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- W2890783608 endingPage "38" @default.
- W2890783608 startingPage "29" @default.
- W2890783608 abstract "Atherosclerosis is a major underlying cause of ischemic heart diseases, ischemic stroke, and peripheral artery disease. Atherosclerotic plaque progression is characterized by chronic progressive inflammation of the arterial wall, endothelial cell dysfunction, and subendothelial lipoprotein retention. Incretin drugs, glucagon-like peptide-1 receptor (GLP-1R) agonists, and dipeptidyl peptidase-IV (DPP-IV) inhibitors, are promising anti-hyperglycemic agents used for the treatment of type 2 diabetes mellitus (T2DM). In addition to glucose-lowering effects, emerging data suggest that incretin drugs have anti-atherogenic effects with the potential to stabilize atherosclerotic plaques and treat arterial inflammation. Clinical and preclinical studies have reported a plethora of therapeutic benefits of incretin drugs, including modulation of inflammatory response, reduction of intima-media thickening, improvement in lipid profiles, endothelial and smooth muscle cell modulation. Despite extensive research and widespread clinical use of incretin-based therapies, the research on the incretin hormones continues to expand. This review outlines clinical studies, molecular aspects, and potential therapeutic implications of incretin drugs in attenuation of atherosclerosis." @default.
- W2890783608 created "2018-09-27" @default.
- W2890783608 creator A5010137044 @default.
- W2890783608 creator A5027384327 @default.
- W2890783608 creator A5046314302 @default.
- W2890783608 date "2018-11-01" @default.
- W2890783608 modified "2023-10-18" @default.
- W2890783608 title "Incretin drugs as modulators of atherosclerosis" @default.
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