Department of Neurology, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Alcohol Clin Exp Res. 2010 Dec;34(12):2169-78. doi: 10.1111/j.1530-0277.2010.01293.x.
Significant evidence has accumulated to suggest an association between single-nucleotide polymorphisms (SNPs) in the GABRA2 gene and alcoholism. However, research has yet to show an association between these polymorphisms and the human brain's reward system function. In this study, we stratified subjects who had participated in an fMRI study of alcohol cue responses according to their genotype at a SNP in GABRA2 (rs279871) shown to be associated with alcohol dependence (Edenberg et al., 2004).
Genotyping showed 13 subjects to be homozygous for the high-risk allele (AA), and 23 subjects to be heterozygous (AG). In fMRI, subjects were exposed to the aromas of their preferred alcoholic drink odors (AO), as well as to appetitive control odors (ApCO) under both alcohol intoxication and placebo control conditions.
Homozygous AA subjects had a larger [AO > ApCO] response than did AG subjects in medial frontal cortical areas thought to code reward value. However, AG subjects had a larger [AO > ApCO] effect in the ventral tegmental area. Alcohol intoxication did not alter these group differences.
These are the first data to suggest that GABRA2 genotype could affect the brain's responses to cues associated with alcohol.
大量证据表明,GABRA2 基因中的单核苷酸多态性(SNPs)与酗酒之间存在关联。然而,研究尚未表明这些多态性与人类大脑的奖励系统功能之间存在关联。在这项研究中,我们根据 GABRA2 基因中与酒精依赖相关的 SNP(rs279871)的基因型对参加酒精线索反应 fMRI 研究的受试者进行分层(Edenberg 等人,2004)。
基因分型显示 13 名受试者为高风险等位基因(AA)纯合子,23 名受试者为杂合子(AG)。在 fMRI 中,受试者暴露于他们喜欢的酒精饮料气味(AO)以及在酒精中毒和安慰剂对照条件下的开胃控制气味(ApCO)。
在被认为编码奖励价值的额内侧皮质区域中,AA 纯合子受试者的[A0 > ApCO]反应大于 AG 受试者。然而,AG 受试者在腹侧被盖区的[A0 > ApCO]效应更大。酒精中毒并未改变这些组间差异。
这些是第一个表明 GABRA2 基因型可能影响与酒精相关线索的大脑反应的研究数据。