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Abstract

Coexisting general medical illness accounts for much of the previously reported association between use of nonsteroidal anti-inflammatory drugs (NSAIDs) and nonremission of treated depression. A modest but smaller relationship for NSAIDs remained when analyses included the comorbidity of patients in a large health care system and in the STAR*D study of antidepressant effectiveness. Resistance to antidepressant treatment is related to long-term NSAID use but not to intermittent use or to use of cyclo-oxygenase-2 (COX-2) inhibitors and salicylates.

Abstract

Objective

It has been suggested that there is a mechanism by which nonsteroidal anti-inflammatory drugs (NSAIDs) may interfere with antidepressant response, and poorer outcomes among NSAID-treated patients were reported in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study. To attempt to confirm this association in an independent population-based treatment cohort and explore potential confounding variables, the authors examined use of NSAIDs and related medications among 1,528 outpatients in a New England health care system.

Method

Treatment outcomes were classified using a validated machine learning tool applied to electronic medical records. Logistic regression was used to examine the association between medication exposure and treatment outcomes, adjusted for potential confounding variables. To further elucidate confounding and treatment specificity of the observed effects, data from the STAR*D study were reanalyzed.

Results

NSAID exposure was associated with a greater likelihood of depression classified as treatment resistant compared with depression classified as responsive to selective serotonin reuptake inhibitors (odds ratio=1.55, 95% CI=1.21–2.00). This association was apparent in the NSAIDs-only group but not in those using other agents with NSAID-like mechanisms (cyclooxygenase-2 inhibitors and salicylates). Inclusion of age, sex, ethnicity, and measures of comorbidity and health care utilization in regression models indicated confounding; association with outcome was no longer significant in fully adjusted models. Reanalysis of STAR*D results likewise identified an association in NSAIDs but not NSAID-like drugs, with more modest effects persisting after adjustment for potential confounding variables.

Conclusions

These results support an association between NSAID use and poorer antidepressant outcomes in major depressive disorder but indicate that some of the observed effect may be a result of confounding.

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Supplementary Material

Supplementary Material (1065_ds001.pdf)

Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 1065 - 1072
PubMed: 23032386

History

Received: 1 September 2011
Revision received: 12 March 2012
Accepted: 14 May 2012
Published online: 1 October 2012
Published in print: October 2012

Authors

Affiliations

Patience J. Gallagher, B.S.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Victor Castro, B.S.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Maurizio Fava, M.D.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Jeffrey B. Weilburg, M.D.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Shawn N. Murphy, M.D., Ph.D.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Vivian S. Gainer, M.S.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Susanne E. Churchill, Ph.D.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Isaac S. Kohane, M.D., Ph.D.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Dan V. Iosifescu, M.D., M.Sc.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Jordan W. Smoller, M.D., Sc.D.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.
Roy H. Perlis, M.D., M.Sc.
From the Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston; Partners Research Computing, Partners HealthCare System, Boston; Depression Clinic and Research Program, Department of Psychiatry, Massachusetts General Hospital; Department of Neurology, Massachusetts General Hospital; Information Systems, Partners HealthCare System; Department of Medicine, Brigham and Women’s Hospital, Boston; Department of Psychiatry, Mount Sinai School of Medicine, New York.

Notes

Address correspondence to Dr. Perlis ([email protected]).

Funding Information

Supported by the National Library of Medicine award U54LM008748 (to Dr. Kohane) and NIMH grant R01MH-086026 (to Dr. Perlis).

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