Levran O, Londono D, O'Hara K, Randesi M, Rotrosen J, Casadonte P, Linzy S, Ott J, Adelson M, Kreek M J
The Laboratory of the Biology of Addictive Diseases, The Rockefeller University, New York, NY 10065, USA.
Genes Brain Behav. 2009 Jul;8(5):531-40. doi: 10.1111/j.1601-183X.2009.00501.x. Epub 2009 Jun 20.
Heroin addiction is a chronic complex disease with a substantial genetic contribution. This study was designed to identify gene variants associated with heroin addiction in African Americans. The emphasis was on genes involved in reward modulation, behavioral control, cognitive function, signal transduction and stress response. We have performed a case-control association analysis by screening with 1350 variants of 130 genes. The sample consisted of 202 former severe heroin addicts in methadone treatment and 167 healthy controls with no history of drug abuse. Single nucleotide polymorphism (SNP), haplotype and multi-SNP genotype pattern analyses were performed. Seventeen SNPs showed point-wise significant association with heroin addiction (nominal P< 0.01). These SNPs are from genes encoding several receptors: adrenergic (ADRA1A), arginine vasopressin (AVPR1A), cholinergic (CHRM2), dopamine (DRD1), GABA-A (GABRB3), glutamate (GRIN2A) and serotonin (HTR3A) as well as alcohol dehydrogenase (ADH7), glutamic acid decarboxylase (GAD1 and GAD2), the nucleoside transporter (SLC29A1) and diazepam-binding inhibitor (DBI). The most significant result of the analyses was obtained for the GRIN2A haplotype G-A-T (rs4587976-rs1071502-rs1366076) with protective effect (P(uncorrected) = 9.6E- 05, P(corrected) = 0.058). This study corroborates several reported associations with alcohol and drug addiction as well as other related disorders and extends the list of variants that may affect the development of heroin addiction. Further studies will be necessary to replicate these associations and to elucidate the roles of these variants in drug addiction vulnerability.
海洛因成瘾是一种具有显著遗传因素的慢性复杂疾病。本研究旨在识别非裔美国人中与海洛因成瘾相关的基因变异。重点关注参与奖赏调节、行为控制、认知功能、信号转导和应激反应的基因。我们通过对130个基因的1350个变异进行筛选,开展了病例对照关联分析。样本包括202名正在接受美沙酮治疗的 former severe海洛因成瘾者和167名无药物滥用史的健康对照。进行了单核苷酸多态性(SNP)、单倍型和多SNP基因型模式分析。17个SNP显示出与海洛因成瘾的逐点显著关联(名义P<0.01)。这些SNP来自编码几种受体的基因:肾上腺素能(ADRA1A)、精氨酸加压素(AVPR1A)、胆碱能(CHRM2)、多巴胺(DRD1)、GABA - A(GABRB3)、谷氨酸(GRIN2A)和5 - 羟色胺(HTR3A),以及乙醇脱氢酶(ADH7)、谷氨酸脱羧酶(GAD1和GAD2)、核苷转运体(SLC29A1)和地西泮结合抑制剂(DBI)。分析的最显著结果是GRIN2A单倍型G - A - T(rs4587976 - rs1071502 - rs1366076)具有保护作用(P(未校正)= 9.6E - 05,P(校正)= 0.058)。本研究证实了一些与酒精和药物成瘾以及其他相关疾病的报道关联,并扩展了可能影响海洛因成瘾发展的变异列表。需要进一步研究来重复这些关联,并阐明这些变异在药物成瘾易感性中的作用。