Pharmacogenomic Clinical Support Tools for the Treatment of Depression
This article has been corrected.
VIEW CORRECTIONPublication: American Journal of Psychiatry
Abstract
Objective:
In this review, the authors update the 2018 report of the American Psychiatric Association Council of Research Workgroup on Biomarkers and Novel Treatments on pharmacogenomic (PGx) tools for treatment selection in depression.
Methods:
The literature was reviewed for new clinical trials and meta-analyses, published from 2017 to 2022, of studies using PGx tools for treatment selection in depression. The blinding and control conditions, as well as primary and secondary outcomes and post hoc analyses, were summarized.
Results:
Eleven new clinical trials and five meta-analyses were identified; all studies had primary outcome measures related to speed or efficacy of treatment response. Three trials (27%) demonstrated efficacy on the primary outcome measure with statistical significance; the three studies used different PGx tools; one study was open-label and the other two were small single-blind trials. Five trials (45%) did not detect efficacy with statistical significance on either primary or secondary outcome measures. Only one trial (9%) used adverse events as a primary outcome measure. All studies had significant limitations; for example, none adopted a fully blinded study design, only two studies attempted to blind the treating clinician, and none incorporated measures to estimate the effectiveness of the blinds or the influence of lack of blinding on the study results.
Conclusions:
The addition of these new data do not alter the recommendations of the 2018 report, or the advice of the U.S. Food and Drug Administration, that the evidence does not support the use of currently available combinatorial PGx tools for treatment selection in major depressive disorder. Priority efforts for future studies and the development and testing of effective tools include fully blinded study designs, inclusion of promising genetic variants not currently included in any commercially available tests, and investigation of other uses of pharmacogenomics, such as estimating the likelihood of rare adverse drug effects, rather than increasing the speed or magnitude of drug response.
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History
Received: 21 August 2023
Revision received: 30 October 2023
Revision received: 5 December 2023
Revision received: 4 January 2024
Accepted: 17 January 2024
Published online: 30 April 2024
Published in print: July 01, 2024
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Competing Interests
Dr. Baum receives royalties from Oxford University Press. Dr. Widge has received donations of deep brain stimulation devices from Medtronic and consulting fees from Abbott, and he holds multiple granted and pending patents related to deep brain stimulation. Dr. Carpenter has received research support from Affect Neuro, Janssen Pharmaceuticals, Neuronetics, Neurolief, Nexstim, and SynapseBio, and she has served as a scientific adviser or consultant for Affect Neuro, Janssen Pharmaceuticals, Neuronetics, Neurolief, Nexstim, Otsuka, Sage Therapeutics, and Sunovion. Dr. McDonald is a Deputy Editor of the American Journal of Psychiatry; disclosures of Editors’ financial relationships appear in the April 2024 issue of the Journal. Dr. Nemeroff has served as a consultant for AbbVie, ANeuroTech, Autobahn Therapeutics, BioXcel Therapeutics, Clexio, EMA Wellness, EmbarkNeuro, Engrail Therapeutics, GoodCap Pharmaceuticals, Guidepoint, Intra-Cellular Therapies, Magstim, Ninnion Therapeutics, Pasithea Therapeutics Corp., Relmada Therapeutics, Sage, Senseye, Signant Health, Silo Pharma, and SynapseBio; he is a stockholder in Antares, Corcept Therapeutics, EMA Wellness, Naki Health, PreciseMent Health, Relmada Therapeutics, and Seattle Genetics; he has served on scientific advisory boards for ANeuroTech, the Anxiety and Depression Association of America (ADAA), the Brain and Behavior Research Foundation, Galen Health, Heading Health, the Laureate Institute for Brain Research, Pasithea Therapeutics Corp., Sage, Signant Health, and Skyland Trail and on the boards of directors for ADAA, Gratitude America, and Lucy Scientific Discovery; and he is named on patents on a method and devices for transdermal delivery of lithium and a method of assessing antidepressant drug therapy via transport inhibition of monoamine neurotransmitters by ex vivo assay. Dr. Cohen reports no financial relationships with commercial interests.
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