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Summary
August 2007, Vol. 8, No. 12, Pages 1985-1998
, DOI 10.1517/14656566.8.12.1985
Pioglitazone: update on an oral antidiabetic drug with antiatherosclerotic effectsAndreas Pfützner1IKFE – Institute for Clinical Research and Development, Parcusstr. 8, D-55116 Mainz, Germany +49 6131 5763610; +49 6131 5763611; AndreasP@ikfe.de 2University Hospital, Department of Endocrinology and Metabolism, Mainz, Germany Pioglitazone, a member of the PPAR-γ agonist drug family, has been demonstrated to improve both metabolic and vascular insulin resistance when applied to patients with Type 2 diabetes mellitus. The drug is well tolerated with fluid retention and weight gain being the most frequently described side effects. The observed effects (e.g., improvements in glucose and lipid metabolism, improvements of endothelial function and microcirculation, reduction of surrogate markers of atherosclerosis and inflammation and an improvement in hypertension) have made pioglitazone one of the frequently prescribed antidiabetic drugs in the US and Europe. Several trials have shown its potency to reduce carotid intima-media thickness, and outcome studies with pioglitazone have shown its potential to delay the progression of Type 2 diabetes and atherosclerosis and even reduce cardiovascular mortality. The purpose of this review is to provide an overview about recently published clinical results with pioglitazone. They underline the value of this drug when used alone or in combination with other antidiabetic drugs for a successful management of Type 2 diabetes mellitus. Forward Links to Citing ArticlesYM He. (2008) Effects of Pollen Typhae total flavones on mRNA expressions of peroxisome proliferator-activated receptors in 3T3-L1 adipocytes. Journal of Chinese Integrative Medicine 6:9, 939-941 Online publication date: 15-Oct-2008. CrossRef Qingguang Jiang, Michael Heneka, Gary E Landreth. (2008) The Role of Peroxisome Proliferator-Activated Receptor-γ (PPARγ) in Alzheimer’s Disease. CNS Drugs 22:1, 1-14 Online publication date: 1-Feb-2008. CrossRef Users who read this article also read:
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