4.7 Article

Oxytocin Receptor Genotype Modulates Ventral Striatal Activity to Social Cues and Response to Stressful Life Events

Journal

BIOLOGICAL PSYCHIATRY
Volume 76, Issue 5, Pages 367-376

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2013.07.043

Keywords

Amygdala; functional magnetic resonance imaging; genetics; oxytocin; social behavior; ventral striatum

Funding

  1. European Union-funded FP6 Integrated Project IMAGEN [LSHM-CT-2007-037286]
  2. German Ministry of Education and Research (BMBF) [01EV0711, eMED Alcoholism]
  3. FP7 project IMAGEMEND
  4. Innovative Medicine Initiative Project EU-AIMS [115300-2]
  5. Medical Research Council Programme Grant Developmental pathways into adolescent substance abuse [G93558]
  6. Swedish Research Council (FORMAS)
  7. United Kingdom National Institute for Health Research Biomedical Research Centre Mental Health
  8. German Federal Ministry of Education and Research
  9. AstraZeneca
  10. Eli Lilly
  11. Janssen-Cilag
  12. Bristol-Myers Squibb
  13. Medical Research Council [G0901858] Funding Source: researchfish
  14. MRC [G0901858] Funding Source: UKRI

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Background: Common variants in the oxytocin receptor gene (OXTR) have been shown to influence social and affective behavior and to moderate the effect of adverse experiences on risk for social-affective problems. However, the intermediate neurobiological mechanisms are not fully understood. Although human functional neuroimaging studies have reported that oxytocin effects on social behavior and emotional states are mediated by amygdala function, animal models indicate that oxytocin receptors in the ventral striatum (VS) modulate sensitivity to social reinforcers. This study aimed to comprehensively investigate OXTR-dependent brain mechanisms associated with social-affective problems. Methods: In a sample of 1445 adolescents we tested the effect of 23-tagging single nucleotide polymorphisms across the OXTR region and stressful life events (SLEs) on functional magnetic resonance imaging blood oxygen level-dependent activity in the VS and amygdala to animated angry faces. Single nucleotide polymorphisms for which gene-wide significant effects on brain function were found were then carried forward to examine associations with social-affective problems. Results: A gene-wide significant effect of rs237915 showed that adolescents with minor CC-genotype had significantly lower VS activity than CT/TT-carriers. Significant or nominally significant gene x environment effects on emotional problems (in girls) and peer problems (in boys) revealed a strong increase in clinical symptoms as a function of SLEs in CT/TT-carriers but not CC-homozygotes. However, in low-SLE environments, CC-homozygotes had more emotional problems (girls) and peer problems (boys). Moreover, among CC-homozygotes, reduced VS activity was related to more peer problems. Conclusions: These findings suggest that a common OXTR-variant affects brain responsiveness to negative social cues and that in riskcarriers reduced sensitivity is simultaneously associated with more social-affective problems in favorable environments and greater resilience against stressful experiences.

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