Title of article :
Sodium-glucose co-transporter 2 inhibitors (SGLT2i); as a preventive factor of kidney failure in patients with type 2 diabetes; a meta-analysis of randomized controlled trials
Author/Authors :
Jahangiri, Dorsa Department of Internal Medicine - Isfahan University of Medical Sciences, Isfahan, Iran , Narayan Padhi, Udit Department of Zoology - Guru Ghasidas Vishwavidyalaya, Bilaspur, India , Kumar Verma, Henu Department of Immunopathology - Institute of lungs Biology and Disease - Comprehensive Pneumology Center, Helmholtz Zentrum, Neuherberg, Munich, Germany , Valizadeh, Rohollah Department of Epidemiology - School of Public Health - Iran University of Medical Sciences, Tehran, Iran , Nasri, Hamid Department of Internal Medicine - Isfahan University of Medical Sciences, Isfahan, Iran
Abstract :
Introduction: Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are a new class of anti-
diabetic drugs. SGLT2 inhibitors lower blood glucose levels by decreasing glucose reabsorption
in the proximal renal tubule, resulting in increased urinary glucose and sodium excretion.
Objective: This study was conducted to investigate the effects of SGLT2i on individual renal
outcomes in diabetic patients.
Methods: This study was a systematic review and meta-analysis of clinical trials. A
comprehensive search of Cochrane Central Register of Controlled Trials was conducted in the
Cochrane Library and PubMed, to identify relevant articles focusing on SGLT2i and chronic
kidney disease (CKD) in diabetic patients. The most recent article search was conducted on
July 12, 2021.
Results: Seven randomized controlled trials (RCTs) were included in the meta-analysis.
Two trials were comparing dapagliflozin, two comparing empagliflozin, one comparing
ertugliflozin, one comparing canagliflozin, and one comparing sotagliflozin. Composite
renal outcome and acute kidney injury (AKI) was found in seven and four studies, respectively.
Data on end-stage kidney disease (ESKD) and albuminuria or initiation of renal replacement
therapy were reported in the two studies. The pooled risk ratio (RR) 95% confidence interval
(CI) for the composite renal outcome was 0.54 (0.50–0.59), with 92 % heterogeneity. The
pooled RR for AKI was 0.77 (0.66–0.89), with no heterogeneity. A significant lower incidence
of albuminuria (RR: 0.69; 95% CI: 0.59–0.81), initiation of renal replacement therapy (RR:
0.71; 95% CI: 0.58–0.87), was observed following the use of SGLT2 inhibitors.
Conclusion: Our findings confirm that the SGLT2 inhibitors can reduce the risk of
albuminuria, AKI and renal replacement therapy in ESKD patients with T2D (type 2 diabetes).
These meta-analyses provide substantial evidence supporting the beneficial effect of SGLT2
inhibitors on reducing CKD events in individuals with T2D.
Keywords :
Sodium-glucose transporter 2 inhibitors , Chronic kidney disease , Type 2 diabetes mellitus , Acute kidney injury , Meta-analysis
Journal title :
Journal of Renal Injury Prevention