Key result
Dapagliflozin cuts CV death or worsening heart failure ~29% in HFrEF regardless of CKD status.
Why the study?
Many patients with HFrEF have chronic kidney disease that complicates management and is associated with worse outcomes, necessitating assessment of dapagliflozin's safety and efficacy by kidney function.
Does dapagliflozin reduce cardiovascular death or worsening heart failure in patients with HFrEF regardless of baseline kidney function?
RCT (n=4,742)
Placebo-controlled
Randomized
Does dapagliflozin reduce cardiovascular death or worsening heart failure in patients with HFrEF regardless of baseline kidney function?
Answers are grounded in this paper and cite their sources.
Dapagliflozin provides consistent cardiovascular benefits in HFrEF patients regardless of baseline kidney function and significantly slows the long-term decline in eGFR.
Background: Many patients with heart failure and reduced ejection fraction (HFrEF) have chronic kidney disease that complicates pharmacological management and is associated with worse outcomes. We assessed the safety and efficacy of dapagliflozin in patients with HFrEF, according to baseline kidney function, in the DAPA-HF trial (Dapagliflozin and Prevention of Adverse-outcomes in Heart Failure). We also examined the effect of dapagliflozin on kidney function after randomization. Methods: Patients who have HFrEF with or without type 2 diabetes and an estimated glomerular filtration rate (eGFR) ≥30 mL·min –1 ·1.73 m –2 were enrolled in DAPA-HF. We calculated the incidence of the primary outcome (cardiovascular death or worsening heart failure) according to eGFR category at baseline (<60 and ≥60 mL·min –1 ·1.73 m –2 ) and used eGFR at baseline as a continuous measure, as well. Secondary cardiovascular outcomes and a prespecified composite renal outcome (≥50% sustained decline eGFR, end-stage renal disease, or renal death) were also examined, along with a decline in eGFR over time. Results: Of 4742 patients with a baseline eGFR, 1926 (41%) had eGFR <60 mL·min –1 ·1.73 m –2 . The effect of dapagliflozin on the primary and secondary outcomes did not differ by eGFR category or examining eGFR as a continuous measurement. The hazard ratio (95% CI) for the primary end point in patients with chronic kidney disease was 0.71 (0.59–0.86) versus 0.77 (0.64–0.93) in those with an eGFR ≥60 mL·min –1 ·1.73 m –2 (interaction P =0.54). The composite renal outcome was not reduced by dapagliflozin (hazard ratio=0.71 [95% CI, 0.44–1.16]; P =0.17) but the rate of decline in eGFR between day 14 and 720 was less with dapagliflozin, –1.09 (–1.40 to –0.77) versus placebo –2.85 (–3.17 to –2.53) mL·min –1 ·1.73 m –2 per year ( P <0.001). This was observed in those with and without type 2 diabetes ( P for interaction=0.92). Conclusions: Baseline kidney function did not modify the benefits of dapagliflozin on morbidity and mortality in HFrEF, and dapagliflozin slowed the rate of decline in eGFR, including in patients without diabetes. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03036124.
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Jhund et al. (2020) conducted an RCT in Heart failure with reduced ejection fraction (HFrEF) (n=4,742). Dapagliflozin vs. Placebo was evaluated on Cardiovascular death or worsening heart failure (HR 0.71, 95% CI 0.59-0.86, p=0.54 for interaction). Dapagliflozin reduced cardiovascular death or worsening heart failure consistently in HFrEF patients with (HR 0.71; 95% CI 0.59-0.86) and without (HR 0.77) chronic kidney disease.
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