Epistatic interactions of AKT1 on human medial temporal lobe biology and pharmacogenetic implications

H. Y. Tan, A. G. Chen, Q. Chen, L. B. Browne, B. Verchinski, B. Kolachana, F. Zhang, J. Apud, J. H. Callicott, V. S. Mattay, D. R. Weinberger

Research output: Contribution to journalArticlepeer-review

31 Scopus citations


AKT1 controls important processes in medial temporal lobe (MTL) development and plasticity, but the impact of human genetic variation in AKT1 on these processes is not known in healthy or disease states. Here, we report that an AKT1 variant (rs1130233) previously associated with AKT1 protein expression, prefrontal function and schizophrenia, affects human MTL structure and memory function. Further, supporting AKT1's role in transducing hippocampal neuroplasticity and dopaminergic processes, we found epistasis with functional polymorphisms in BDNF and COMTgenes also implicated in MTL biology related to AKT1. Consistent with prior predictions that these biologic processes relate to schizophrenia, we found epistasis between the same AKT1, BDNF and COMT functional variants on schizophrenia risk, and pharmacogenetic interactions of AKT1 with the effects on cognition and brain volume measures by AKT1 activators in common clinical uselithium and sodium valproate. Our findings suggest that AKT1 affects risk for schizophrenia and accompanying cognitive deficits, at least in part through specific genetic interactions related to brain neuroplasticity and development, and that these AKT1 effects may be pharmacologically modulated in patients.

Original languageEnglish (US)
Pages (from-to)1007-1016
Number of pages10
JournalMolecular psychiatry
Issue number10
StatePublished - Oct 2012
Externally publishedYes


  • BDNF
  • COMT
  • hippocampus
  • lithium
  • schizophrenia
  • valproate

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience
  • Molecular Biology


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