Imaging genetics: Perspectives from studies of genetically driven variation in serotonin function and corticolimbic affective processing

被引:233
作者
Hariri, Ahmad R.
Drabant, Emily M.
Weinberger, Daniel R.
机构
[1] Univ Pittsburgh, Sch Med, Western Psychiat Inst & Clin, Dev Imaging Genom Program,Dept Psychiat, Pittsburgh, PA 15213 USA
[2] NIMH, Genet Cognit & Psychosis Program, IRP, NIH,DHHS, Bethesda, MD 20892 USA
关键词
emotion; mood disorders; serotonin; amygdala; prefrontal cortex; neuroimaging; genetics;
D O I
10.1016/j.biopsych.2005.11.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Advances in molecular biology and neuroimaging have provided a unique opportunity to explore the relationships between genes, brain, and behavior. In this review, we will briefly outline the rationale for studying genetic effects on brain Junction with neuroimaging. We will then use studies of genetically driven variation in serotonin transporter function on corticolimbic structure and function to highlight the effectiveness of this strategy to delineate biological pathways and mechanisms by which individual differences in brain function emerge and potentially bias behavior and risk for psychiatric illness. In a series of studies, a relatively frequent regulatory variant of the human serotonin transporter gene (5-HTTLPR) has been demonstrated to bias the reactivity of the amygdala to salient environmental cues. Moreover, the 5-HTTLPR affects the development of a broader corticolimbic circuit and alters the Junctional integration of emotional information between the amygdala and, medial prefrontal cortex. In turn, corticolimbic circuit reflect a predictive,function Predicts individual differences in an experimental index of temperamental anxiety and, thus, might re biological marker of increased risk for mood disorders associated with the 5-HTTLPR.
引用
收藏
页码:888 / 897
页数:10
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