A genetic association study of tobacco withdrawal endophenotypes in African Americans.


Journal

Experimental and clinical psychopharmacology
ISSN: 1936-2293
Titre abrégé: Exp Clin Psychopharmacol
Pays: United States
ID NLM: 9419066

Informations de publication

Date de publication:
Oct 2022
Historique:
pubmed: 20 7 2021
medline: 6 10 2022
entrez: 19 7 2021
Statut: ppublish

Résumé

Genome-wide association (GWA) genetic epidemiology research has identified several variants modestly associated with brief self-report smoking measures, predominately in European Americans. GWA research has not applied intensive laboratory-based measures of smoking endophenotypes in African Americans-a population with disproportionately low quit smoking rates and high tobacco-related disease risk. This genetic epidemiology study of non-Hispanic African Americans tested associations of 89 genetic variants identified in previous GWA research and exploratory GWAs with 24 laboratory-derived tobacco withdrawal endophenotypes. African American cigarette smokers (N = 528; ≥10 cig/day; 36.2% female) completed two counterbalanced visits following either 16-hr of tobacco deprivation or ad libitum smoking. At both visits, self-report and behavioral measures across six unique "sub-phenotype" domains within the tobacco withdrawal syndrome were assessed (Urge/Craving, Negative Affect, Low Positive Affect, Cognition, Hunger, and Motivation to Resume Smoking). Results of the candidate variant analysis found two significant small-magnitude associations. The rs11915747 alternate allele in the CAD2M gene region was associated with .09 larger deprivation-induced changes in reported impulsivity (0-4 scale). The rs2471711alternate allele in the AC097480.1/AC097480.2 gene region was associated with 0.26 lower deprivation-induced changes in confusion (0-4 scale). For both variants, associations were opposite in direction to previous research. Individual genetic variants may exert only weak influences on tobacco withdrawal in African Americans. Larger sample sizes of non-European ancestry individuals might be needed to investigate both known and novel loci that may be ancestry-specific. (PsycInfo Database Record (c) 2022 APA, all rights reserved).

Identifiants

pubmed: 34279980
pii: 2021-59937-001
doi: 10.1037/pha0000492
pmc: PMC8928755
mid: NIHMS1784753
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

673-681

Subventions

Organisme : NIDA NIH HHS
ID : K24 DA048160
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA180905
Pays : United States
Organisme : American Cancer Society
Organisme : National Science Foundation

Auteurs

Adam M Leventhal (AM)

Department of Preventive Medicine, Keck School of Medicine, University of Southern California.

David V Conti (DV)

Department of Psychology, University of Southern California.

Lara A Ray (LA)

Department of Psychology, University of California, Los Angeles.

Mariel S Bello (MS)

Department of Psychology, University of Southern California.

Junhan Cho (J)

Department of Preventive Medicine, Keck School of Medicine, University of Southern California.

Yi Zhang (Y)

Department of Preventive Medicine, Keck School of Medicine, University of Southern California.

Mollie S Pester (MS)

Department of Psychology, University of Miami.

Lucas Lebovitz (L)

Department of Psychiatry, Keck School of Medicine, University of Southern California.

Arif Budiarto (A)

Bioinformatics and Data Science Research Center, Bina Nusantara University.

Bharuno Mahesworo (B)

Bioinformatics and Data Science Research Center, Bina Nusantara University.

Bens Pardamean (B)

BioRealm LLC.

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Classifications MeSH