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Potential association of DRD2 and DAT1 genetic variation with heroin dependence.

机译:DRD2和DAT1遗传变异与海洛因依赖关系的潜在关联。

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The aim of our study was to investigate the potential association of dopamine receptor D2 gene (DRD2) TaqI RFLP A (rs1800497) and dopamine transporter gene (DAT) 3'untranslated region VNTR genetic variations with heroin addiction. Genotyping was performed using PCR-based techniques in 530 heroin abusers and 500 controls. Our results showed that DRD2 TaqI A1 allele carriers (genotypes A1A1 and A1A2) were prone to heroin abuse in models of dominance or co-dominance. We detected a 12 repeat allele and 6/6, 7/9, 9/11, 10/12 genotype in a Chinese/eastern Asian population for the first time. However, no significant differences in the DAT1 VNTR were found between the two groups in either genotypic or allelic distributions and there was no gene interaction between the two genetic loci.
机译:我们的研究目的是研究多巴胺受体D2基因(DRD2)TaqI RFLP A(rs1800497)和多巴胺转运蛋白基因(DAT)3'非翻译区VNTR遗传变异与海洛因成瘾的潜在关联。使用基于PCR的技术对530名海洛因滥用者和500名对照进行基因分型。我们的结果表明,在优势或共占模型中,DRD2 TaqI A1等位基因携带者(基因型A1A1和A1A2)易于滥用海洛因。我们首次在中国/东亚人群中检测到12个重复等位基因和6 / 6、7 / 9、9 / 11、10 / 12基因型。但是,两组在DAT1 VNTR的基因型或等位基因分布上均未发现显着差异,并且两个遗传基因座之间也没有基因相互作用。

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