Effectiveness of pharmacogenomic tests including CYP2D6 and CYP2C19 genomic variants for guiding the treatment of depressive disorders: Systematic review and meta-analysis of randomised controlled trials

Neurosci Biobehav Rev. 2023 Jan:144:104965. doi: 10.1016/j.neubiorev.2022.104965. Epub 2022 Dec 1.

Abstract

Major depressive disorders are prevalent conditions with limited treatment response and remission. Pharmacogenomics tests including CYP2D6 and CYP2C19 genomic variants provide the most reliable actionable approach to guide choice and dosing of antidepressants in major depression to improve outcomes. We carried out a meta-analysis and meta-regression analyses of randomised controlled trials evaluating pharmacogenomic tests with CYP2D6 and CYP2C19 polymorphisms in major depression. A systematic review was conducted according to PRISMA and Cochrane guidelines to search several electronic databases. Logarithmically transformed odds ratios (OR) and confidence intervals (CI) for improvement, response and remission were calculated. A random-effects meta-analysis and meta-regression analyses were subsequently carried out. Twelve randomised controlled trials were included. Pharmacogenomic tests in the treatment of depression were more effective than treatment as usual for improvement (OR:1.63, CI: 1.19-2.24), response (OR: 1.46; CI: 1.16-1.85) and remission (OR: 1.85; CI: 1.23-2.76) with no evidence of publication bias. Remission was less favourable in recent studies. The results are promising but cautious use of pharmacogenomics in major depression is advisable. PROSPERO registration ID: CRD42021261143.

Keywords: CYP2C19; CYP2D6; CYP450; Depressive disorders; Major depression; Mood disorders; Pharmacogenetics; Pharmacogenomics.

Publication types

  • Meta-Analysis
  • Systematic Review
  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytochrome P-450 CYP2C19 / genetics
  • Cytochrome P-450 CYP2D6 / genetics
  • Depressive Disorder, Major* / drug therapy
  • Depressive Disorder, Major* / genetics
  • Genomics
  • Humans
  • Pharmacogenetics
  • Randomized Controlled Trials as Topic

Substances

  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 CYP2C19
  • CYP2C19 protein, human