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15q24 尼古丁受体亚基基因簇(CHRNA5-A3-B4)中的标志物可预测尼古丁成瘾的严重程度和对戒烟治疗的反应。

Markers in the 15q24 nicotinic receptor subunit gene cluster (CHRNA5-A3-B4) predict severity of nicotine addiction and response to smoking cessation therapy.

机构信息

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, California, 94305-5485, USA.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2011 Apr;156B(3):275-84. doi: 10.1002/ajmg.b.31155. Epub 2011 Jan 25.

DOI:10.1002/ajmg.b.31155
PMID:21268243
Abstract

Stopping smoking is difficult even with treatment. Many patients prescribed pharmacologic treatments for smoking cessation experience side effects or lack of efficacy. We performed a pharmacogenetic study of the efficacy and tolerability of bupropion and transdermal nicotine (TN), two treatments for smoking cessation. Samples were drawn from two studies. In the first study (Maintenance 1, MT1), 301 smokers received bupropion plus TN for 11 weeks, followed by 14 weeks of placebo or bupropion. In the second study (MT2), 276 smokers received bupropion and TN for 8 weeks. We focused on eight SNPs in the 15q24 region, which contains the genes for the nicotinic cholinergic receptor subunits CHRNA5, CHRNA3, and CHRNB4, and has previously been implicated in nicotine addiction and smoking cessation. Analyses of baseline smoking quantity (SQ) identified an association between SQ and both the functional CHRNA5 SNP rs16969968 (D398N) and the CHRNA3 SNP rs1051730 (Y215Y) in a combined cohort containing MT1 and MT2. An association between SQ and ethnicity was also identified in the combined cohort. Pharmacogenetic analysis showed a significant association between rs8192475 (R37H) in CHRNA3 and both higher craving after quitting and increased withdrawal symptoms over time in MT2. Two markers for point prevalence abstinence, CHRNA5 SNP rs680244 and CHRNB4 SNP rs12914008, were also identified in MT2, with the strongest findings at week 52. These results provide further support for the role of the CHRNA5/A3/B4 subunits in determining number of cigarettes smoked and response to smoking cessation therapy.

摘要

即使接受治疗,戒烟也很困难。许多接受戒烟药物治疗的患者会出现副作用或疗效不佳。我们对安非他酮和透皮尼古丁(TN)这两种戒烟药物的疗效和耐受性进行了遗传药理学研究。这些样本取自两项研究。在第一项研究(维持 1 期,MT1)中,301 名吸烟者接受了 11 周的安非他酮加 TN 治疗,随后接受了 14 周的安慰剂或安非他酮治疗。在第二项研究(MT2)中,276 名吸烟者接受了 8 周的安非他酮和 TN 治疗。我们集中研究了 15q24 区域的 8 个 SNP,该区域包含尼古丁胆碱能受体亚基 CHRNA5、CHRNA3 和 CHRNB4 的基因,先前与尼古丁成瘾和戒烟有关。对基线吸烟量(SQ)的分析发现,SQ 与包含 MT1 和 MT2 的联合队列中的功能性 CHRNA5 SNP rs16969968(D398N)和 CHRNA3 SNP rs1051730(Y215Y)均存在关联。联合队列中还发现 SQ 与种族存在关联。遗传药理学分析显示,CHRNA3 中的 rs8192475(R37H)与 MT2 中戒烟后更高的渴望和随时间推移增加的戒断症状之间存在显著关联。CHRNA5 SNP rs680244 和 CHRNB4 SNP rs12914008 这两个用于点患病率戒断的标记物也在 MT2 中被发现,在第 52 周时发现了最强的关联。这些结果进一步支持 CHRNA5/A3/B4 亚基在确定吸烟量和对戒烟治疗的反应中的作用。

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