Abstract
Background: Many patients with major depressive disorder (MDD) who experience no meaningful benefit (NMB) from antidepressive treatment go undetected. However, there is a lack of consensus on the definition of NMB from antidepressants. Methods: Equipercentile linking was used to identify a threshold for percent change in 17-item Hamilton Depression Rating Scale (HDRS-17) scores that equated with a Clinical Global Impressions-Improvement (CGI-I) score of 3 (minimally improved), a proxy for NMB, after 4 and 8 weeks of citalopram or escitalopram treatment, using data from the Pharmacogenomic Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS). The NMB threshold for the HDRS-17 was validated by equating a CGI-I rating of 3 with percent change values from the clinician- and patient-rated versions of the Quick Inventory of Depressive Symptomatology (QIDS-C and QIDS-SR) using data from PGRN-AMPS and phase 1 of the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial. This study was conducted between June 2021 and September 2021. Results: In PGRN-AMPS, a 30% improvement in HDRS-17 score corresponded to a CGI-I rating of 3 at 4 and 8 weeks. The 30% improvement threshold was also observed for QIDS-C and QIDS-SR scores in both PGRN-AMPS and STAR*D. Similar results were observed for percent change in HDRS-17 and QIDS-based measures in lower- and higher-severity groups based on a median split of baseline total scores. Conclusions: Improvement in depressive severity of ≤ 30%, as assessed using the HDRS-17, QIDS-C, and QIDS-SR, may validly define NMB from antidepressants during short-term treatment.
Original language | English (US) |
---|---|
Article number | 21m14239 |
Journal | Journal of Clinical Psychiatry |
Volume | 83 |
Issue number | 4 |
DOIs | |
State | Published - 2022 |
ASJC Scopus subject areas
- Psychiatry and Mental health
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In: Journal of Clinical Psychiatry, Vol. 83, No. 4, 21m14239, 2022.
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}
TY - JOUR
T1 - Toward a Definition of “No Meaningful Benefit” From Antidepressant Treatment
T2 - An Equipercentile Analysis With Cross-Trial Validation Across Multiple Rating Scales
AU - Zhang, Carl
AU - Virani, Sanya
AU - Mayes, Taryn
AU - Carmody, Thomas
AU - Croarkin, Paul E.
AU - Weinshilboum, Richard
AU - Rush, A. John
AU - Trivedi, Madhukar
AU - Athreya, Arjun P.
AU - Bobo, William V.
N1 - Funding Information: Submitted: September 4, 2021; accepted January and Quality, National Science Foundation, Mayo depression: a randomized controlled trial with 10, 2022. Foundation for Medical Education and Research, blind raters. Am J Psychiatry. Publishedonline:June 27, 2022. and the Myocarditis Foundation, and he has 2015;172(10):1004–1013.PubMed CrossRef Authorcontributions:Drs Bobo and Athreya contributed chapters to UpToDate on the treatment Fortney JC, Unützer J, Wrenn G, et al. A tipping served as overall co-principal investigators and, of bipolar disorders. The other authors declared no point for measurement-based care. Psychiatr in this capacity, planned and oversaw the analysis competing interests for this work. Serv. 2017;68(2):179–188.PubMed CrossRef of study data. Drs Bobo and Athreya and Mr Funding/support: This study was supported, Kudlow PA, McIntyre RS, Lam RW. Early in part, by funds from the Mayo Foundation for switching strategies in antidepressant non-Zhang wrote the initial draft ofthe manuscript. Medical Education and Research, Mayo Clinic responders: current evidence and future findingsandsubsequentdraftsofthesubmittedAll authors contributed to the interpretation of Summer Undergraduate Research Fellowship, research directions. CNS Drugs. manuscript and approved the final manuscript. National Institute of General Medical Sciences 2014;28(7):601–609.PubMed CrossRef under grants GM61388 and GM28157, National Quitkin FM, McGrath PJ, Stewart JW, et al. Drs Bobo and Athreya had access to all data and Science Foundation under award 2041339, and Chronological milestones to guide drug take responsibility for the accuracy ofthe data National Institute of Mental Health under grant change: when should clinicians switch analysis and the writing ofthe manuscript. MH90003. The STAR*D trial was supported by antidepressants? Arch Gen Psychiatry. Relevantfinancialrelationships:Dr Carmody Bristol-Myers Squibb, Forest Pharmaceuticals, 1996;53(9):785–792.PubMed CrossRef has provided consulting services to Alkermes. GlaxoSmithKline, King Pharmaceuticals, Organon, Pae CU, Wang SM, Lee SY, et al. Early switch from Neuronetics, NeoSync, and Pfizer and has DrCroarkinhas received research grant support Pfizer, and Wyeth-Ayerst Laboratories, who strategy in patients with major depressive provided study medications. disorder. Expert Rev Neurother. received grant in-kind (equipment and supply 2012;12(10):1185–1188.PubMed CrossRef support for research studies) from Assurex Health, study had no role in the design of the study; in the Roleofthe sponsor:The sources of funding for this Nierenberg AA, DeCecco LM. Definitions of Neuronetics, and MagVenture and has served collection, analyses, or interpretation of data; in antidepressant treatment