Abstract | AIMS: METHODS AND RESULTS: The study sample comprised 339 non-diabetic obese patients (body mass index > or = 30.0 kg/m2) aged 42-74. Patients received either bezafibrate retard 400 mg (178 patients) or placebo (161 patients) once daily. Development of new diabetes was recorded in 98 patients: in 56 (37.0%) from the placebo group vs. 42 (27.1%) from the bezafibrate group, (P log-rank=0.01). The median time (interquartile range) until onset of new diabetes was significantly delayed in patients on bezafibrate when compared with those on placebo: 4.0 (2.1-5.0) vs. 2.0 (0.5-3.5) years, P=0.002. Multivariable analysis identified bezafibrate treatment as an independent predictor of reduced risk of new diabetes with hazard ratio (HR) 0.59 [95% confidence interval (CI) 0.39-0.91]. Other significant variables associated with future overt type 2 diabetes in obese patients were triglycerides (50 mg/dL increment) with HR 1.15 (95% CI 1.02-1.28) and fasting glucose (10 mg/dL increment) with HR 2.27 (95% CI 1.83-2.81). CONCLUSION:
Bezafibrate, when compared with placebo, reduced the incidence and delayed the onset of type 2 diabetes in obese patients over a long-term follow-up period.
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Authors | Alexander Tenenbaum, Michael Motro, Enrique Z Fisman, Yehuda Adler, Joseph Shemesh, David Tanne, Jonathan Leor, Valentina Boyko, Ehud Schwammenthal, Solomon Behar |
Journal | European heart journal
(Eur Heart J)
Vol. 26
Issue 19
Pg. 2032-8
(Oct 2005)
ISSN: 0195-668X [Print] England |
PMID | 15872029
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial)
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Chemical References |
- Blood Glucose
- Hypolipidemic Agents
- Lipids
- Bezafibrate
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Topics |
- Adult
- Aged
- Bezafibrate
(therapeutic use)
- Blood Glucose
(metabolism)
- Body Mass Index
- Diabetes Mellitus, Type 2
(complications, metabolism, prevention & control)
- Female
- Humans
- Hypolipidemic Agents
(therapeutic use)
- Lipids
(blood)
- Male
- Middle Aged
- Obesity
(complications, metabolism)
- Prospective Studies
- Treatment Outcome
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