← SGLT2 inhibitors × cardiovascular events

TrialThe New England journal of medicine2019

Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy.

Vlado Perkovic et al.PubMed ↗Publisher ↗

The primary results report of NCT02065791. Its numbers are set against the trial’s posted results below.

  • Canagliflozinlooks good hereLower renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes, fewer cardiovascular death, myocardial infarction, or stroke, lower hospitalization for heart failure.Randomised, large.

What the trial testedrandomised · 4,401 people · 2019

Randomised vs placebo

Lowered renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes

Doesn’t vote: same as the registry's posted result, which counts instead

−34%−47% to −19%

canagliflozin vs placebo

Bigger than 8 in 10 for cardiovascular events

As reported

HR 0.66, 95% CI 0.53–0.81

Randomised vs placebo

Reduced cardiovascular death, myocardial infarction, or stroke

Doesn’t vote: same as the registry's posted result, which counts instead

−20%−33% to −5%

canagliflozin vs placebo

Bigger than 4 in 10 for cardiovascular events

As reported

HR 0.80, 95% CI 0.67–0.95

Randomised vs placebo

Lowered hospitalization for heart failure

Doesn’t vote: same as the registry's posted result, which counts instead

−39%−53% to −20%

canagliflozin vs placebo

Bigger than 8 in 10 for cardiovascular events

As reported

HR 0.61, 95% CI 0.47–0.80

Not counted

Lowered end-stage kidney disease

−32%−46% to −14%

canagliflozin vs placebo

Bigger than 7 in 10 on the map

As reported

HR 0.68, 95% CI 0.54–0.86

Against the trial’s posted results

  • Same as the trial’s posted resultThis paper HR 0.61 (0.47–0.80)Posted HR 0.61 (0.47–0.80), p = 0.0003Hospitalized Heart Failure (HHF)
  • Same as the trial’s posted resultThis paper HR 0.80 (0.67–0.95)Posted HR 0.80 (0.67–0.95), p = 0.0121Major Adverse Cardiac Event (MACE)
  • Same as the trial’s posted resultThis paper HR 0.70 (0.59–0.82)Posted, primary outcome HR 0.70 (0.59–0.82), p < 0.0001Primary Composite Endpoint of Doubling of Serum Creatinine (DoSC), End-stage Kidney Disease (ESKD), and Renal or Cardiovascular (CV) Death
  • Same as the trial’s posted resultThis paper HR 0.66 (0.53–0.81)Posted HR 0.66 (0.53–0.81), p <0.0001Renal Composite Endpoint

Who was studied, and how

4,401people with cardiovascular disease, in this paper

The trial randomly assignedassigned by chance

canagliflozin
placebo

Lowered renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes−34%

Reduced cardiovascular death, myocardial infarction, or stroke−20%

Lowered hospitalization for heart failure−39%

randomised

the abstract, start to end

… causes was lower by 34% (hazard ratio, 0.66; 95% CI, 0.53 to 0.81; P<0.001), and the relative risk of end-stage kidney disease was lower by 32% (hazard ratio, 0.68; 95% CI, 0.54 to 0.86; …

… infarction, or stroke (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P = 0.01) and hospitalization for heart failure (hazard ratio, 0.61; 95% CI, 0.47 to 0.80; …

← favours treatmentfavours comparator →
could be chance
Renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causescanagliflozin vs placebo
HR 0.660.53–0.81
End-stage kidney diseasecanagliflozin vs placebo
HR 0.680.54–0.86
Cardiovascular death, myocardial infarction, or strokecanagliflozin vs placebo
HR 0.800.67–0.95
Hospitalization for heart failurecanagliflozin vs placebo
HR 0.610.47–0.80
SGLT2 inhibitorsCardiovascular eventsKidney outcomes
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Full record →Abstract, authors, funding and every citing paper · PMID 30990260