Heart failure & cardiomyopathies

Effects of SGLT2 inhibition on incident heart failure in carriers of cardiomyopathy-associated genetic variants

Nat MedPublished Secondary analysis of the DECLARE-TIMI 58 randomised trial

Study context

Population
Adults with T2DM and increased CV risk with sequence data; carriers vs noncarriers of P/LP variants in high-confidence cardiomyopathy genes121 carriers
Participants
12,685 adults
Comparison
Dapagliflozin vs placebo in carriers vs noncarriers of cardiomyopathy variants
Primary endpoint
Hospitalization for HF (HHF)
Follow-up
Median 4.2 years
Methodological detailswhole-exome sequencing, genetic subgroup analysis
  • Whole-exome sequencing
  • Genetic subgroup analysis

Primary result

As reported in the abstract

HHF, by cardiomyopathy variant carrier status · median 4.2 years
Dapagliflozin vs PlaceboHazard ratio (95% CI)
Carriers
0.18(0.04–0.86)
Noncarriers
0.70(0.57–0.86)
Absolute risk reduction, carriers
13.0%
Absolute risk reduction, noncarriers
1.0%

Further findings

Hospitalization for HF (HHF) absolute risk reduction, no prior heart failure (HF) (subgroup)

Absolute risk reduction, carriers without prior HF
12.8%
Absolute risk reduction, noncarriers
0.6%
  • 82% of carriers had no prior HF
  • Interaction P 0.01

Original publication

Effects of SGLT2 inhibition on incident heart failure in carriers of cardiomyopathy-associated genetic variants. Nat Med. Published 8 June 2026. doi:10.1038/s41591-026-04439-x

Composed by AI from the published abstract and checked against it. How Briefs are made →

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