Arias Albert, Feinn Richard, Kranzler Henry R
Alcohol Research Center, Department of Psychiatry, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030-2103, USA.
Drug Alcohol Depend. 2006 Jul 27;83(3):262-8. doi: 10.1016/j.drugalcdep.2005.11.024. Epub 2006 Jan 4.
The mu-opioid receptor has been implicated in the pathogenesis of dependence on opioids, alcohol, nicotine, and cocaine. Studies examining the association of the mu-opioid receptor gene (genetic locus OPRM1) with substance dependence (SD) have focused on the Asn40Asp (A118G) single nucleotide polymorphism (SNP).
We used meta-analysis to examine the literature on the association of Asn40Asp with SD. Twenty-two articles describing 28 distinct samples and over 8000 subjects were included. A variety of factors (i.e., ethnicity, type of SD, rigor with which controls were screened, severity of SD among cases) were examined as potential moderators of the association.
Four studies showed a significantly higher frequency of the Asp40 allele among SD cases, while three studies showed a significantly higher frequency of the Asp40 allele among controls. There was no significant association between Asn40Asp and SD (OR=1.01, 95%CI=0.86-1.19), nor was there substantial evidence of a moderator effect.
The Asn40Asp SNP in OPRM1 does not appear to affect risk for SD. Additional research is needed to determine whether these findings reflect no role for OPRM1 in determining risk for SD or whether another polymorphism in the gene influences receptor function and risk for SD.
μ-阿片受体与阿片类药物、酒精、尼古丁和可卡因依赖的发病机制有关。研究μ-阿片受体基因(基因座OPRM1)与物质依赖(SD)之间关联的研究主要集中在Asn40Asp(A118G)单核苷酸多态性(SNP)上。
我们采用荟萃分析来研究Asn40Asp与SD之间关联的文献。纳入了22篇描述28个不同样本和8000多名受试者的文章。研究了各种因素(即种族、SD类型、对照筛选的严格程度、病例中SD的严重程度)作为该关联的潜在调节因素。
四项研究显示SD病例中Asp40等位基因的频率显著更高,而三项研究显示对照组中Asp40等位基因的频率显著更高。Asn40Asp与SD之间没有显著关联(OR = 1.01,95%CI = 0.86 - 1.19),也没有实质性证据表明存在调节效应。
OPRM1中的Asn40Asp SNP似乎不影响SD风险。需要进一步研究以确定这些发现是反映OPRM1在确定SD风险中不起作用,还是该基因中的另一种多态性影响受体功能和SD风险。