Pioglitazone and Heart Failure: Results From a Controlled Study in Patients With Type 2 Diabetes Mellitus and Systolic Dysfunction
Abstract
Background
Thiazolidinediones are associated with fluid retention, often interpreted as worsening cardiac function, limiting their use in patients with heart failure (HF). We compared the effects of pioglitazone and glyburide on cardiac function in patients with type 2 diabetes, systolic dysfunction, and New York Heart Association (NYHA) functional Class II/III HF.
Methods and Results
Participants received pioglitazone or glyburide (±insulin) for 6 months in this double-blind, randomized, multicenter study. The primary end point was time to HF, a composite of cardiovascular mortality and hospitalization or emergency room (ER) visit for HF. Secondary endpoints included echocardiographic and functional classification assessments. An earlier time to onset and higher incidence of the primary endpoint was noted with pioglitazone (13%) versus glyburide (8%) (P = .024). Hospitalization or ER visit occurred in 30 pioglitazone and 15 glyburide participants, 19 and 12 of whom, respectively, continued treatment. Cardiac mortality (5 versus 6 participants, respectively) and cardiac function, as measured by change in ventricular mass index (P = .959), ejection fraction (P = .413), or fractional shortening (P = .280), were similar between treatments.
Conclusions
Pioglitazone was associated with a higher incidence of hospitalization for HF without an increase in cardiovascular mortality or worsening cardiac function (by echocardiography).
Key Words: Cardiovascular disease, thiazolidinediones, left ventricular dysfunction
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Sponsored and funded by Takeda Global Research & Development Center, Inc. Deerfield, Illinois.
Partial data from this study have been published previously as congress abstracts (American College of Cardiology Scientific Session 2007 and European Society of Cardiology Congress 2007).
Dr. Thomas Giles has received honoraria for speaking/consulting services and research grants from Takeda Pharmaceuticals; Dr. Allen Miller has received honoraria for speaking services from Takeda Pharmaceuticals and payment from GlaxoSmithKline for consulting services; Dr. Uri Elkayam has received honoraria for speaking/consulting services and research grants from Takeda Pharmaceuticals; Drs. Perez and Bhattacharyra are employees of Takeda Pharmaceuticals.
Funded by Takeda Pharmaceuticals (Takeda Global Research & Development).
PII: S1071-9164(08)00060-2
doi:10.1016/j.cardfail.2008.02.007
© 2008 Elsevier Inc. All rights reserved.
