Proudnikov Dmitri, LaForge K Steven, Hofflich Heather, Levenstien Mark, Gordon Derek, Barral Sandra, Ott Jurg, Kreek Mary Jeanne
Laboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
Pharmacogenet Genomics. 2006 Jan;16(1):25-36. doi: 10.1097/01.fpc.0000182782.87932.d6.
5-Hydroxytryptamine (serotonin)-1B receptors (HTR1B) may play an important role in psychiatric disorders and drug and alcohol dependence. In this study we report on genotype, molecular haplotype and statistically estimated haplotype analyses of previously identified polymorphisms in positions -261T>G, -161A>T, 129C>T, 861G>C and 1180A>G of the HTR1B gene in ethnically diverse populations (African-Americans, Caucasians, Hispanics and Asians) including 235 former heroin addicts and 161 control subjects from New York City. The objectives were to test for an association of molecular and statistically estimated haplotypes and genotypes in HTR1B gene with heroin addiction and to compare results provided by molecular and statistically estimated haplotyping methods.
Genotype analysis was performed using a standard TaqMan protocol. Molecular haplotype analysis of the subset of polymorphisms consisting of -261T>G, -161A>T and 129C>T was performed using a protocol specially designed by our group, using fluorescent PCR. This is based on use of allele-specific primers complementary to flanking polymorphisms and a fluorescently labeled sequence-specific TaqMan probe set complementary to an internal polymorphism of the haplotype region. Every individual's statistically inferred haplotype pair agreed with the individual's haplotype pair determined by molecular haplotyping.
A point-wise significant association of haplotype pairs containing allele G at position 1180 with protective effect from heroin addiction in Caucasians was found. A point-wise nominally significant association of allele 1180G with a protective effect from heroin addiction was found in Caucasians. Statistically significant differences across four ethnic groups in control subjects for allelic frequencies of -261T>G and -161A>T were found.
5-羟色胺(血清素)-1B受体(HTR1B)可能在精神疾病以及药物和酒精依赖中发挥重要作用。在本研究中,我们报告了在包括235名纽约市前海洛因成瘾者和161名对照受试者在内的不同种族人群(非裔美国人、白种人、西班牙裔和亚洲人)中,对HTR1B基因中先前确定的-261T>G、-161A>T、129C>T、861G>C和1180A>G位置的多态性进行的基因型、分子单倍型和统计估计单倍型分析。目的是测试HTR1B基因中的分子和统计估计单倍型及基因型与海洛因成瘾之间的关联,并比较分子和统计估计单倍型分型方法提供的结果。
使用标准TaqMan方案进行基因型分析。对由-261T>G、-161A>T和129C>T组成的多态性子集进行分子单倍型分析,采用我们小组专门设计的方案,使用荧光PCR。这基于使用与侧翼多态性互补的等位基因特异性引物以及与单倍型区域内部多态性互补的荧光标记序列特异性TaqMan探针组。每个个体的统计推断单倍型对与通过分子单倍型分型确定的个体单倍型对一致。
在白种人中发现,包含1180位G等位基因的单倍型对与海洛因成瘾的保护作用存在逐点显著关联。在白种人中发现,1180G等位基因与海洛因成瘾的保护作用存在逐点名义上的显著关联。在对照受试者中,发现四个种族群体在-261T>G和-161A>T等位基因频率上存在统计学显著差异。