Citation

Little K, Olsson CA, Youssef GJ, Whittle S, Simmons JG, Yücel M, Sheeber LB, Foley DL, Allen NB. J. Abnorm. Psychol. 2015; 124(4): 834-849.

Affiliation

Melbourne School of Psychological Sciences, Orygen Youth Health Research Centre, Centre for Youth Mental Health, University of Melbourne.

Copyright

(Copyright © 2015, American Psychological Association)

DOI

10.1037/abn0000101

PMID

26595471

Abstract

A single imaging gene-environment (IGxE) framework that is able to simultaneously model genetic, neurobiological, and environmental influences on psychopathology outcomes is needed to improve understanding of how complex interrelationships between allelic variation, differences in neuroanatomy or neuroactivity, and environmental experience affect risk for psychiatric disorder. In a longitudinal study of adolescent development we demonstrate the utility of such an IGxE framework by testing whether variation in parental behavior at age 12 altered the strength of an imaging genetics pathway, involving an indirect association between allelic variation in the serotonin transporter gene to variation in hippocampal volume and consequent onset of major depressive disorder by age 18.

RESULTS were consistent with the presence of an indirect effect of the serotonin transporter S-allele on depression onset via smaller left and right hippocampal volumes that was significant only in family environments involving either higher levels of parental aggression or lower levels of positive parenting. The previously reported finding of S-allele carriers' increased risk of depression in adverse environments may, therefore, be partly because of the effects of these environments on a neurobiological pathway from the serotonin transporter gene to depression onset that proceeds through variation in hippocampal volume. (PsycINFO Database Record

Language: en