Sodium-glucose co-transporter-2 inhibitors for the prevention of cardiorenal outcomes in type 2 diabetes: An updated meta-analysis.
Dario GiuglianoMiriam LongoPaola CarusoMaria Ida MaiorinoGiuseppe BellastellaKatherine EspositoPublished in: Diabetes, obesity & metabolism (2021)
A meta-analysis of cardiorenal outcomes of sodium-glucose co-transporter-2 inhibitors (SGLT-2is) available in Europe or the United States in patients with type 2 diabetes (T2D) is presented. An electronic search up to 6 January 2021 was conducted to determine eligible trials. A total of eight cardiorenal outcomes trials of SGLT-2is (empagliflozin, canagliflozin, dapagliflozin, ertugliflozin and sotagliflozin) were identified, with 65,587 patients. Data were analysed using a random effects model. Overall, SGLT-2is were associated with a 12% reduced risk of major adverse cardiovascular events (MACE; HR = 0.88; 95% CI, 0.83-0.93; Q statistic, p = .19), with no significant heterogeneity (p for interaction = .465) between subgroups of patients with or without cardiovascular disease (CVD). The risk of the composite renal outcome was significantly reduced by treatment with SGLT-2is (HR = 0.61, 95% CI, 0.54-0.70), with no significant heterogeneity of associations with outcome (I2 = 37%, p = .11), and no difference in the risk between patients with or without CVD (p for interaction = .665). SGLT-2is have moderate benefits on MACE and major benefits on the progression of diabetic kidney disease.
Keyphrases
- cardiovascular events
- cardiovascular disease
- type diabetes
- systematic review
- end stage renal disease
- glycemic control
- coronary artery disease
- ejection fraction
- single cell
- newly diagnosed
- peritoneal dialysis
- emergency department
- insulin resistance
- patient reported outcomes
- deep learning
- cardiovascular risk factors
- patient reported
- drug induced