4.7 Review

Neuregulin-1 and schizophrenia in the genome-wide association study era

Journal

NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
Volume 68, Issue -, Pages 387-409

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neubiorev.2016.06.001

Keywords

Neuregulin 1; Schizophrenia; Psychosis; Excitatory neurotransmission; Inhibitory neurotransmission; Neuroimaging; Genotype; Transcript

Funding

  1. Cooperative Research Centre for Mental Health Top-up Scholarship
  2. One-in-Five Association Incorporated
  3. NHMRC [628386]
  4. Brain and Behavior Research Foundation (NARSAD) Distinguished Investigator Award
  5. National Health and Medical Research Council (NHMRC) [1045643, 1102012]
  6. Rebecca L. Cooper Medical Research Foundation Ltd.
  7. Schizophrenia Research Institute (from the NSW Ministry of Health)
  8. Schizophrenia Research Institute (from the Macquarie Group Foundation)
  9. University of New South Wales
  10. Neuroscience Research Australia
  11. National Health and Medical Research Council (Australia) [1021970]
  12. University of Melbourne Ronald Phillip Griffith Fellowship
  13. Brain and Behavior Research Foundation (NARSAD) Young Investigator Award [20526]

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Clinical and pre-clinical evidence has implicated neuregulin 1 (NRG1) as a critical component in the pathophysiology of schizophrenia. However, the arrival of the genome-wide association study (GWAS) era has yielded results that challenge the relevance of NRG1 in schizophrenia due to the absence of a genome-wide significant NRG1 variant associated with schizophrenia. To assess NRG1's relevance to schizophrenia in the GWAS era, we provide a targeted review of recent preclinical evidence on NRG1's role in regulating several aspects of excitatory/inhibitory neurotransmission and in turn schizophrenia risk. We also present a systematic review of the last decade of clinical research examining NRG1 in the context of schizophrenia. We include concise summaries of genotypic variation, gene-expression, protein expression, structural and functional neuroimaging as well as cognitive studies conducted during this time period. We conclude with recommendations for future clinical and preclinical work that we hope will help prioritize a strategy forward to further advance our understanding of the relationship between NRG1 and schizophrenia. (C) 2016 Elsevier Ltd. All rights reserved.

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