Targeting Diabetic Atherosclerosis: The Role of GLP-1 Receptor Agonists, SGLT2 Inhibitors, and Nonsteroidal Mineralocorticoid Receptor Antagonists in Vascular Protection and Disease Modulation

被引:0
|
作者
Rroji, Merita [1 ,2 ]
Spahia, Nereida [2 ]
Figurek, Andreja [3 ]
Spasovski, Goce [4 ]
机构
[1] Univ Med Tirana, Dept Nephrol, Tirana 1001, Albania
[2] Univ Hosp Ctr Mother Tereza, Dept Nephrol, Tirana 1001, Albania
[3] Univ Zurich, Inst Anat, CH-8057 Zurich, Switzerland
[4] Univ Sts Cyril & Methodius, Dept Nephrol, Skopje 1000, North Macedonia
关键词
diabetic kidney disease; atherosclerosis; endothelial dysfunction; oxidative stress; inflammation; GLUCAGON-LIKE PEPTIDE-1; CHRONIC KIDNEY-DISEASE; FOAM CELL-FORMATION; STAGE RENAL-DISEASE; INSULIN-RESISTANCE; OXIDATIVE STRESS; CARDIOVASCULAR RISK; DOUBLE-BLIND; ENDOTHELIAL DYSFUNCTION; ADIPOSE-TISSUE;
D O I
10.3390/biomedicines13030728
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atherosclerosis is a closely related complication of diabetes mellitus (DM), driven by endothelial dysfunction, inflammation, and oxidative stress. The progression of atherosclerosis is accelerated by hyperglycemia, insulin resistance, and hyperlipidemia. Novel antidiabetic agents, SGLT2 inhibitors, and GLP-1 agonists improve glycemic control and offer cardiovascular protection, reducing the risk of major adverse cardiovascular events (MACEs) and heart failure hospitalization. These agents, along with nonsteroidal mineralocorticoid receptor antagonists (nsMRAs), promise to mitigate metabolic disorders and their impact on endothelial function, oxidative stress, and inflammation. This review explores the potential molecular mechanisms through which these drugs may prevent the development of atherosclerosis and cardiovascular disease (CVD), supported by a summary of preclinical and clinical evidence.
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页数:42
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