Considerations for optimal use of postmortem human brains for molecular psychiatry: lessons from schizophrenia

Handb Clin Neurol. 2018:150:221-235. doi: 10.1016/B978-0-444-63639-3.00016-5.

Abstract

Schizophrenia is a disabling disease impacting millions of people around the world, for which there is no known cure. Current antipsychotic treatments for schizophrenia mainly target psychotic symptoms, do little to ameliorate social or cognitive deficits, have side-effects that cause weight gain, and diabetes and 30% of people do not respond. Thus, better therapeutics for schizophrenia aimed at the route biologic changes are needed and discovering the underlying neurobiology is key to this quest. Postmortem brain studies provide the most direct and detailed way to determine the pathophysiology of schizophrenia. This chapter outlines steps that can be taken to ensure the best-quality molecular data from postmortem brain tissue are obtained. In this chapter, we also discuss targeted and high-throughput methods for examining gene and protein expression and some of the strengths and limitations of each method. We briefly consider why gene and protein expression changes may not always concur within brain tissue. We conclude that postmortem brain research that investigates gene and protein expression in well-characterized and matched brain cohorts provides an important foundation to be considered when interpreting data obtained from studies of living schizophrenia patients.

Keywords: gene expression; mRNA; postmortem brain; protein expression; qRT-PCR; schizophrenia; transcriptomics.

Publication types

  • Review

MeSH terms

  • Biomedical Research / methods*
  • Brain / pathology*
  • Humans
  • Molecular Medicine*
  • Neurobiology
  • Schizophrenia / genetics*
  • Schizophrenia / pathology*