-12-28
Résumé
Addiction to nicotine, alcohol and cannabis commonly co-occurs, which is thought to partly stem from a common heritable liability. To elucidate its genetic architecture, we modelled the common liability to addiction, inferred from genetic correlations among six measures of dependence and frequency of use of nicotine, alcohol and cannabis. Forty-two genetic variants were identified in the multivariate genome-wide association study on the common liability to addiction, of which 67% were novel and not associated with the six phenotypes. Mapped genes highlighted the role of dopamine (e.g., dopamine D2 gene), and showed enrichment for several components of the central nervous systems (e.g., mesocorticolimbic brain regions) and molecular pathways (dopaminergic, glutamatergic, GABAergic) that are thought to modulate drug reinforcement. Genetic correlations with other traits were most prominent for reward-related behaviours (e.g., risk-taking, cocaine and heroin use) and mood (e.g., depression, insomnia). These genome-wide results triangulate and expand previous preclinical and human studies focusing on the neurobiological substrates of addiction, and help to elucidate the common genetic architecture underlying addiction.
Mots-clé
addiction, alcohol consumption, brain region, genetic correlation, genetic variability, genome-wide association study, high risk behavior, human, insomnia, mood, phenotype, preclinical study, reinforcement (psychology), reward, alcohol, cannabis, cocaine, diamorphine, dopamine, nicotine
Site de l'éditeur
Création de la notice
14/01/2022 13:45
Dernière modification de la notice
21/01/2022 6:36