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多巴胺转运体基因多态性与戒烟之间的关联:一项荟萃分析。

Association between dopamine transporter genotypes and smoking cessation: a meta-analysis.

作者信息

Stapleton John A, Sutherland Gay, O'Gara Colin

机构信息

Tobacco Research Group, Department of Psychological Medicine, Kings College London, Institute of Psychiatry, London, UK.

出版信息

Addict Biol. 2007 Jun;12(2):221-6. doi: 10.1111/j.1369-1600.2007.00058.x.

Abstract

This review assessed the evidence of an association between genotypes of the dopamine transporter (DAT1, SLC6A3) 3' untranslated region (3'UTR) variable number of tandem repeats (VNTR) and smoking cessation. Five studies (seven cohorts) comprising 2155 subjects were included in the meta-analysis. All gave data on the number of smokers who had stopped smoking and the number still smoking for those with one or more variant 9-repeat alleles and other genotypes. Three studies (comprising five cohorts) were cross-sectional population surveys and two were smoking cessation treatment programs with follow-up. Four of the five studies (six of the seven cohorts) showed a trend in favor of cessation when the variant 9-repeat allele was present, although only one study showed a statistically significant effect. The pooled odds ratio in favor of a greater likelihood of cessation for the variant 9-repeat allele was 1.15 [95% confidence interval (CI) = 0.97-1.37]. In a more refined analysis where cohorts within studies were treated as separate samples and adjusted odds ratios were used, the overall pooled odds ratio in favor of cessation with the 9-repeat alleles was 1.20 (95% CI = 1.01-1.43). These results support the hypothesis that the DAT1 3'UTR VNTR polymorphism is associated with smoking cessation. One or more variant 9-repeat alleles relative to the more common 10-repeat allele confers a greater likelihood of cessation, indicative of lower dependence on tobacco. The effect was a 20% increase in the odds of cessation for those with a variant allele.

摘要

本综述评估了多巴胺转运体(DAT1,SLC6A3)3'非翻译区(3'UTR)可变数目串联重复序列(VNTR)基因型与戒烟之间关联的证据。荟萃分析纳入了五项研究(七个队列),共2155名受试者。所有研究均给出了携带一个或多个9重复等位基因变异体及其他基因型的吸烟者中已戒烟者数量和仍在吸烟者数量的数据。三项研究(包含五个队列)为横断面人群调查,两项为有随访的戒烟治疗项目。五项研究中的四项(七个队列中的六项)显示,当存在9重复等位基因变异体时,有戒烟的趋势,尽管只有一项研究显示出统计学显著效应。支持9重复等位基因变异体戒烟可能性更大的合并优势比为1.15[95%置信区间(CI)=0.97 - 1.37]。在一项更精细的分析中,将研究中的队列视为独立样本并使用调整后的优势比,支持9重复等位基因戒烟的总体合并优势比为1.20(95%CI = 1.01 - 1.43)。这些结果支持以下假设:DAT1 3'UTR VNTR多态性与戒烟有关。相对于更常见的10重复等位基因,一个或多个9重复等位基因变异体使戒烟的可能性更大,表明对烟草的依赖性更低。对于携带变异等位基因的人,戒烟几率增加了20%。

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