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跨越TTC12和ANKK1、两侧为DRD2和NCAM1基因座的单倍型,在两个不同的美国人群中与尼古丁依赖密切相关。

Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations.

作者信息

Gelernter Joel, Yu Yi, Weiss Roger, Brady Kathleen, Panhuysen Carolien, Yang Bao-Zhu, Kranzler Henry R, Farrer Lindsay

机构信息

Division of Human Genetics, Department of Psychiatry, Yale University School of Medicine, West Haven, CT 06516, USA.

出版信息

Hum Mol Genet. 2006 Dec 15;15(24):3498-507. doi: 10.1093/hmg/ddl426. Epub 2006 Nov 3.

Abstract

Nicotine dependence (ND) is a moderately heritable trait. We ascertained a set of 1615 subjects in 632 families [319 African-American (AA) and 313 European-American (EA)] based on affected sibling pairs with cocaine or opioid dependence. Subjects were interviewed with the Semi-Structured Assessment for Drug Dependence and Alcoholism (SSADDA). Previously, we identified a modest linkage peak (LOD score =1.97) for ND in the EA part of the sample on chromosome 11q23, a region that includes the NCAM1-TTC12-ANKK1-DRD2 gene cluster. DRD2 and NCAM1 are functional candidate genes for substance dependence; the TTC12 and ANKK1 loci are not well characterized. We genotyped a set of 43 single nucleotide polymorphisms (SNPs) spanning this region, and performed family-based association and haplotype analysis. There was relatively weak evidence for association of the flanking DRD2 and NCAM1 markers to ND, but very strong evidence of association of multiple SNPs at TTC12 and ANKK1 in both populations (minimal P=0.0007 in AAs and minimal P=0.00009 in EAs), and in the pooled sample, as well as strong evidence for highly significant association of a single haplotype spanning TTC12 and ANKK1 to ND in the pooled sample (P=0.0000001). We conclude that a risk locus for ND, important both in AAs and EAs, maps to a region that spans TTC12 and ANKK1. Functional studies of these loci are warranted. These results provide additional information useful in evaluating the many earlier discrepant findings regarding association of DRD2 with substance dependence.

摘要

尼古丁依赖(ND)是一种具有中度遗传性的特质。我们基于患有可卡因或阿片类药物依赖的患病同胞对,在632个家庭中确定了一组1615名受试者[319名非裔美国人(AA)和313名欧裔美国人(EA)]。受试者接受了药物依赖和酒精中毒半结构化评估(SSADDA)。此前,我们在样本的欧裔美国人部分的11号染色体q23区域发现了一个与尼古丁依赖相关的适度连锁峰(LOD分数 = 1.97),该区域包含NCAM1 - TTC12 - ANKK1 - DRD2基因簇。DRD2和NCAM1是物质依赖的功能性候选基因;TTC12和ANKK1基因座的特征尚不明确。我们对跨越该区域的一组43个单核苷酸多态性(SNP)进行了基因分型,并进行了基于家系的关联分析和单倍型分析。侧翼的DRD2和NCAM1标记与尼古丁依赖相关的证据相对较弱,但在两个群体中(非裔美国人中最小P = 0.0007,欧裔美国人中最小P = 0.00009)以及合并样本中,TTC12和ANKK1处多个SNP与尼古丁依赖相关的证据非常强,同时在合并样本中也有强有力的证据表明跨越TTC12和ANKK1的单个单倍型与尼古丁依赖高度显著相关(P = 0.0000001)。我们得出结论,一个对非裔美国人和欧裔美国人都很重要的尼古丁依赖风险基因座定位于跨越TTC12和ANKK1的区域。对这些基因座进行功能研究是有必要的。这些结果为评估许多早期关于DRD2与物质依赖关联的不一致发现提供了额外的有用信息。

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