简要报告:在法国非洲-加勒比人群中,DAT1基因与快克可卡因使用障碍之间存在正相关

Nicolas Ramoz , Jerome Lacoste , Guillaume Davido , Sandrine Lamy , Nicolas Ballon , Louis Jehel , Florence Thibaut
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摘要

前言快克可卡因使用障碍是一种主要的公共卫生疾病,具有很强的遗传性。目的本研究旨在探讨多巴胺转运蛋白基因(DAT1/SLC6A3)与快克可卡因使用障碍(CCUD)之间的关系,以及可能与注意力缺陷多动障碍(ADHD)、冲动和感觉寻求有关。使用Barratt冲动量表、Wender Utah量表-25项和Zuckerman感觉寻求量表。用TaqMan方法对受试者的DNA进行基因分型。结果我们发现DAT基因的两个SNPs(rs6347和rs27048)与快克可卡因使用障碍有关,DAT基因的三个单倍型区之一(AT单倍型,由之前的两个SNPs定义)和CCUD的频率显著较低。结论DAT1 rs6347和rs27048多态性似乎与CCUD有关。这些多态性的风险效应似乎是针对快克使用者的,而不是由冲动或多动症驱动的。
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Brief report: A positive association between the DAT1 gene and crack cocaine use disorders in a French Afro-Caribbean population

Introduction

Crack cocaine use disorder (CCUD) is a major public health with a strong heritability component.

Objectives

This study was aimed to investigate the putative association between the dopamine transporter gene (DAT1/SLC6A3) and crack-cocaine use disorders (CCUD) as well as the possible involvement of attention-deficit hyperactivity disorder (ADHD), impulsivity and sensation-seeking.

Methods

Seventy-seven male subjects with CCUD were compared with 60 male control subjects of Afro-Caribbean origin. The Barratt Impulsivity Scale, the Wender Utah scale Scale-25 item and the Zuckerman Sensation-Seeking Scale were used. The subjects’ DNAs were genotyped by quantitative PCR (TaqMan method).

Results

We found an association with two SNPs (rs6347 and rs27048) of the DAT gene in crack-cocaine use disorder, and a significantly lower frequency of one of the three haplotype blocks of the DAT gene (AT haplotype, defined by the two previous SNPs) and CCUD.

Conclusion

DAT1 rs6347 and rs27048 polymorphisms seem to be associated with CCUD. The risk-effect of these polymorphisms appeared to be specific to individuals who are crack users rather than being driven by impulsivity or ADHD.

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