response, remission, as a consultant for Engrail Therapeutics, Myriad the writing of the manuscript; or in the decision to nonresponse, partial response, and other Neuroscience, Procter & Gamble, and Sunovion. publish the results. relevant outcomes: a focus on treatment-Dr Weinshilboum is a co-founder and stockholder resistant depression. J Clin Psychiatry. in OneOme, LLC, a pharmacogenomic clinical 2001;62(suppl 16):5–9.PubMed decision support company. Dr Rush has received Fava M, Davidson KG. Definition and consulting fees from Akili, Brain Resource, James SL, Abate D, Abate H; GBD 2017 Disease epidemiology of treatment-resistant Compass, Curbstone Consultant LLC, Emmes and Injury Incidence and Prevalence depression. Psychiatr Clin North Am. Corp.,Johnson&Johnson(Janssen),Liva-Nova, Collaborators. Global, regional, and national 1996;19(2):179–200.PubMed CrossRef Mind Linc, and Sunovion; speaking fees from incidence, prevalence, and years lived with Guy W. ECDEU Assessment Manual for JanssenandLiva-Nova;androyaltiesfromGuilford disability for 354 diseases and injuries for 195 Psychopharmacology. US Department of Press and the University of Texas Southwestern countries and territories, 1990–2017: a Health, Education, and Welfare, Public Health Medical Center, Dallas (for the Inventory of systematic analysis for the Global Burden of Service; 1976. Depressive Symptomatology and its derivatives). Disease Study 2017. Lancet. Busner J, Targum SD. The Clinical Global He is also named co-inventor on 2 patents: US 2018;392(10159):1789–1858.PubMed CrossRef Impressions scale: applying a research tool in Patent No. 7,795,033: Methods to Predict the Bromet E, Andrade LH, Hwang I, et al. Cross- clinical practice. Psychiatry (Edgmont). Outcome of Treatment with Antidepressant national epidemiology of DSM-IV major 2007;4(7):28–37.PubMed Medication and US Patent No. 7,906,283: Methods depressive episode. BMC Med. 2011;9(1):90.PubMed CrossRef Spielmans GI, McFall JP. A comparative meta-to Identify Patients at Risk of Developing Adverse Smith K. Mental health: a world of depression. analysis of Clinical Global Impressions change Events During Treatment with Antidepressant Nature. 2014;515(7526):180–181.PubMed CrossRef in antidepressant trials. J Nerv Ment Dis. Medication. Dr Trivedi has provided consulting Rush AJ, Trivedi MH, Wisniewski SR, et al. Acute 2006;194(11):845–852.PubMed CrossRef services to Acadia Pharmaceuticals, Alkermes, and longer-term outcomes in depressed Bobo WV, Angleró GC, Jenkins G, et al. Alto Neuroscience, Axsome Therapeutics, GH outpatients requiring one or several treatment Validation of the 17-item Hamilton Depression Research Limited, GreenLight VitalSign6, Janssen, steps: a STAR*D report. Am J Psychiatry. Rating Scale definition of response for adults Merck Sharp & Dohme, Mind Medicine (MindMed), 2006;163(11):1905–1917.PubMed CrossRef with major depressive disorder using Neurocrine Biosciences, Orexo US, Otsuka, Trivedi MH, Rush AJ, Wisniewski SR, et al; equipercentile linking to Clinical Global SAGE Therapeutics, Signant Health, and Titan STAR*D Study Team. Evaluation of outcomes Impression scale ratings: analysis of Pharmaceuticals, Inc, and he has received grant/ with citalopram for depression using Pharmacogenomic Research Network research funding from NIMH, National Institute on measurement-based care in STAR*D: Antidepressant Medication Drug Abuse, Patient-Centered Outcomes Research implications for clinical practice. Am J Pharmacogenomic Study (PGRN-AMPS) data. Institute, and Cancer Prevention Research Psychiatry.2006;163(1):28–40.PubMedCrossRef HumPsychopharmacol. 2016;31(3):185–192.PubMedCrossRef Institute of Texas. Additionally, he has received Carvalho AF, Berk M, Hyphantis TN, et al. The Leucht S, Fennema H, Engel R, et al. What does editorial compensation from Oxford University integrative management of treatment-the HAMD mean? J Affect Disord. 2013;148(2-Press. Dr Athreya receives funding support resistant depression: a comprehensive review 3):243–248.PubMed CrossRef from National Science Foundation and National and perspectives. Psychother Psychosom. Leucht S, Fennema H, Engel RR, et al. What Institutes of Health. Dr Bobo’s research has been 2014;83(2):70–88.PubMed CrossRef does the MADRS mean? equipercentile linking supported by the National Institute for Mental Guo T, Xiang YT, Xiao L, et al. Measurement-with the CGI using a company database of Health (NIMH), Agency for Healthcare Research based care versus standard care for major mirtazapine studies. J Affect Disord. Funding Information: This study was supported, in part, by funds from the Mayo Foundation for Medical Education and Research, Mayo Clinic Summer Undergraduate Research Fellowship, National Institute of General Medical Sciences under grants GM61388 and GM28157, National Science Foundation under award 2041339, and National Institute of Mental Health under grant MH90003. The STAR*D trial was supported by Bristol-Myers Squibb, Forest Pharmaceuticals, GlaxoSmithKline, King Pharmaceuticals, Organon, Pfizer, and Wyeth-Ayerst Laboratories, who provided study medications. Publisher Copyright: © Copyright 2022 Physicians Postgraduate Press, Inc.
