SGLT2 inhibitors for the prevention of kidney failure in patients with type 2 diabetes: a systematic review and meta-analysis

Autor: David M. Charytan, Severine Bompoint, Adeera Levin, Clare Arnott, Bruce Neal, Laurent Billot, Kenneth W. Mahaffey, David C. Wheeler, Brendon L. Neuen, Vlado Perkovic, Meg Jardine, Hiddo J.L. Heerspink, Tamara Young
Rok vydání: 2019
Předmět:
medicine.medical_specialty
NEPHROPATHY
Endocrinology
Diabetes and Metabolism

medicine.medical_treatment
Renal function
PROGRESSION
030209 endocrinology & metabolism
Type 2 diabetes
DISEASE
1117 Public Health and Health Services
MECHANISMS
Nephropathy
Endocrinology & Metabolism
MELLITUS
03 medical and health sciences
0302 clinical medicine
Endocrinology
Internal medicine
Internal Medicine
medicine
Humans
Diabetic Nephropathies
030212 general & internal medicine
Sodium-Glucose Transporter 2 Inhibitors
Dialysis
Randomized Controlled Trials as Topic
RISK
OUTCOMES
Science & Technology
business.industry
EMPAGLIFLOZIN
GLOMERULAR HYPERFILTRATION
Acute kidney injury
1103 Clinical Sciences
medicine.disease
Transplantation
CONVERTING ENZYME-INHIBITORS
1101 Medical Biochemistry and Metabolomics
Albuminuria
Kidney Failure
Chronic

medicine.symptom
business
Life Sciences & Biomedicine
Kidney disease
Zdroj: The Lancet Diabetes & Endocrinology. 7:845-854
ISSN: 2213-8587
DOI: 10.1016/s2213-8587(19)30256-6
Popis: Background The effects of sodium-glucose co-transporter-2 (SGLT2) inhibitors on kidney failure, particularly the need for dialysis or transplantation or death due to kidney disease, is uncertain. Additionally, previous studies have been underpowered to robustly assess heterogeneity of effects on kidney outcomes by different levels of estimated glomerular filtration rate (eGFR) and albuminuria. We aimed to do a systematic review and meta-analysis to assess the effects of SGLT2 inhibitors on major kidney outcomes in patients with type 2 diabetes and to determine the consistency of effect size across trials and different levels of eGFR and albuminuria. Methods We did a systematic review and meta-analysis of randomised, controlled, cardiovascular or kidney outcome trials of SGLT2 inhibitors that reported effects on major kidney outcomes in people with type 2 diabetes. We searched MEDLINE and Embase from database inception to June 14, 2019, to identify eligible trials. The primary outcome was a composite of dialysis, transplantation, or death due to kidney disease. We used random-effects models to obtain summary relative risks (RRs) with 95% CIs and random-effects meta-regression to explore effect modification by subgroups of baseline eGFR, albuminuria, and use of renin–angiotensin system (RAS) blockade. This review is registered with PROSPERO (CRD42019131774). Findings From 2085 records identified, four studies met our inclusion criteria, assessing three SGLT2 inhibitors: empagliflozin (EMPA-REG OUTCOME), canagliflozin (CANVAS Program and CREDENCE), and dapagliflozin (DECLARE–TIMI 58). From a total of 38 723 participants, 252 required dialysis or transplantation or died of kidney disease, 335 developed end-stage kidney disease, and 943 had acute kidney injury. SGLT2 inhibitors substantially reduced the risk of dialysis, transplantation, or death due to kidney disease (RR 0·67, 95% CI 0·52–0·86, p=0·0019), an effect consistent across studies (I2=0%, pheterogeneity=0·53). SGLT2 inhibitors also reduced end-stage kidney disease (0·65, 0·53–0·81, p
Databáze: OpenAIRE