Literature DB >> 17884451

Peroxisome proliferator-activated receptor gamma agonist improves arterial stiffness in patients with type 2 diabetes mellitus and coronary artery disease.

Jie Yu1, Nan Jin, Guang Wang, Fuchun Zhang, Jieming Mao, Xian Wang.   

Abstract

Arterial stiffness is an independent risk factor for cardiovascular events in diabetic patients, and it can be assessed by measuring pulse wave velocity (PWV). We investigated the degree of arterial stiffness in diabetic patients with coronary artery disease (CAD) and the effect of the proliferator-activated receptor gamma (PPAR-gamma) agonist rosiglitazone on arterial stiffness in the potential mechanism of anti-arteriosclerosis in patients with type 2 diabetes mellitus and CAD. The 123 participants were divided into 3 groups: healthy controls (n = 36), diabetic patients (n = 41), and diabetic patients with CAD (n = 46). Forty-six diabetic patients with CAD were randomly divided into 2 groups: untreated diabetic patients with CAD and diabetic patients with CAD treated with 4 mg/d of rosiglitazone (n = 25) for 12 weeks. Pulse wave velocity was measured before treatment and at 12-week follow-up. Baseline PWV was significantly higher in patients with diabetes, diabetes and CAD, and diabetes and CAD with treatment as compared with the healthy control group (1,633 +/- 37.3, 1,669 +/- 53.8, 1,615 +/- 44.4, and 1,360 +/- 39.9 cm/s, respectively, P < .001). Pulse wave velocity in the rosiglitazone-treated group was significantly reduced, from 1,615 +/- 44.4 to 1,525 +/- 43.1 cm/s, after 12-week treatment, Furthermore, PWV was significantly decreased in the rosiglitazone-treated group compared with untreated group after 12 weeks (1525 +/- 43.1 and 1,670 +/- 41.3 cm/s, respectively). Pulse wave velocity in the untreated group did not differ from baseline levels after 12 weeks. In addition, plasma C-reactive protein level was decreased significantly in the rosiglitazone-treated group compared with values at baseline and for the untreated group after 12 weeks (0.73 +/- 0.09, 1.71 +/- 0.24, and 1.33 +/- 0.29 mg/L, respectively). Plasma level of monocyte chemoattractant protein 1 was decreased in the rosiglitazone group compared with the level at baseline (392 +/- 42 and 273 +/- 40 pg/mL, respectively). Moreover, the decrease in PWV was associated linearly both with improved homeostasis model assessment of insulin resistance and with decreased C-reactive protein level after PPAR-gamma agonist treatment. In conclusion, PPAR-gamma agonist rosiglitazone treatment may significantly decrease arterial stiffness in diabetic patients with CAD. Proliferator-activated receptor gamma agonists may play an important role in protecting against arteriosclerosis by normalizing the metabolic disorders and depressing chronic inflammation of the vascular system in patients with type 2 diabetes mellitus and serious vascular disease.

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Year:  2007        PMID: 17884451     DOI: 10.1016/j.metabol.2007.05.011

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


  13 in total

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2.  PPARγ activator, rosiglitazone: Is it beneficial or harmful to the cardiovascular system?

Authors:  Siripong Palee; Siriporn Chattipakorn; Arintaya Phrommintikul; Nipon Chattipakorn
Journal:  World J Cardiol       Date:  2011-05-26

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Review 4.  Therapeutic modification of arterial stiffness: An update and comprehensive review.

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6.  Effects of thiazolidinedione therapy on inflammatory markers of type 2 diabetes: a meta-analysis of randomized controlled trials.

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7.  Drug therapies and presence of coronary artery disease may affect aortic stiffness in Alzheimer's disease.

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8.  Antidiabetic rosiglitazone reduces soluble intercellular adhesion molecule-1 level in type 2 diabetic patients with coronary artery disease.

Authors:  Guang Wang; Zhe Zhang; Jie Yu; Fuchun Zhang; Liyun He; Jinru Wei; Jieming Mao; Xian Wang
Journal:  PPAR Res       Date:  2008-12-18       Impact factor: 4.964

Review 9.  Arterial stiffness and cardiovascular therapy.

Authors:  Miodrag Janić; Mojca Lunder; Mišo Sabovič
Journal:  Biomed Res Int       Date:  2014-08-07       Impact factor: 3.411

Review 10.  Breaking the mold: transcription factors in the anucleate platelet and platelet-derived microparticles.

Authors:  Katie L Lannan; Julie Sahler; Nina Kim; Sherry L Spinelli; Sanjay B Maggirwar; Olivier Garraud; Fabrice Cognasse; Neil Blumberg; Richard P Phipps
Journal:  Front Immunol       Date:  2015-02-13       Impact factor: 7.561

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