TY - JOUR
T1 - Irritability and its clinical utility in major depressive disorder
T2 - Prediction of individual-level acute-phase outcomes using early changes in irritability and depression severity
AU - Jha, Manish K.
AU - Minhajuddin, Abu
AU - South, Charles
AU - Rush, A. John
AU - Trivedi, Madhukar H.
N1 - Funding Information:
Presented in part as an abstract at the 2018 World Congress of the In-ternationalCollegeofNeuropsychopharmacology,Vienna,June19,2018. Supported by NIMH grant N01 MH-90003 to the University of Texas Southwestern Medical Center at Dallas (principal investigators, Drs. Rush and Trivedi) and in part by the Center for Depression Research and Clinical Care (principal investigator, Dr. Trivedi) and the Hersh Foundation. Forest Pharmaceuticals, GlaxoSmithKline, Organon, and Wyeth Pharmaceuticals provided medications for the Combining Medications to Enhance Depression Outcomes trial at no cost. The authors thank the clinical staff at each clinical site for their assistance, all of the study participants, and Eric Nestler, M.D., Ph.D., and Carol A. Tamminga, M.D., for administrative support.
Funding Information:
with Janssen Asia Pacific and Oxford University Press; and he has received grant support from the Agency for Healthcare Research and Quality, the Cancer Prevention and Research Institute of Texas, Johnson & Johnson, NIDA, the National Institute of Diabetes and Digestive and Kidney Diseases, the National Center for Advancing Translational Sciences, NIMH, and the Patient-Centered Outcomes Research Institute. The other authors report no financial relationships with commercial interests.
Funding Information:
Dr. Jha has received contract research funding from Acadia Pharmaceutical and Janssen Research and Development. Dr. Rush has received consulting fees from Akili, Brain Resource, Compass, Curbstone Consultant LLC, Eli Lilly, Emmes Corp, LivaNova, MindLinc, Sunovion, Takeda USA, and Taj Medical; he has received speaking fees from LivaNova and SingHealth; he receives royalties from Guilford Press and the University of Texas Southwestern Medical Center, Dallas; and he is co-inventor on two patents (number 7,795,033: Methods to Predict the Outcome of Treatment with Antidepressant Medication; number 7,906,283: Methods to Identify Patients at Risk of Developing Adverse Events During Treatment with Antidepressant Medication). Dr. Trivedi has served as a consultant for or on the advisory board of Alkeremes, Akili Interactive, Allergan Pharmaceuticals, Acadia Pharmaceuticals, Avanir Pharmaceuticals, Brintellix Global, Bristol-Myers Squibb, Caudex, Cerecor, Forest Pharmaceuticals, Global Medical Education, Health Research Associates, Insys, Johnson & Johnson Pharmaceutical Research and Development, Lilly Research Laboratories, Lundbeck Research USA, Medscape, Merck, Mitsubishi Pharma, MSI Methylation Sciences, Navitor, One Carbon Therapeutics, Otsuka America Pharmaceutical, Pamlab, Pfizer, and Takeda Global Research; he has received royalties from Janssen Research and Development and has author agreements
Publisher Copyright:
© 2019 American Psychiatric Association. All rights reserved.
PY - 2019/5
Y1 - 2019/5
N2 - Objective: The authors evaluated improvement in irritability with antidepressant treatment and its prognostic utility in treatment-seeking adult outpatients with major depressive disorder. Methods: Mixed-model analyses were used to assess changes in irritability (as measured with the five-item irritability domain of the Concise Associated Symptom Tracking [CAST-IRR] scale) from baseline to week 4 after controlling for depression severity (as measured with the 16-item Quick Inventory of Depressive Symptomatology–Clinician Rated [QIDS-C]) in the Combining Medications to Enhance Depression Outcomes (CO-MED) trial (N=664). An interactive calculator for remission (QIDS-C score #5) and no meaningful benefit (,30% reduction in QIDS-C score from baseline) at week 8 was developed with logistic regression analyses in the CO-MED trial using participants with complete data (N=431) and independently replicated in the Suicide Assessment and Methodology Study (SAMS) (N=163). Results: In the CO-MED trial, irritability was significantly reduced (effect size=1.06) from baseline to week 4, and this reduction remained significant after adjusting for QIDS-C change (adjusted effect size=0.36). A one-standard-deviation greater reduction in CAST-IRR score from baseline to week 4 predicted a 1.73 times higher likelihood of remission and a 0.72 times lower likelihood of no meaningful benefit at week 8, independent of baseline QIDS-C and CAST-IRR scores and reduction in QIDS-C score from baseline to week 4. The model estimates for remission (area under the curve [AUC]= 0.79) and no meaningful benefit (AUC=0.76) in the CO-MED trial were used to predict remission (AUC=0.80) and no meaningful benefit (AUC=0.84) in SAMS and to develop an interactive calculator. Conclusions: Irritability is an important symptom domain of major depressive disorder that is not fully reflected in depressive symptom severity measures. Early reductions in irritability, when combined with changes in depressive symptom severity, provide a robust estimate of likelihood of remission or no meaningful benefit in outpatients with major depression.
AB - Objective: The authors evaluated improvement in irritability with antidepressant treatment and its prognostic utility in treatment-seeking adult outpatients with major depressive disorder. Methods: Mixed-model analyses were used to assess changes in irritability (as measured with the five-item irritability domain of the Concise Associated Symptom Tracking [CAST-IRR] scale) from baseline to week 4 after controlling for depression severity (as measured with the 16-item Quick Inventory of Depressive Symptomatology–Clinician Rated [QIDS-C]) in the Combining Medications to Enhance Depression Outcomes (CO-MED) trial (N=664). An interactive calculator for remission (QIDS-C score #5) and no meaningful benefit (,30% reduction in QIDS-C score from baseline) at week 8 was developed with logistic regression analyses in the CO-MED trial using participants with complete data (N=431) and independently replicated in the Suicide Assessment and Methodology Study (SAMS) (N=163). Results: In the CO-MED trial, irritability was significantly reduced (effect size=1.06) from baseline to week 4, and this reduction remained significant after adjusting for QIDS-C change (adjusted effect size=0.36). A one-standard-deviation greater reduction in CAST-IRR score from baseline to week 4 predicted a 1.73 times higher likelihood of remission and a 0.72 times lower likelihood of no meaningful benefit at week 8, independent of baseline QIDS-C and CAST-IRR scores and reduction in QIDS-C score from baseline to week 4. The model estimates for remission (area under the curve [AUC]= 0.79) and no meaningful benefit (AUC=0.76) in the CO-MED trial were used to predict remission (AUC=0.80) and no meaningful benefit (AUC=0.84) in SAMS and to develop an interactive calculator. Conclusions: Irritability is an important symptom domain of major depressive disorder that is not fully reflected in depressive symptom severity measures. Early reductions in irritability, when combined with changes in depressive symptom severity, provide a robust estimate of likelihood of remission or no meaningful benefit in outpatients with major depression.
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U2 - 10.1176/appi.ajp.2018.18030355
DO - 10.1176/appi.ajp.2018.18030355
M3 - Article
C2 - 30922100
AN - SCOPUS:85065508544
SN - 0002-953X
VL - 176
SP - 358
EP - 366
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 5
ER -