Levran O, Peles E, Randesi M, Li Y, Rotrosen J, Ott J, Adelson M, Kreek M J
The Laboratory of the Biology of Addictive Diseases, The Rockefeller University, New York, NY, USA.
Dr. Miriam and Sheldon G. Adelson Clinic for Drug Abuse Treatment and Research, Tel Aviv Elias Sourasky Medical Center, Tel Aviv, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Psychoneuroendocrinology. 2014 Jul;45:67-76. doi: 10.1016/j.psyneuen.2014.03.017. Epub 2014 Apr 6.
Stress is a critical risk factor affecting both the development of and the relapse to drug addictions. Drug addictions are caused by genetic, environmental and drug-induced factors. The objective of this hypothesis-driven association study was to determine if genetic variants in stress-related genes are associated with heroin addiction.
112 selected genetic variants in 26 stress-related genes were genotyped in 852 case subjects and 238 controls of predominantly European ancestry. The case subjects are former heroin addicts with a history of at least one year of daily multiple uses of heroin, treated at a methadone maintenance treatment program (MMTP). The two most promising SNPs were subsequently tested in an African-American sample comprising of 314 cases and 208 control individuals.
Nineteen single nucleotide polymorphisms (SNPs) in 9 genes (AVP, AVPR1A, CRHR1, CRHR2, FKBP5, GAL, GLRA1, NPY1R and NR3C2) showed nominally significant association with heroin addiction. The associations of two FKBP5 SNPs that are part of one haplotype block, rs1360780 (intron 2) and rs3800373 (the 3' untranslated region), remained significant after correction for multiple testing (Pcorrected=0.03; OR=2.35, Pcorrected=0.0018; OR=2.85, respectively). The two SNPs also showed nominally significant association (P<0.05) with heroin addiction in an independent African-American cohort. FKBP5 is a co-chaperone that regulates glucocorticoid sensitivity. These FKBP5 SNPs were previously associated with diverse affective disorders and showed functional differences in gene expression and stress response. This study also supports our and others' previous reports of association of the GAL SNP rs694066 and the AVPR1A SNPs rs11174811, rs1587097 and rs10784339 with heroin and general drug addiction, respectively.
This study suggests that variations in the FKBP5 gene contribute to the development of opiate addiction by modulating the stress response. These findings may enhance the understanding of the interaction between stress and heroin addiction.
压力是影响药物成瘾的发生和复发的关键风险因素。药物成瘾由遗传、环境和药物诱导因素引起。本项基于假设的关联研究旨在确定应激相关基因的遗传变异是否与海洛因成瘾有关。
对26个应激相关基因中的112个选定遗传变异进行基因分型,研究对象包括852例主要为欧洲血统的病例受试者和238例对照。病例受试者为曾吸食海洛因的成瘾者,有至少一年每日多次使用海洛因的历史,在美沙酮维持治疗项目(MMTP)接受治疗。随后,在一个由314例病例和208例对照个体组成的非裔美国人样本中对两个最有前景的单核苷酸多态性(SNP)进行了检测。
9个基因(AVP、AVPR1A、CRHR1、CRHR2、FKBP5、GAL、GLRA1、NPY1R和NR3C2)中的19个单核苷酸多态性(SNP)与海洛因成瘾呈名义上的显著关联。作为一个单倍型块一部分的两个FKBP5 SNP,rs1360780(内含子2)和rs3800373(3'非翻译区),在多重检验校正后仍具有显著相关性(校正P值 = 0.03;OR = 2.35,校正P值 = 0.0018;OR = 2.85)。这两个SNP在一个独立的非裔美国人队列中与海洛因成瘾也呈名义上的显著关联(P < 0.05)。FKBP5是一种调节糖皮质激素敏感性的辅助伴侣蛋白。这些FKBP5 SNP先前与多种情感障碍有关,并在基因表达和应激反应方面表现出功能差异。本研究还支持了我们和其他人先前分别报道的GAL SNP rs694066以及AVPR1A SNPs rs11174811、rs1587097和rs10784339与海洛因成瘾和一般药物成瘾的关联。
本研究表明,FKBP5基因的变异通过调节应激反应促成了阿片类药物成瘾的发生。这些发现可能会增进对压力与海洛因成瘾之间相互作用的理解。