Effectiveness of pharmacogenomic tests including CYP2D6 and CYP2C19 genomic variants for guiding the treatment of depressive disorders: Systematic review and meta-analysis of randomized controlled trialsShow others and affiliations
2023 (English)In: Neuroscience and Biobehavioral Reviews, ISSN 0149-7634, E-ISSN 1873-7528, Vol. 144, article id 104965Article, review/survey (Refereed) Published
Abstract [en]
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 outcome. 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.
Place, publisher, year, edition, pages
Pergamon Press, 2023. Vol. 144, article id 104965
Keywords [en]
CYP2C19, CYP2D6, CYP450, Pharmacogenomics, depressive disorders, major depression, mood disorders, pharmacogenetics
National Category
Psychiatry
Identifiers
URN: urn:nbn:se:oru:diva-102525DOI: 10.1016/j.neubiorev.2022.104965ISI: 000900837400001PubMedID: 36463971Scopus ID: 2-s2.0-85144318147OAI: oai:DiVA.org:oru-102525DiVA, id: diva2:1716186
Note
Funding agencies:
National Institute for Health's College London
United Arab Emirates University 31M449
2022-12-052022-12-052024-03-27Bibliographically approved