Literature DB >> 14760320

High fasting glucose levels as a predictor of worse clinical outcome in patients with coronary artery disease: results from the Bezafibrate Infarction Prevention (BIP) study.

Lidia Arcavi1, Solomon Behar, Avraham Caspi, Naama Reshef, Valentina Boyko, Hilla Knobler.   

Abstract

BACKGROUND: A high fasting glucose level may be a marker not only for microvascular complications, but also for macrovascular complications. We evaluated the clinical significance of a high fasting glucose level (> or =110 mg/dL), detected either at baseline or during follow-up, in the Bezafibrate Infarction Prevention (BIP) study.
METHODS: The BIP study was a secondary prevention prospective double-blind study comparing bezafibrate to placebo. A total of 3122 patients with documented coronary artery heart disease who were aged 45 to 74 years and had a total cholesterol level between 180 and 250 mg/dL, low-density lipoprotein cholesterol level < or =180 mg/dL, a high-density lipoprotein cholesterol level < or =45 mg/dL, a triglyceride level < or =300 mg/dL, and a fasting glucose < or =160 mg/dL were randomized to receive 400 mg of bezafibrate daily or placebo.
RESULTS: The primary end point of the BIP study was fatal myocardial infarction, non-fatal myocardial infarction, or sudden death. Secondary end points included hospitalization for unstable angina, percutaneous transluminal coronary angioplasty, and coronary artery bypass grafting. At baseline, 330 patients (11%) had diabetes mellitus, and 293 patients (9%) had an impaired fasting blood glucose level (IFG). During 6.2 years of follow-up, diabetes mellitus developed in 186 patients (6%), IFG developed in 366 patients (12%), and 62% of patients remained with normal fasting glucose levels (NFG). Patients with diabetes mellitus and IFG both at baseline or developing during follow-up had a significantly higher rate of secondary end points than paients with NFG (P <.0001). Bezafibrate treatment reduced secondary end points only in patients with NFG (P =.04).
CONCLUSION: Diabetes mellitus and IFG were common in the BIP study and were predictive of a worse clinical outcome that was not attenuated with bezafibrate treatment.

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Year:  2004        PMID: 14760320     DOI: 10.1016/j.ahj.2003.09.013

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  6 in total

1.  Impaired fasting glucose and the risk of incident diabetes mellitus and cardiovascular events in an adult population: MESA (Multi-Ethnic Study of Atherosclerosis).

Authors:  Joseph Yeboah; Alain G Bertoni; David M Herrington; Wendy S Post; Gregory L Burke
Journal:  J Am Coll Cardiol       Date:  2011-07-05       Impact factor: 24.094

Review 2.  Fibrate therapy in patients with metabolic syndrome and diabetes mellitus.

Authors:  Thomas Dayspring; Gregory Pokrywka
Journal:  Curr Atheroscler Rep       Date:  2006-09       Impact factor: 5.113

3.  Oral glucose tolerance test is needed for appropriate classification of glucose regulation in patients with coronary artery disease: a report from the Euro Heart Survey on Diabetes and the Heart.

Authors:  M Bartnik; L Rydén; K Malmberg; J Ohrvik; K Pyörälä; E Standl; R Ferrari; M Simoons; J Soler-Soler
Journal:  Heart       Date:  2006-08-11       Impact factor: 5.994

4.  Fasting but not postprandial (postmeal) glycemia predicts the risk of death in subjects with coronary artery disease.

Authors:  Anil Nigam; Martial G Bourassa; Annik Fortier; Marie-Claude Guertin; Jean-Claude Tardif
Journal:  Can J Cardiol       Date:  2007-09       Impact factor: 5.223

Review 5.  The Microvascular and Macrovascular Benefits of Fibrates in Diabetes and the Metabolic Syndrome: A review.

Authors:  Pavan Malur; Arthur Menezes; James J DiNicolantonio; James H O'Keefe; Carl J Lavie
Journal:  Mo Med       Date:  2017 Nov-Dec

6.  PPAR Agonists and Cardiovascular Disease in Diabetes.

Authors:  Anna C Calkin; Merlin C Thomas
Journal:  PPAR Res       Date:  2008       Impact factor: 4.964

  6 in total

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