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Cardiovascular Outcomes of Sodium-Glucose Cotransporter-2 Inhibitors Therapy in Patients With Type 2 Diabetes Mellitus and Chronic Kidney Disease: A Systematic Review and Updated Meta-Analysis.
Felix, Nicole; Gauza, Mateus M; Teixeira, Larissa; Guisso, Maria Eduarda S; Nogueira, Alleh; Dagostin, Caroline S; Godoi, Amanda; Ribeiro, Sandro A G; Duque, Juan C; Moura-Neto, José A; Cardoso, Rhanderson.
  • Felix N; Federal University of Campina Grande, Campina Grande, PB, Brazil.
  • Gauza MM; University of the Region of Joinville, Joinville, SC, Brazil.
  • Teixeira L; Federal University of Campina Grande, Campina Grande, PB, Brazil.
  • Guisso MES; University of the Region of Joinville, Joinville, SC, Brazil.
  • Nogueira A; Bahiana School of Medicine and Public Health, Salvador, BA, Brazil.
  • Dagostin CS; University of the Extreme South of Santa Catarina, Criciúma, SC, Brazil.
  • Godoi A; Cardiff University School of Medicine, Cardiff, UK. amandacgodoi@gmail.com.
  • Ribeiro SAG; University of Brasília, Brasília, DF, Brazil.
  • Duque JC; Katz Family Division of Nephrology and Hypertension, Department of Medicine, University of Miami, Miami, FL, USA.
  • Moura-Neto JA; Bahiana School of Medicine and Public Health, Salvador, BA, Brazil.
  • Cardoso R; Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Korean Circ J ; 54(9): 549-561, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38859642
ABSTRACT
BACKGROUND AND

OBJECTIVES:

The efficacy of sodium-glucose cotransporter-2 inhibitors (SGLT2i) may depend on renal function, and this raises theoretical concern over its effects on cardiovascular outcomes in patients with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD).

METHODS:

This systematic review and updated meta-analysis of randomized controlled trials (RCTs) compared cardiovascular outcomes of patients with T2DM and CKD treated with SGLT2i to placebo. PubMed, Embase, and Cochrane were systematically searched. Prespecified subgroup analyses were performed in strata of estimated glomerular filtration rate (eGFR) of <45 mL/min/1.73 m² and 45 to 59 mL/min/1.73 m².

RESULTS:

Nine RCTs comprising 29,146 patients were selected. Average follow-up ranged from 0.75 to 4.2 years. SGLT2i were shown to reduce the risk of all-cause mortality (hazard ratio [HR], 0.88; 95% confidence interval [CI], 0.79-0.97; p=0.01), the composite of cardiovascular mortality or hospitalizations for heart failure (HHF HR, 0.71; 95% CI, 0.65-0.78; p<0.001), cardiovascular mortality (HR, 0.86; 95% CI, 0.76-0.98; p=0.02), HHF (HR, 0.62; 95% CI, 0.55-0.71; p<0.001), major adverse cardiovascular events (HR, 0.85; 95% CI, 0.77-0.94; p=0.002), stroke (HR, 0.76; 95% CI, 0.59-0.97; p=0.03), and myocardial infarction (HR, 0.78; 95% CI, 0.67-0.91; p=0.001). These findings were consistent over strata of eGFR, albeit with a lower incidence of stroke in patients treated with SGLT2i with eGFR <45 mL/min/1.73 m² (p-value for interaction=0.04).

CONCLUSIONS:

Compared with a placebo, patients with T2DM and CKD treated with SGLT2i experience a reduction in all-cause mortality, cardiovascular mortality, and HHF. TRIAL REGISTRATION PROSPERO Identifier CRD42023401081.
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