PY - 2022
Y1 - 2022
N2 - Background: Many patients with major depressive disorder (MDD) who experience no meaningful benefit (NMB) from antidepressive treatment go undetected. However, there is a lack of consensus on the definition of NMB from antidepressants. Methods: Equipercentile linking was used to identify a threshold for percent change in 17-item Hamilton Depression Rating Scale (HDRS-17) scores that equated with a Clinical Global Impressions-Improvement (CGI-I) score of 3 (minimally improved), a proxy for NMB, after 4 and 8 weeks of citalopram or escitalopram treatment, using data from the Pharmacogenomic Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS). The NMB threshold for the HDRS-17 was validated by equating a CGI-I rating of 3 with percent change values from the clinician- and patient-rated versions of the Quick Inventory of Depressive Symptomatology (QIDS-C and QIDS-SR) using data from PGRN-AMPS and phase 1 of the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial. This study was conducted between June 2021 and September 2021. Results: In PGRN-AMPS, a 30% improvement in HDRS-17 score corresponded to a CGI-I rating of 3 at 4 and 8 weeks. The 30% improvement threshold was also observed for QIDS-C and QIDS-SR scores in both PGRN-AMPS and STAR*D. Similar results were observed for percent change in HDRS-17 and QIDS-based measures in lower- and higher-severity groups based on a median split of baseline total scores. Conclusions: Improvement in depressive severity of ≤ 30%, as assessed using the HDRS-17, QIDS-C, and QIDS-SR, may validly define NMB from antidepressants during short-term treatment.
AB - Background: Many patients with major depressive disorder (MDD) who experience no meaningful benefit (NMB) from antidepressive treatment go undetected. However, there is a lack of consensus on the definition of NMB from antidepressants. Methods: Equipercentile linking was used to identify a threshold for percent change in 17-item Hamilton Depression Rating Scale (HDRS-17) scores that equated with a Clinical Global Impressions-Improvement (CGI-I) score of 3 (minimally improved), a proxy for NMB, after 4 and 8 weeks of citalopram or escitalopram treatment, using data from the Pharmacogenomic Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS). The NMB threshold for the HDRS-17 was validated by equating a CGI-I rating of 3 with percent change values from the clinician- and patient-rated versions of the Quick Inventory of Depressive Symptomatology (QIDS-C and QIDS-SR) using data from PGRN-AMPS and phase 1 of the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial. This study was conducted between June 2021 and September 2021. Results: In PGRN-AMPS, a 30% improvement in HDRS-17 score corresponded to a CGI-I rating of 3 at 4 and 8 weeks. The 30% improvement threshold was also observed for QIDS-C and QIDS-SR scores in both PGRN-AMPS and STAR*D. Similar results were observed for percent change in HDRS-17 and QIDS-based measures in lower- and higher-severity groups based on a median split of baseline total scores. Conclusions: Improvement in depressive severity of ≤ 30%, as assessed using the HDRS-17, QIDS-C, and QIDS-SR, may validly define NMB from antidepressants during short-term treatment.
UR - http://www.scopus.com/inward/record.url?scp=85139762399&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85139762399&partnerID=8YFLogxK
U2 - 10.4088/JCP.21m14239
DO - 10.4088/JCP.21m14239
M3 - Article
C2 - 35771974
AN - SCOPUS:85139762399
SN - 0160-6689
VL - 83
JO - Journal of Clinical Psychiatry
JF - Journal of Clinical Psychiatry
IS - 4
M1 - 21m14239
ER -