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Type 2 diabetes individuals are at high risk for macrovascular complications: myocardial infarction, stroke and cardiovascular mortality. Recent cardiovascular outcome trials have demonstrated that agents in two antidiabetic classes (SGLT2 inhibitors and GLP-1 receptor agonists) reduce major adverse cardiovascular events. However, there is strong evidence that an older and now generically available medication, the thiazolidinedione, pioglitazone, can retard the atherosclerotic process (PERISCOPE and Chicago) and reduce cardiovascular events in large randomized prospective cardiovascular outcome trials (IRIS and PROactive). Pioglitazone is a potent insulin sensitizer, preserves beta-cell function, causes durable reduction in HbA1c, corrects multiple components of metabolic syndrome and improves nonalcoholic fatty liver disease/nonalcoholic steatohepatitis. Adverse effects (weight gain, fluid retention, fractures) must be considered, but are diminished with lower doses and are arguably outweighed by these multiple benefits. With healthcare expenses attributable to diabetes increasing rapidly, this cost-effective drug requires reconsideration in the therapeutic armamentarium for the disease.
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Ralph A. DeFronzo
Pennington Biomedical Research Center
Silvio E. Inzucchi
University of Vermont
Muhammad Abdul-Ghani
The University of Texas Health Science Center at San Antonio
Diabetes and Vascular Disease Research
Yale University
Cleveland Clinic
The University of Texas Health Science Center at San Antonio
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DeFronzo et al. (Fri,) studied this question.
synapsesocial.com/papers/6a1c4b17b33628da419d6425 — DOI: https://doi.org/10.1177/1479164118825376