Literature DB >> 10726910

Bezafibrate reduces blood glucose in type 2 diabetes mellitus.

S Ogawa1, K Takeuchi, K Sugimura, M Fukuda, R Lee, S Ito, T Sato.   

Abstract

The clinical efficacy of bezafibrate was examined with special reference to glucose metabolism in patients with type 2 diabetes mellitus (DM2). In protocol 1, 342 patients with DM2 and hyperlipidemias were randomly divided into 2 groups, 16-week bezafibrate treatment (n = 174) and no bezafibrate treatment (n = 168). In protocol 2, 20 DM2 patients were randomly divided into 2 groups, 8-week bezafibrate treatment (n = 10) and no bezafibrate treatment (n = 10), and a meal tolerance test (MTT) was performed. In protocol 1, bezafibrate treatment significantly reduced the fasting levels of triglyceride (TG) by 50% +/- 1.6%, total cholesterol (TC) by 12% +/- 1.1%, plasma glucose (PG) from 151.3 +/- 3.5 to 128.6 +/- 3.4 mg/dL, and hemoglobin A1c (HbA1c) from 7.2% +/- 0.1% to 6.9% +/- 0.1%, and significantly increased high-density lipoprotein cholesterol (HDL-C) by 20% +/- 0.8%. In protocol 2, fasting TG, PG, and insulin levels were significantly reduced by bezafibrate treatment. Moreover, in the MTT, postprandial increments of TG were significantly blunted after bezafibrate treatment, whereas postprandial PG and insulin levels were not significantly changed. Leptin levels were significantly decreased, while tumor necrosis factor alpha (TNF-alpha) levels were not changed. In conclusion, both hyperglycemia and hyperlipidemia can be improved by bezafibrate treatment in DM2.

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Year:  2000        PMID: 10726910     DOI: 10.1016/s0026-0495(00)90176-8

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  12 in total

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Authors:  M Vázquez; N Roglans; A Cabrero; C Rodríguez; T Adzet; M Alegret; R M Sánchez; J C Laguna
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3.  Association between postprandial remnant-like particle triglyceride (RLP-TG) levels and carotid intima-media thickness (IMT) in Japanese patients with type 2 diabetes: assessment by meal tolerance tests (MTT).

Authors:  Yutaka Mori; Yohta Itoh; Hideaki Komiya; Naoko Tajima
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4.  Ragaglitazar: a novel PPAR alpha PPAR gamma agonist with potent lipid-lowering and insulin-sensitizing efficacy in animal models.

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Journal:  Br J Pharmacol       Date:  2003-09-01       Impact factor: 8.739

5.  Effects of nateglinide on the elevation of postprandial remnant-like particle triglyceride levels in Japanese patients with type 2 diabetes assessment by meal tolerance test.

Authors:  Yutaka Mori; Genshin Kuriyama; Naoko Tajima
Journal:  Endocrine       Date:  2004-12       Impact factor: 3.633

Review 6.  Peroxisome Proliferator-Activated Receptors and Their Agonists in Nonalcoholic Fatty Liver Disease.

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Review 7.  Fibrates are an essential part of modern anti-dyslipidemic arsenal: spotlight on atherogenic dyslipidemia and residual risk reduction.

Authors:  Alexander Tenenbaum; Enrique Z Fisman
Journal:  Cardiovasc Diabetol       Date:  2012-10-11       Impact factor: 9.951

8.  Effects of bezafibrate on lipid and glucose metabolism in dyslipidemic patients with diabetes: the J-BENEFIT study.

Authors:  Tamio Teramoto; Kohji Shirai; Hiroyuki Daida; Nobuhiro Yamada
Journal:  Cardiovasc Diabetol       Date:  2012-03-23       Impact factor: 9.951

9.  Saroglitazar, a novel PPARα/γ agonist with predominant PPARα activity, shows lipid-lowering and insulin-sensitizing effects in preclinical models.

Authors:  Mukul R Jain; Suresh R Giri; Chitrang Trivedi; Bibhuti Bhoi; Akshyaya Rath; Geeta Vanage; Purvi Vyas; Ramchandra Ranvir; Pankaj R Patel
Journal:  Pharmacol Res Perspect       Date:  2015-05-04

Review 10.  Balanced pan-PPAR activator bezafibrate in combination with statin: comprehensive lipids control and diabetes prevention?

Authors:  Alexander Tenenbaum; Enrique Z Fisman
Journal:  Cardiovasc Diabetol       Date:  2012-11-14       Impact factor: 9.951

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