Heart failure & cardiomyopathiesSecondary analysis

End-organ Protective Effect of Serelaxin in Patients Hospitalized for Heart Failure: Results of the Biomarker Substudy of Relaxin in Acute Heart Failure-2 (RELAX-AHF-2)

Eur J Heart FailPublished

  • Secondary analysis of the RELAX-AHF-2 randomised trial
  • biomarker substudy
  • pre-specified

Authors' conclusion

In this substudy, serelaxin decreased plasma concentrations of cardiac, renal and hepatic injury markers. Changes of most of these markers were associated with cardiovascular mortality. In this pre-specified biomarker subgroup, serelaxin did not reduce 180-day cardiovascular mortality but significantly reduced worsening heart failure through day 5.

Study context

Population
Patients enrolled within 16 h of presentation for HF hospitalizationof 6545 in RELAX-AHF-2
Participants
1,020 patients
Comparison
Serelaxin vs placebo
Primary endpoint
Percentage change from baseline in organ damage-related biomarkers

Primary result

As reported in the abstract

Percentage change from baseline in biomarkers
GroupTroponin T through day 14Creatinine at day 2Cystatin C at day 2Uric acid at day 2NT-proBNP to day 2
Serelaxin+0.2%−0.8%+3.8%+0.8%−39.8%
Placebo+40.3%+5.8%+8.3%+7.2%−27.6%
  • Serelaxin vs Placebo: P = 0.042 — troponin T
  • Serelaxin vs Placebo: P = 0.002 — creatinine
  • Serelaxin vs Placebo: P = 0.016 — cystatin C
  • Serelaxin vs Placebo: P = 0.0014 — uric acid
  • Serelaxin vs Placebo: P = 0.002 — NT-proBNP

Further findings

OutcomeHR (95% CI)P value
CV death · 180 days0.78 (0.49–1.25)P = 0.30
Worsening HF · through day 50.55 (0.33–0.93)P = 0.027

Association of early biomarker changes with 180-day mortality

Early changes in NT-proBNP and troponin, but not creatinine, cystatin C and uric acid, associated with 180-day mortality

Original publication

End-organ Protective Effect of Serelaxin in Patients Hospitalized for Heart Failure: Results of the Biomarker Substudy of Relaxin in Acute Heart Failure-2 (RELAX-AHF-2). Eur J Heart Fail. Published 12 December 2024. doi:10.1002/ejhf.3551

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