Recommendations for selection and adaptation of rating scales for clinical studies of rapid-acting antidepressants
- PMID: 37333908
- PMCID: PMC10272853
- DOI: 10.3389/fpsyt.2023.1135828
Recommendations for selection and adaptation of rating scales for clinical studies of rapid-acting antidepressants
Abstract
The novel mechanisms of action (MOA) derived from some recently introduced molecular targets have led to regulatory approvals for rapid acting antidepressants (RAADs) that can generate responses within hours or days, rather than weeks or months. These novel targets include the N-methyl-D-glutamate receptor antagonist ketamine, along with its enantiomers and various derivatives, and the allosteric modulators of gamma-aminobutyric acid (GABA) receptors. There has also been a strong resurgence in interest in psychedelic compounds that impact a range of receptor sites including D1, 5-HT7, KOR, 5-HT5A, Sigma-1, NMDA, and BDNF. The RAADs developed from these novel targets have enabled successful treatment for difficult to treat depressed individuals and has generated a new wave of innovation in research and treatment. Despite the advances in the neurobiology and clinical treatment of mood disorders, we are still using rating instruments that were created decades ago for drugs from a different era (e.g., The Hamilton and Montgomery-Åsberg depression rating scales, HDRS, and MADRS) continue to be used. These rating instruments were designed to assess mood symptoms over a 7-day time frame. Consequently, the use of these rating instruments often requires modifications to address items that cannot be assessed in short time frames, such as the sleep and appetite items. This review describes the adaptative approaches that have been made with the existing scales to meet this need and examines additional domains such as daily activities, side effects, suicidal ideation and behavior, and role functioning. Recommendations for future studies are described, including the challenges related to implementation of these adapted measures and approaches to mitigation.
Keywords: ISCTM working group; ketamine; measurement of rapid response to anti-depressant treatment; novel anti-depressants; psychedelics; psychometrics; rapid acting anti-depressants.
Copyright © 2023 Yavorsky, Ballard, Opler, Sedway, Targum and Lenderking.
Conflict of interest statement
CY is the Chief Scientific Officer at Valis Biosciences, Inc. EB is the Director of Psychology and Behavior Research and the Director of Predoctoral Training at the Experimental Therapeutics and Pathophysiology Branch in the National Institute of Mental Health. MO is Chief Research Officer at WCG Clinical Endpoint Solutions. JS is Vice President of Clinical Science at WCG Clinical Endpoint Solutions. ST is Scientific director at Signant Health, Chief Medical Officer at Functional Neuromodulation LLC., and has had consulting relationships with Actinogen Medical Ltd., AZ Therapies, BioXcel Therapeutics, EMA Wellness, Denovo BioPharma, Frequency Therapeutics, Karuna Therapeutics Inc., Merck Pharmaceuticals, Navitor Pharmaceuticals, Neurocrine Bioscience, and Relmada Therapeutics within the past 3 years. WL is the Vice President and Executive Director of Patient Centered Research at Evidera, a PPD company.
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