This web page was created programmatically, to learn the article in its authentic location you possibly can go to the hyperlink bellow:
https://journals.viamedica.pl/acta_angiologica/article/view/106536
and if you wish to take away this text from our web site please contact us
Advancements in translational analysis and an more and more refined understanding of the pathophysiological mechanisms underlying vascular and metabolic illnesses have contributed to the emergence of novel therapeutic methods in sufferers with peripheral artery illness (PAD). Among these, rising consideration has been directed in the direction of the usage of glucagon-like peptide-1 receptor agonists (GLP-1 RAs), and to a lesser extent glucagon-like peptide-2 (GLP-2), as adjuncts to traditional remedy. Beyond their glucose-lowering properties, these brokers exhibit cardioprotective, cytoprotective, vasoprotective and anti inflammatory results, together with useful modulation of microcirculation and train tolerance. This narrative evaluate goals to synthesise scientific, obser-vational and experimental knowledge concerning the impression of GLP-1 and GLP-2 receptor agonists on cardiovascular danger and practical parameters in sufferers with T2DM and PAD. The evaluation integrates the 2024 European Society of Cardiology (ESC) tips for PAD administration, which emphasise the “four pillars” of therapy and introduces the idea of GLP-1 RAs as a possible “fifth pillar” in an built-in therapeutic strategy. Particular consideration is dedicated to mechanisms of motion, results on intermittent claudication signs, and the potential to enhance high quality of life in a inhabitants characterised by excessive vascular danger.
Keywords:
GLP-1 receptor agonistsperipheral artery illnessmicrocirculation
This web page was created programmatically, to learn the article in its authentic location you possibly can go to the hyperlink bellow:
https://journals.viamedica.pl/acta_angiologica/article/view/106536
and if you wish to take away this text from our web site please contact us
This web page was created programmatically, to learn the article in its authentic location you…
This web page was created programmatically, to learn the article in its unique location you…
This web page was created programmatically, to learn the article in its unique location you…
This web page was created programmatically, to learn the article in its authentic location you…
This web page was created programmatically, to learn the article in its unique location you…
This web page was created programmatically, to learn the article in its authentic location you'll…