Age-related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescence

Authors

  • Jillian Lee Wiggins,

    Corresponding author
    1. Department of Psychology, University of Michigan, Ann Arbor, Michigan
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  • Jirair K. Bedoyan,

    1. Department of Pediatrics, Division of Pediatric Genetics, University of Michigan, Ann Arbor, Michigan
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  • Melisa Carrasco,

    1. Neuroscience Program, University of Michigan, Ann Arbor, Michigan
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  • Johnna R. Swartz,

    1. Department of Psychology, University of Michigan, Ann Arbor, Michigan
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  • Donna M. Martin,

    1. Department of Pediatrics, Division of Pediatric Genetics, University of Michigan, Ann Arbor, Michigan
    2. Neuroscience Program, University of Michigan, Ann Arbor, Michigan
    3. Department of Human Genetics, University of Michigan, Ann Arbor, Michigan
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  • Christopher S. Monk

    1. Department of Psychology, University of Michigan, Ann Arbor, Michigan
    2. Neuroscience Program, University of Michigan, Ann Arbor, Michigan
    3. Department of Psychiatry, University of Michigan, Ann Arbor, Michigan
    4. Center for Human Growth and Development, University of Michigan, Ann Arbor, Michigan
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Abstract

The S and LG alleles of the serotonin transporter-linked polymorphic region (5-HTTLPR) lower serotonin transporter expression. These low-expressing alleles are linked to increased risk for depression and brain activation patterns found in depression (increased amygdala activation and decreased amygdala–prefrontal cortex connectivity). Paradoxically, serotonin transporter blockade relieves depression symptoms. Rodent models suggest that decreased serotonin transporter in early life produces depression that emerges in adolescence, whereas decreased serotonin transporter that occurs later in development ameliorates depression. However, no brain imaging research has yet investigated the moderating influence of human development on the link between 5-HTTLPR and effect-related brain function. We investigated the age-related effect of 5-HTTLPR on amygdala activation and amygdala–prefrontal cortex connectivity using a well-replicated probe, an emotional face task, in children and adolescents aged 9–19 years. A significant genotype-by-age interaction predicted amygdala activation, such that the low-expressing genotype (S/S and S/LG) group showed a greater increase in amygdala activation with age compared to the higher expressing (LA/LA and S/LA) group. Additionally, compared to the higher expressing group, the low-expressing genotype group exhibited decreased connectivity between the right amygdala and ventromedial prefrontal cortex with age. Findings indicate that low-expressing genotypes may not result in the corticolimbic profile associated with depression risk until later adolescence. Hum Brain Mapp 35:646–658, 2014. © 2012 Wiley-Periodicals, Inc.

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