4.7 Article

Genetic testing for CYP2D6 and CYP2C19 suggests improved outcome for antidepressant and antipsychotic medication

Journal

PSYCHIATRY RESEARCH
Volume 279, Issue -, Pages 111-115

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.psychres.2018.02.055

Keywords

Pharmacogenetics; Psychiatric medication; Personalized medicine; Clinical; Genetics

Categories

Funding

  1. Canadian Institutes of Health Research (CIHR) [MOP 142192]
  2. National Institutes of Health [R01MH085801]
  3. Centre for Addiction and Mental Health Foundation (Joanne Murphy Professorship)
  4. Brain & Behaviour Research (NARSAD) Independent Investigator Award
  5. Michael Smith New Investigator Salary Prize for Research in Schizophrenia (CIHR)
  6. Ministry of Research and Innovation of Ontario
  7. University of Toronto, Ontario
  8. NARSAD 2010 Young Investigator Award
  9. Charite Universitatsmedizin Berlin
  10. Berlin Institute of Health

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Individuals carrying genetic variants that result in non-extensive CYP2D6 and CYP2C19 enzyme activity seem to be more prone to non-response and side-effects of psychotropic medications. Therefore, tailoring prescriptions using genetic information may improve patient outcomes. This study examined treatment outcome in psychiatric care after CYP2D6 and CYP2C19 genetic information was provided to patients and physicians. CYP2D6 and CYP2C19 genotyping, assessment of side effects and medical histories were obtained from 80 subjects who were prescribed either antidepressant or antipsychotic medications. Our measure of outcome was mainly physicians' opinions however UKU side effects scores were also used. For CYP2D6, we calculated an activity score based on genotype and psychiatric medications. Correlation analysis was performed for CYP2D6 activity scores and UKU scores. Overall, we received supportive responses from physicians who enrolled patients in our study. Notably, while almost every fourth physician reported improvement in patient outcome, not a single physician indicated that their patient's symptoms worsened after they had used a pharmacogenetic report to guide treatment. We did not observe statistically significant differences in side effects. Overall, our results suggest improved patient outcome following pharmacogenetic testing; nonetheless, more research is required to assess the exact benefit of pharmacogenetics in clinical practice.

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