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We also provide updates on the current knowledge of pathogenesis, specificity, and treatment of the associated conditions

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Exenatide was approved by the US FDA in 2005 and by the European Medicines Agency (EMA) in 2006

Conclusion In conclusion, our study demonstrates that the use of GLP-1RAs in patients with T2D undergoing coronary stent implantation is associated with a significant reduction in major adverse cardiovascular events and coronary lesion progression

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