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Author Notes:

Disclosures: pattiangelomaria@gmail.com (A.M.P.) or ferdinando.mannello@uniurb.it (F.M.)

Author contributions: Conceptualization, A.M.P., R.V.G. and F.M.; data curation, A.M.P., A.P.S. and A.A.R.; writing—original draft preparation, A.M.P., R.V.G. and D.L.; writing—review and editing, D.L., F.M. and A.M.P.; visualization and editing of figures, D.L. and R.V.G.; supervision, final revision, and editing F.M. All authors read and approved the final version of manuscript.

This review was written independently. The authors have given talks, attended conferences and participated in advisory boards and trials sponsored by various pharmaceutical companies that had no role in the design of the review; in the interpretation of data and in the writing of the manuscript, or in the decision to publish the results.

S.A.P. is currently the Vice President of the Romanian National Diabetes Committee. The authors are grateful to Rizzo Manfredi for his invaluable and outstanding scientific support.

Disclosures: The authors declare no conflict of interest.

Subjects:

Research Funding:

This research received no external funding. The authors did not receive financial or professional help with the preparation of the manuscript.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Medicine, General & Internal
  • General & Internal Medicine
  • cardiovascular risk
  • dipeptidyl peptidase-4 inhibitors
  • glucagon like peptide-1 receptor agonists
  • sodium glucose cotransporter-2 inhibitors
  • type 2 diabetes mellitus
  • Peptide-1 receptor agonist
  • Base line characteristics
  • Heart failure
  • Glycemic control
  • Itca 650
  • Outcomes
  • Pioglitazone
  • Exenatide
  • Safety
  • trial

Impact of Glucose-Lowering Medications on Cardiovascular and Metabolic Risk in Type 2 Diabetes

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Journal Title:

Journal of Clinical Medicine

Volume:

Volume 9, Number 4

Publisher:

Type of Work:

Article | Final Publisher PDF

Abstract:

Type 2 Diabetes Mellitus (T2DM) is associated with a high risk of atherosclerotic cardiovascular (CV) disease. Among the well-known pathophysiologic factors, crucial roles are played by endothelial dysfunction (caused by oxidative stress and inflammation hyperglycemia-linked), increased activity of nuclear factor kB, altered macrophage polarization, and reduced synthesis of resident endothelial progenitor cells. As consequence, a potentially rapid progression of the atherosclerotic disease with a higher propensity to unstable plaque is arguable, finally leading to significantly increased cardiovascular mortality. Main managements are focused on both prevention and early diagnosis, by targeted treatment of hyperglycemia and vascular complications. Innovative therapeutic approaches for T2DM seek to customize the antidiabetic treatment to each patient in order to optimize glucose-lowering effects, minimize hypoglycemia and adverse effects, and prevent cardiovascular events. The newer drugs (e.g., Glucagon Like Peptide-1 Receptor Agonists, GLP-1 RAs; Sodium GLucose coTransporter-2 inhibitors, SGLT2is; DiPeptidyl Peptidase-4 inhibitors, and DPP4is) impact body weight, lipid parameters, and blood pressure, as well as endothelial (dys)functions, inflammatory markers, biomarkers of both oxidative stress, and subclinical atherosclerosis. The present review summarizes the results of the main trials focused on the cardiovascular safety of these drugs from the CV standpoint.

Copyright information:

© 2020 by the authors. Licensee MDPI, Basel, Switzerland.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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