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Association of CHRNA5 Gene Variants with Crack Cocaine Addiction

Authors :
Angelita P. Aroche
Anderson Ravy Stolf
Claiton H.D. Bau
Jaqueline Bohrer Schuch
Lisia von Diemen
Diego L. Rovaris
Breno Sanvicente-Vieira
Felix Kessler
Eugenio H. Grevet
Rodrigo Grassi-Oliveira
Source :
NeuroMolecular Medicine. 22:384-390
Publication Year :
2020
Publisher :
Springer Science and Business Media LLC, 2020.

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.

Details

ISSN :
15591174 and 15351084
Volume :
22
Database :
OpenAIRE
Journal :
NeuroMolecular Medicine
Accession number :
edsair.doi.dedup.....23599aaa35da9f87a08312ec28b6c9f5
Full Text :
https://doi.org/10.1007/s12017-020-08596-1