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Association of CHRNA5 Gene Variants with Crack Cocaine Addiction.
Aroche, Angelita P; Rovaris, Diego L; Grevet, Eugenio H; Stolf, Anderson R; Sanvicente-Vieira, Breno; Kessler, Felix H P; von Diemen, Lisia; Grassi-Oliveira, Rodrigo; Bau, Claiton H D; Schuch, Jaqueline B.
Afiliação
  • Aroche AP; Department of Genetics, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Rovaris DL; Instituto de Ciencias Biomedicas, Departamento de Fisiologia e Biofisica, Universidade de Sao Paulo, São Paulo, Brazil.
  • Grevet EH; Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Stolf AR; ADHD Outpatient Program, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
  • Sanvicente-Vieira B; Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Kessler FHP; ADHD Outpatient Program, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
  • von Diemen L; Center for Drug and Alcohol Research, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande Do Sul, Porto Alegre, Brazil.
  • Grassi-Oliveira R; Developmental Cognitive Neuroscience Lab, Biomedical Research Institute, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
  • Bau CHD; Center for Drug and Alcohol Research, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande Do Sul, Porto Alegre, Brazil.
  • Schuch JB; Center for Drug and Alcohol Research, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande Do Sul, Porto Alegre, Brazil.
Neuromolecular Med ; 22(3): 384-390, 2020 09.
Article em En | MEDLINE | ID: mdl-32152934
ABSTRACT
Genome-wide studies provide increasing evidence of association of genetic variants with different behaviors. However, there is a growing need for replication and subsequent characterization of specific findings. In this sense, the CHRNA5 gene has been associated with nicotine (with genome-wide significance), alcohol and cocaine addictions. So far, this gene has not been evaluated in smoked (crack) cocaine. We aimed to analyze the influence of CHRNA5 variants in crack addiction susceptibility and severity. The sample includes 300 crack-addicted patients and 769 non-addicted individuals. The CHRNA5 SNPs evaluated were rs588765, rs16969968, and rs514743. Homozygosity for rs16969968 and rs588765 major alleles was nominally associated with a risk to crack addiction (GG, P = 0.032; CC, P = 0.036, respectively). Haplotype analyses reveal significant associations (rs588765|rs16969968|rs514743 pglobal-corrected = 7.66 × 10-5) and suggest a substantial role for rs16969968. These findings corroborate previous reports in cocaine addiction-in line with the expected effects of cocaine in the cholinergic system-and in the opposite direction of significant GWAS findings for nicotine addiction susceptibility. These results are strengthened by the first report of an association of rs588765 with crack addiction and by the haplotype findings. In summary, our study highlights the relevance of the α5 subunit on crack cocaine addiction, replicating previous results relating CHRNA5 with the genetics and pathophysiology of addiction of different drugs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Nicotínicos / Cocaína Crack / Transtornos Relacionados ao Uso de Cocaína / Polimorfismo de Nucleotídeo Único / Proteínas do Tecido Nervoso Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Neuromolecular Med Assunto da revista: BIOLOGIA MOLECULAR / NEUROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Nicotínicos / Cocaína Crack / Transtornos Relacionados ao Uso de Cocaína / Polimorfismo de Nucleotídeo Único / Proteínas do Tecido Nervoso Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Neuromolecular Med Assunto da revista: BIOLOGIA MOLECULAR / NEUROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Brasil