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本文引用的文献

1
Genetic association studies of methamphetamine use disorders: A systematic review and synthesis.甲基苯丙胺使用障碍的遗传关联研究:系统评价和综合分析。
Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1025-49. doi: 10.1002/ajmg.b.30936.
2
The prevalence of methamphetamine and amphetamine abuse in North America: a review of the indicators, 1992-2007.北美甲基苯丙胺和苯丙胺滥用的流行情况:1992 - 2007年指标综述
Drug Alcohol Rev. 2008 May;27(3):229-35. doi: 10.1080/09595230801919460.
3
Genome-wide association for methamphetamine dependence: convergent results from 2 samples.甲基苯丙胺依赖的全基因组关联研究:来自两个样本的一致结果。
Arch Gen Psychiatry. 2008 Mar;65(3):345-55. doi: 10.1001/archpsyc.65.3.345.
4
Possible association of beta-arrestin 2 gene with methamphetamine use disorder, but not schizophrenia.β-抑制蛋白2基因可能与甲基苯丙胺使用障碍有关,但与精神分裂症无关。
Genes Brain Behav. 2007 Feb;6(1):107-12. doi: 10.1111/j.1601-183X.2006.00237.x.
5
The need for speed: an update on methamphetamine addiction.对速度的需求:甲基苯丙胺成瘾的最新情况
J Psychiatry Neurosci. 2006 Sep;31(5):301-13.
6
Association between two mu-opioid receptor gene (OPRM1) haplotype blocks and drug or alcohol dependence.两种μ-阿片受体基因(OPRM1)单倍型模块与药物或酒精依赖之间的关联。
Hum Mol Genet. 2006 Mar 15;15(6):807-19. doi: 10.1093/hmg/ddl024. Epub 2006 Feb 13.
7
A haplotype map of the human genome.人类基因组单倍型图谱。
Nature. 2005 Oct 27;437(7063):1299-320. doi: 10.1038/nature04226.
8
Brain-derived neurotrophic factor (Val66Met) genetic polymorphism is associated with substance abuse in males.脑源性神经营养因子(Val66Met)基因多态性与男性药物滥用有关。
Brain Res Mol Brain Res. 2005 Oct 31;140(1-2):86-90. doi: 10.1016/j.molbrainres.2005.07.008. Epub 2005 Aug 18.
9
Positive association of AKT1 haplotype to Japanese methamphetamine use disorder.AKT1单倍型与日本甲基苯丙胺使用障碍的正相关关系。
Int J Neuropsychopharmacol. 2006 Feb;9(1):77-81. doi: 10.1017/S1461145705005481. Epub 2005 Jun 28.
10
A functional glutathione S-transferase P1 gene polymorphism is associated with methamphetamine-induced psychosis in Japanese population.一种功能性谷胱甘肽S-转移酶P1基因多态性与日本人群中甲基苯丙胺所致精神病相关。
Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):5-9. doi: 10.1002/ajmg.b.30164.

甲基苯丙胺依赖假定基因变异关联中种族差异的初步证据。

Preliminary evidence of ethnic divergence in associations of putative genetic variants for methamphetamine dependence.

作者信息

Bousman Chad A, Glatt Stephen J, Cherner Mariana, Atkinson J Hampton, Grant Igor, Tsuang Ming T, Everall Ian P

机构信息

Department of Psychiatry, University of California San Diego, La Jolla, CA 92103, USA.

出版信息

Psychiatry Res. 2010 Jul 30;178(2):295-8. doi: 10.1016/j.psychres.2009.07.019. Epub 2010 May 15.

DOI:10.1016/j.psychres.2009.07.019
PMID:20478633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2902702/
Abstract

Research into the biological processes that increase susceptibility to methamphetamine dependence has been conducted primarily in Asian populations. Using a case-control design this study's purpose was to explore, among a population of methamphetamine-dependent Caucasians, six putative single nucleotide polymorphisms previously found to be associated with methamphetamine dependence in Asian populations. A total of 193 non-psychotic males (117 methamphetamine-dependent and 76 controls) were genotyped for variants located in six genes (AKT1, ARRB2, BDNF, COMT, GSTP1, OPRM1). Genotypic and allelic frequencies, odds ratios, and 95% confidence intervals were calculated. None of the putative gene associations was significantly replicated in our sample of Caucasian men. Effect size comparisons suggest a trend toward allelic divergence for arrestin beta 2 (ARRB2) and glutathione S-transferase P1 (GSTP1) and allelic convergence for brain-derived neurotrophic factor (BDNF). Results provide preliminary support for further exploration and validation of candidate single nucleotide polymorphisms (SNPs) for methamphetamine (METH) dependence reported among Asian populations across other ethnic/ancestral groups.

摘要

关于增加甲基苯丙胺成瘾易感性的生物学过程的研究主要在亚洲人群中进行。本研究采用病例对照设计,目的是在甲基苯丙胺成瘾的高加索人群中,探究先前在亚洲人群中发现的六种假定的单核苷酸多态性,这些多态性与甲基苯丙胺成瘾有关。对总共193名非精神病男性(117名甲基苯丙胺成瘾者和76名对照者)进行基因分型,检测位于六个基因(AKT1、ARRB2、BDNF、COMT、GSTP1、OPRM1)中的变体。计算了基因型和等位基因频率、比值比以及95%置信区间。在我们的高加索男性样本中,没有一个假定的基因关联得到显著重复。效应大小比较表明,β-arrestin 2(ARRB2)和谷胱甘肽S-转移酶P1(GSTP1)存在等位基因差异趋势,而脑源性神经营养因子(BDNF)存在等位基因趋同趋势。研究结果为进一步探索和验证亚洲人群中报道的甲基苯丙胺(METH)成瘾候选单核苷酸多态性(SNP)在其他种族/祖先群体中的情况提供了初步支持。