@article{ed1f364d5aec4e3da4155b9483f6e56c,
title = "Montgomery-{\AA}sberg Depression Rating Scale factors in treatment-resistant depression at onset of treatment: Derivation, replication, and change over time during treatment with esketamine",
abstract = "Objective: Derive and confirm factor structure of the Montgomery-{\AA}sberg Depression Rating Scale (MADRS) in patients with treatment-resistant depression (TRD) and evaluate how the factors evident at baseline change over 4 weeks of esketamine treatment. Methods: Two similarly-designed, short-term TRANSFORM trials randomized adults to esketamine or matching placebo nasal spray, each with a newly-initiated oral antidepressant, for 4 weeks (TRANSFORM-1: N = 342 patients; TRANSFORM-2: N = 223 patients). The factor structure of MADRS item scores at baseline was determined by exploratory factor analysis in TRANSFORM-2 and corroborated by confirmatory factor analysis in TRANSFORM-1. Change in MADRS factor scores from baseline (day 1) to the end of the 28-day double-blind treatment phase of TRANSFORM-2 was analyzed using a mixed-effects model for repeated measures (MMRM). Results: Three factors were identified based on analysis of MADRS items: Factor 1 labeled affective and anhedonic symptoms (apparent sadness, reported sadness, lassitude, inability to feel), Factor 2 labeled anxiety and vegetative symptoms (inner tension, reduced sleep, reduced appetite, concentration difficulties), and Factor 3 labeled hopelessness (pessimistic thoughts, suicidal thoughts). The three-factor structure observed in TRANSFORM-2 was verified in TRANSFORM-1. Treatment benefit at 24 h with esketamine versus placebo was observed on all 3 factors and continued throughout the 4-week double-blind treatment period. Conclusions: A three-factor structure for MADRS appears to generalize to TRD. All three factors improved over 4 weeks of treatment with esketamine nasal spray.",
keywords = "depression, esketamine, factor analysis, MADRS",
author = "Stephane Borentain and Jagadish Gogate and David Williamson and Thomas Carmody and Trivedi, {Madhukar H} and Carol Jamieson and Patricia Cabrera and Vanina Popova and Ewa Wajs and Allitia DiBernardo and Daly, {Ella J.}",
note = "Funding Information: Drs. Borentain, Gogate, Jamieson, Cabrera, Popova, Wajs, and DiBernardo are employees of Janssen Research & Development, LLC or Jan‐Cil Colombia, Drs. Williamson and Daly were employees of Janssen Scientific Affairs, LLC at the time this work was performed, and some authors hold company equity. Dr. Carmody has consulted for Alkermes, Inc., Dr. Trivedi has consulted for or served on the advisory board of Acadia Pharmaceuticals, Inc., Alkermes Inc., Alto Neuroscience Inc., Axsome Therapeutics, GH Research Limited, GreenLight VitalSign6 Inc., Janssen, Merck Sharp & Dohme Corp., Mind Medicine (MindMed) Inc., Neurocrine Biosciences Inc., Orexo US Inc., Otsuka, SAGE Therapeutics, Signant Health, and Titan Pharmaceuticals, Inc. Dr. Trivedi has received research support from the Cancer Prevention and Research Institute of Texas, Janssen Research & Development, LLC, National Institute of Drug Abuse, National Institute of Mental Health, and the Patient‐Centered Outcomes Research Institute; and he has received editorial compensation from Oxford University Press. Funding Information: We acknowledge Sandra Norris, PharmD, of the Norris Communications Group LLC for medical writing assistance and Ellen Baum, PhD (Janssen Global Services, LLC), for additional editorial support. This work was supported by funding from Janssen Research & Development LLC, Titusville, NJ USA. Publisher Copyright: {\textcopyright} 2022 Janssen Research & Development, LLC. International Journal of Methods in Psychiatric Research published by John Wiley & Sons Ltd.",
year = "2022",
doi = "10.1002/mpr.1927",
language = "English (US)",
journal = "International Journal of Methods in Psychiatric Research",
issn = "1049-8931",
publisher = "John Wiley and Sons Ltd",
}