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Published online May 29, 2007
Diabetes Care 30:2148-2153, 2007
DOI: 10.2337/dc07-0141
© 2007 by the American Diabetes Association
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Reviews/Commentaries/ADA Statements
Meta-Analysis

Thiazolidinediones and Heart Failure

A teleo-analysis

Sonal Singh, MD1, Yoon K. Loke, MBBS, MD2 and Curt D. Furberg, MD, PHD3

1 Section of General Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina
2 School of Medicine, Health Policy and Practice, University of East Anglia, Norwich, U.K.
3 Division of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina

Address correspondence and reprint requests to Sonal Singh, Section of General Internal Medicine, Wake Forest University School of Medicine, 1 Medical Center Blvd., Winston-Salem, NC 27157. E-mail: sosingh{at}wfubmc.edu

ABSTRACT

OBJECTIVE—Thiazolidinediones (TZDs) are known to increase the risk of heart failure in patients with type 2 diabetes. We aimed to evaluate the magnitude of the risk of heart failure with TZDs and classify this adverse effect under the novel dose-time-susceptibility system.

RESEARCH DESIGN AND METHODS—Evidence from randomized trials, controlled observational studies, anecdotal case reports, case series, and spontaneous reports in the Canadian Drug Reaction Monitoring Program (CADRMP) was analyzed in a teleo-analysis.

RESULTS—A random-effects meta-analysis of three randomized controlled trials showed an odds ratio (OR) of 2.1 (95% CI 1.08–4.08; P = 0.03) for the risk of heart failure in patients randomized to TZDs compared with placebo. Four observational studies revealed an OR of 1.55 (1.33–1.80; P < 0.00001) for heart failure with TZDs. A dose-time-susceptibility analysis of 28 published reports and 214 spontaneous reports from the CADRMP database showed that heart failure was more likely to occur after several months (with median treatment duration of 24 weeks after initiation of therapy). Heart failure equally occurred at high and low doses. The adverse reaction was not limited to the elderly, with 42 of 162 (26%) of the reported cases occurring in patients aged <60 years.

CONCLUSIONS—Our teleo-analysis confirms the increased magnitude of the risk of heart failure with TZDs. We estimate the number needed to harm with TZDs to be ~50 over 2.2 years. Existing guidelines and package inserts may have to be revised to incorporate these risk characteristics of TZDs.

Abbreviations: CADRMP, Canadian Drug Reaction Monitoring Program • NYHA, New York Heart Association • RCT, randomized controlled trial • TZD, thiazolidinedione


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