β-Blockers and Depression: The More the Murkier?

Author:

Ried L Douglas1,McFarland Bentson H2,Johnson Richard E3,Brody Kathleen K4

Affiliation:

1. L Douglas Ried PhD, Associate Professor, Department of Pharmacy Health Care Administration, College of Pharmacy, University of Florida, Gainesville, FL; and Adjunct Investigator, Center for Health Research, Kaiser Permanente Northwest Region, Portland, OR

2. Bentson H McFarland MD PhD, Adjunct Investigator, Center for Health Research, Kaiser Permanente Northwest Region; and Associate Professor of Psychiatry, Public Health and Preventive Medicine, Oregon Health Sciences University, Portland, OR

3. Richard E Johnson PhD, Senior Investigator, Center for Health Research, Kaiser Permanente Northwest Region

4. Kathleen K Brody BSN PHN, Social Health Maintenance Organization Project Administrator, Center for Health Research, Kaiser Permanente Northwest Region

Abstract

OBJECTIVE: To review the literature regarding the purported association between oral ingestion of β-blocker drugs and depressed mood. DATA SOURCE: MEDLINE was searched for published articles using the key words propranolol, atenolol, metoprolol, nadolol, timolol, β-blocker, β-adrenergic antagonist, or β-adrenergic blocker in combination with the key words depression, depressive symptomatology, major depressive disorder, or depressed mood from January 1966 through December 1996. DATA SYNTHESIS: Findings regarding the association are equivocal. Plausible explanations include study design, case definition, and confounding disease states. Most of the evidence supporting an association has used case series and case reports. Findings from cross-sectional observational studies and case–control studies are equivocal. Case definition and measurement instruments may partially explain these inconsistencies. Studies using a diagnosis of depression generally do not support the relationship. Trials using depressive symptoms are about evenly split, but they have generally enrolled a small number of patients and have questionable statistical power. Studies defining antidepressant prescriptions dispensed as a marker for depression generally support the association. Evidence exists both for and against the hypothesis that lipophilic β-blockers cause more depression than do hydrophilic β-blockers. CONCLUSIONS: β-Blockers may have been unjustly associated with depression and their use avoided for that reason. Future studies into the association between depression and β-blocker use should evaluate whether the association is affected by case definition and study design characteristics, including disease, dose–response, bias, measurement error, or ability to precisely measure the length of the exposure.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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