Cardiometabolic & kidneySecondary analysis

Effects of Semaglutide on Heart Failure Outcomes in Diabetes and Chronic Kidney Disease in the FLOW Trial

J Am Coll CardiolPublished

  • Secondary analysis of the FLOW randomised trial
  • prespecified analysis

Heart failure (HF) data collected by the investigator; Cardiovascular (CV) death adjudicated by an independent committee

Authors' conclusion

Semaglutide substantially reduced the risk of time to first composite outcome of HF events or CV death, as well as HF events and CV death alone, in a high-risk population with T2D and CKD.

Study context

Population
People with T2DM and chronic kidney disease (CKD)
Participants
3,533 people
Comparison
Semaglutide vs placebo
Primary endpoint
Composite of:
  • HF events (new onset or worsening HF leading to unscheduled hospital admission or urgent visit, with initiated or intensified diuretic/vasoactive therapy)
  • CV death
Follow-up
Median 3.4 years

Primary result

As reported in the abstract

Hazard ratio

0.73

95% CI 0.62–0.87

P = 0.0005

Semaglutide vs Placebo
HR 0.73 (95% CI 0.62–0.87); P = 0.0005

Further findings

OutcomeHR (95% CI)P value
HF events alone0.73 (0.58–0.92)P = 0.0068
CV death alone0.71 (0.56–0.89)P = 0.0036
Composite HF outcome, by HF at baseline (subgroup) — Semaglutide vs Placebo · with HF at baseline0.73 (0.54–0.98)P = 0.0338
Composite HF outcome, by HF at baseline (subgroup) — Semaglutide vs Placebo · without HF at baseline0.72 (0.58–0.89)P = 0.0028

HF outcomes (HF events or CV death) by NYHA class and HF subtype

Risk generally higher in NYHA class III and HFrEF, regardless of treatment

Original publication

Effects of Semaglutide on Heart Failure Outcomes in Diabetes and Chronic Kidney Disease in the FLOW Trial. J Am Coll Cardiol. Published 30 August 2024. doi:10.1016/j.jacc.2024.08.004

Summarised from the published abstract; every number is checked against it