Anti-inflammatory role of SGLT2 inhibitors as part of their anti-atherosclerotic activity: Data from basic science and clinical trials

被引:76
作者
Scisciola, Lucia [1 ]
Cataldo, Vittoria [1 ]
Taktaz, Fatemeh [1 ]
Fontanella, Rosaria Anna [1 ]
Pesapane, Ada [1 ]
Ghosh, Puja [1 ]
Franzese, Martina [1 ]
Puocci, Armando [1 ]
De Angelis, Antonella [2 ]
Sportiello, Liberata [2 ]
Marfella, Raffaele [1 ,3 ]
Barbieri, Michelangela [1 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Adv Med & Surg Sci, Naples, Italy
[2] Univ Campania Luigi Vanvitelli, Dept Expt Med, Sect Pharmacol L Donatelli, Naples, Italy
[3] Mediterranea Cardioctr, Naples, Italy
关键词
SGLT2 inhibitors (SGLT2i); SGLT2; atherosclerosis; atherosclerosis cardiovascular diseases; inflammation; REDUCED EJECTION FRACTION; CARDIOVASCULAR OUTCOMES; HEART-FAILURE; OXIDATIVE STRESS; VASCULAR-DISEASE; MECHANISMS; EMPAGLIFLOZIN; INFLAMMATION; SENESCENCE; ATHEROSCLEROSIS;
D O I
10.3389/fcvm.2022.1008922
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atherosclerosis is a progressive inflammatory disease leading to mortality and morbidity in the civilized world. Atherosclerosis manifests as an accumulation of plaques in the intimal layer of the arterial wall that, by its subsequent erosion or rupture, triggers cardiovascular diseases. Diabetes mellitus is a well-known risk factor for atherosclerosis. Indeed, Type 2 diabetes mellitus patients have an increased risk of atherosclerosis and its associated-cardiovascular complications than non-diabetic patients. Sodium-glucose co-transport 2 inhibitors (SGLT2i), a novel anti-diabetic drugs, have a surprising advantage in cardiovascular effects, such as reducing cardiovascular death in a patient with or without diabetes. Numerous studies have shown that atherosclerosis is due to a significant inflammatory burden and that SGLT2i may play a role in inflammation. In fact, several experiment results have demonstrated that SGLT2i, with suppression of inflammatory mechanism, slows the progression of atherosclerosis. Therefore, SGLT2i may have a double benefit in terms of glycemic control and control of the atherosclerotic process at a myocardial and vascular level. This review elaborates on the anti-inflammatory effects of sodium-glucose co-transporter 2 inhibitors on atherosclerosis.
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页数:13
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共 97 条
[1]   Dapagliflozin exerts anti-inflammatory effects via inhibition of LPS-induced TLR-4 overexpression and NF-κB activation in human endothelial cells and differentiated macrophages [J].
Abdollahi, Elaheh ;
Keyhanfar, Fariborz ;
Delbandi, Ali-Akbar ;
Falak, Reza ;
Hajimiresmaiel, Seyed Javad ;
Shafiei, Massoumeh .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2022, 918
[2]   Interleukin-6 promotes a sustained loss of endothelial barrier function via Janus kinase-mediated STAT3 phosphorylation and de novo protein synthesis [J].
Alsaffar, Hiba ;
Martino, Nina ;
Garrett, Joshua P. ;
Adam, Alejandro P. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2018, 314 (05) :C589-C602
[3]   Can sodium-glucose co-transporter-2 (SGLT-2) inhibitor reduce the risk of adverse complications due to COVID-19? - Targeting hyperinflammation [J].
Alshnbari, Afnan ;
Idris, Iskandar .
CURRENT MEDICAL RESEARCH AND OPINION, 2022, 38 (03) :357-364
[4]   SGLT2 inhibitors reduce infarct size in reperfused ischemic heart and improve cardiac function during ischemic episodes in preclinical models [J].
Andreadou, Ioanna ;
Bell, Robert M. ;
Botker, Hans Erik ;
Zuurbier, Coert J. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2020, 1866 (07)
[5]   Macrophages in Atherosclerosis Regression [J].
Barrett, Tessa J. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2020, 40 (01) :20-33
[6]  
Basatemur GL, 2019, NAT REV CARDIOL, V16, P727, DOI [10.1038/s41569-019-0227-9, 10.1161/CIRCRESAHA.115.306361]
[7]   Diabetes and vascular disease: pathophysiology, clinical consequences, and medical therapy: part II [J].
Beckman, Joshua A. ;
Paneni, Francesco ;
Cosentino, Francesco ;
Creager, Mark A. .
EUROPEAN HEART JOURNAL, 2013, 34 (31) :2444-U31
[8]   Extraglycemic Effects of SGLT2 Inhibitors: A Review of the Evidence [J].
Bonora, Benedetta Maria ;
Avogaro, Angelo ;
Fadini, Gian Paolo .
DIABETES METABOLIC SYNDROME AND OBESITY, 2020, 13 :161-174
[9]   Low-density lipoproteins cause atherosclerotic cardiovascular disease: pathophysiological, genetic, and therapeutic insights: a consensus statement from the European Atherosclerosis Society Consensus Panel [J].
Boren, Jan ;
Chapman, M. John ;
Krauss, Ronald M. ;
Packard, Chris J. ;
Bentzon, Jacob F. ;
Binder, Christoph J. ;
Daemen, Mat J. ;
Demer, Linda L. ;
Hegele, Robert A. ;
Nicholls, Stephen J. ;
Nordestgaard, Brge G. ;
Watts, Gerald F. ;
Bruckert, Eric ;
Fazio, Sergio ;
Ference, Brian A. ;
Graham, Ian ;
Horton, Jay D. ;
Landmesser, Ulf ;
Laufs, Ulrich ;
Masana, Luis ;
Pasterkamp, Gerard ;
Raal, Frederick J. ;
Ray, Kausik K. ;
Schunkert, Heribert ;
Taskinen, Marja-Riitta ;
van de Sluis, Bart ;
Wiklund, Olov ;
Tokgozoglu, Lale ;
Catapano, Alberico L. ;
Ginsberg, Henry N. .
EUROPEAN HEART JOURNAL, 2020, 41 (24) :2313-+
[10]   Cardiovascular Outcomes with Ertugliflozin in Type 2 Diabetes [J].
Cannon, Christopher P. ;
Pratley, Richard ;
Dagogo-Jack, Samuel ;
Mancuso, James ;
Huyck, Susan ;
Masiukiewicz, Urszula ;
Charbonnel, Bernard ;
Frederich, Robert ;
Gallo, Silvina ;
Cosentino, Francesco ;
Shih, Weichung J. ;
Gantz, Ira ;
Terra, Steven G. ;
Cherney, David Z. I. ;
McGuire, Darren K. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (15) :1425-1435