Can sodium-glucose co-transporter-2 (SGLT-2) inhibitor reduce the risk of adverse complications due to COVID-19? - Targeting hyperinflammation

被引:19
作者
Alshnbari, Afnan [1 ]
Idris, Iskandar [1 ,2 ,3 ]
机构
[1] Univ Nottingham, Royal Derby Hosp Ctr, Uttoxeter Rd, Derby DE22 3DT, England
[2] Univ Nottingham, NIHR, MRC Versus Arthrit Ctr Musculoskeletal Ageing Re, Nottingham BRC, Nottingham, England
[3] Univ Hosp Derby & Burton NHS Fdn Trust, Dept Endocrinol & Diabet, Derby, England
关键词
Sodium glucose co-transporter 2; inflammation; COVID; coronavirus; cardiovascular disease; CORONAVIRUS DISEASE 2019; CLINICAL CHARACTERISTICS; CYTOKINE STORM; HOSPITALIZED-PATIENTS; EMPAGLIFLOZIN; INFLAMMATION; DAPAGLIFLOZIN; HYPERGLYCEMIA; TYPE-1; CANAGLIFLOZIN;
D O I
10.1080/03007995.2022.2027141
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sodium-glucose co-transporter-2 (SGLT-2) inhibitors are antidiabetic drugs with numerous pleiotropic and positive clinical effects, particularly regarding a reno-cardiovascular protective effect. More recent studies, including from our laboratory, have highlighted some novel anti-inflammatory activity of SGLT-2 inhibitors. This may confer a theoretical advantage in mitigating excessive cytokine production and inflammatory response associated with serious COVID-19 infection. Specifically, earlier research has demonstrated that SGLT-2 inhibitors are associated with a notable decrease in inflammatory indicators, for example, C-reactive protein, ferritin, and interleukin-6. Furthermore, SGLT-2 inhibitors exhibit a favourable impact on the vascular endothelium function; this could pertinence the prophylaxis of the thrombotic issues that arise in SARS-CoV-2. This review provides an overview of the COVID-19 indirect immune response mechanisms impacting the cardiovascular system and the possible effect of SGLT-2 inhibitors on the management of COVID-19.
引用
收藏
页码:357 / 364
页数:8
相关论文
共 64 条
[1]   Association of Cardiovascular Disease With Coronavirus Disease 2019 (COVID-19) Severity: A Meta-Analysis [J].
Aggarwal, Gaurav ;
Cheruiyot, Isaac ;
Aggarwal, Saurabh ;
Wong, Johnny ;
Lippi, Giuseppe ;
Lavie, Carl J. ;
Henry, Brandon M. ;
Sanchis-Gomar, Fabian .
CURRENT PROBLEMS IN CARDIOLOGY, 2020, 45 (08)
[2]  
Alshnbari, 2019, SGLT 2 INHIBITORS IN
[3]  
Alshnbari RK., 2021, DIABETIC MED, P80
[4]   Diuretic Effects of Sodium Glucose Cotransporter 2 Inhibitors and Their Influence on the Renin-Angiotensin System [J].
Ansary, Tuba M. ;
Nakano, Daisuke ;
Nishiyama, Akira .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (03)
[5]   Associations of type 1 and type 2 diabetes with COVID-19-related mortality in England: a whole-population study [J].
Barron, Emma ;
Bakhai, Chirag ;
Kar, Partha ;
Weaver, Andy ;
Bradley, Dominique ;
Ismail, Hassan ;
Knighton, Peter ;
Holman, Naomi ;
Khunti, Kamlesh ;
Sattar, Naveed ;
Wareham, Nicholas J. ;
Young, Bob ;
Valabhji, Jonathan .
LANCET DIABETES & ENDOCRINOLOGY, 2020, 8 (10) :813-822
[6]   Issues of Cardiovascular Risk Management in People With Diabetes in the COVID-19 Era [J].
Ceriello, Antonio ;
Standl, Eberhard ;
Catrinoiu, Doina ;
Itzhak, Baruch ;
Lalic, Nebojsa M. ;
Rahelic, Dario ;
Schnell, Oliver ;
Skrha, Jan ;
Valensi, Paul .
DIABETES CARE, 2020, 43 (07) :1427-1432
[7]   Pathogenic human coronavirus infections: causes and consequences of cytokine storm and immunopathology [J].
Channappanavar, Rudragouda ;
Perlman, Stanley .
SEMINARS IN IMMUNOPATHOLOGY, 2017, 39 (05) :529-539
[8]   Renal Hemodynamic Effect of Sodium-Glucose Cotransporter 2 Inhibition in Patients With Type 1 Diabetes Mellitus [J].
Cherney, David Z. I. ;
Perkins, Bruce A. ;
Soleymanlou, Nima ;
Maione, Maria ;
Lai, Vesta ;
Lee, Alana ;
Fagan, Nora M. ;
Woerle, Hans J. ;
Johansen, Odd Erik ;
Broedl, Uli C. ;
von Eynatten, Maximilian .
CIRCULATION, 2014, 129 (05) :587-597
[9]   Cytokine storm and sepsis disease pathogenesis [J].
Chousterman, Benjamin G. ;
Swirski, Filip K. ;
Weber, Georg F. .
SEMINARS IN IMMUNOPATHOLOGY, 2017, 39 (05) :517-528
[10]  
Conti P, 2020, J BIOL REG HOMEOS AG, V34, P327, DOI 10.23812/CONTI-E