Department of Genetics, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Instituto de Ciencias Biomedicas, Departamento de Fisiologia e Biofisica, Universidade de Sao Paulo, São Paulo, Brazil.
Neuromolecular Med. 2020 Sep;22(3):384-390. doi: 10.1007/s12017-020-08596-1. Epub 2020 Mar 10.
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 p = 7.66 × 10) 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.
全基因组研究为不同行为的遗传变异与关联提供了越来越多的证据。然而,越来越需要对特定发现进行复制和后续表征。在这种意义上,CHRNA5 基因与尼古丁(具有全基因组意义)、酒精和可卡因成瘾有关。到目前为止,该基因尚未在吸食(可卡因)可卡因中进行评估。我们旨在分析 CHRNA5 变体对吸食可卡因成瘾易感性和严重程度的影响。该样本包括 300 名吸食可卡因成瘾患者和 769 名非成瘾个体。评估的 CHRNA5 SNPs 是 rs588765、rs16969968 和 rs514743。rs16969968 和 rs588765 主要等位基因的纯合性与吸食可卡因成瘾的风险呈名义相关(GG,P=0.032;CC,P=0.036)。单体型分析显示出显著的关联(rs588765|rs16969968|rs514743 p=7.66×10),并提示 rs16969968 起重要作用。这些发现与可卡因成瘾的先前报告一致-与胆碱能系统中可卡因的预期作用一致-与尼古丁成瘾易感性的重大 GWAS 发现的方向相反。这些结果得到了 rs588765 与吸食可卡因成瘾相关的首次报告和单体型发现的支持。总之,我们的研究强调了 α5 亚基在吸食可卡因成瘾中的相关性,复制了先前与 CHRNA5 相关的不同药物成瘾的遗传学和病理生理学的结果。