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血清素转运体和受体基因的多态性:物质滥用易感性

Polymorphisms of the serotonin transporter and receptor genes: susceptibility to substance abuse.

作者信息

Herman Aryeh I, Balogh Kornelia N

机构信息

Department of Psychiatry, VA Connecticut Healthcare/Yale University School of Medicine, West Haven, CT, USA.

出版信息

Subst Abuse Rehabil. 2012 Jun;3(1):49-57. doi: 10.2147/SAR.S25864.

Abstract

Serotonin (5-hydroxytryptamine [5-HT]) is an important neurotransmitter implicated in regulating substance-use disorder (SUD) acquisition, maintenance, and recovery. During the past several years, an abundance of research has begun discovering and describing specific 5-HT genetic polymorphisms associated with SUDs. Genetic variations in the 5-HT system, such as SLC6A4, HTR1B, HTR2A, HTR2C, HTR3 (HTR3A, HTR3B, HTR3C, HTR3D, and HTR3E), likely play a role contributing to SUD patient heterogeneity. The 5-HT transporter-linked polymorphic region S allele, located in SLC6A4, has now been modestly associated with alcohol dependence in two large meta-analyses. Additional 5-HT genes may also play a role but have not been extensively investigated. A limited number of SUD treatment studies have included 5-HT gene variation as moderating treatment outcomes, but the results have been equivocal. Future research on 5-HT addiction genetics should adopt whole-genome sequencing technology, utilize large study samples, and collect data from multiple ethnic groups. Together, these methods will build on the work already conducted with the aim of utilizing 5-HT genetics in SUD treatment settings.

摘要

血清素(5-羟色胺[5-HT])是一种重要的神经递质,与物质使用障碍(SUD)的获得、维持和康复调节有关。在过去几年中,大量研究已开始发现并描述与SUD相关的特定5-HT基因多态性。5-HT系统中的基因变异,如SLC6A4、HTR1B、HTR2A、HTR2C、HTR3(HTR3A、HTR3B、HTR3C、HTR3D和HTR3E),可能在导致SUD患者异质性方面发挥作用。位于SLC6A4中的5-HT转运体相关多态性区域S等位基因,现已在两项大型荟萃分析中与酒精依赖存在适度关联。其他5-HT基因可能也起作用,但尚未得到广泛研究。少数SUD治疗研究将5-HT基因变异作为调节治疗结果的因素,但结果并不明确。未来关于5-HT成瘾遗传学的研究应采用全基因组测序技术,利用大型研究样本,并从多个种族群体收集数据。总之,这些方法将在已开展的工作基础上,致力于在SUD治疗环境中利用5-HT遗传学。

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