Sacubitril/valsartan and cardiovascular biomarkers among patients with recent COVID-19 infection: The PARACOR-19 randomized clinical trial

Eur J Heart Fail. 2024 Jun;26(6):1393-1398. doi: 10.1002/ejhf.3199. Epub 2024 May 11.

Abstract

Aims: The PARACOR-19 randomized controlled trial (RCT) was designed to examine the effects of sacubitril/valsartan on markers of cardiac injury, inflammation, structure, and function among patients who have recovered from acute coronavirus disease 2019 (COVID-19) infection.

Methods and results: PARACOR-19 was a single-centre, double-blind RCT of patients with cardiovascular risk factors and a history of COVID-19 infection 4-16 weeks prior to enrolment. Patients were randomized to sacubitril/valsartan (titrated to the maximum dose of 97/103 mg twice daily) versus matching placebo. Co-primary endpoints were change from baseline to 12 weeks in high-sensitivity cardiac troponin T (hs-cTnT) and soluble ST2 (sST2). Exploratory endpoints included change from baseline to 12 weeks in additional circulating biomarkers. Overall, 42 patients were randomized between August 2021 and March 2023 (n = 20 sacubitril/valsartan, n = 22 placebo). Median (25th-75th) time from COVID-19 diagnosis to enrolment was 67 (48-80) days. Median age was 67 (62-71) years, 48% were female, and 91% were White. Compared with placebo, sacubitril/valsartan did not have a significant effect on the co-primary endpoints of change from baseline in hs-TnT and sST2 (all p ≥ 0.29). In exploratory analyses, sacubitril/valsartan led to a 46% greater reduction in N-terminal pro-B-type natriuretic peptide (NT-proBNP) and 51% greater reduction in C-terminal telopeptide of collagen type I (CITP). Permanent drug discontinuation occurred in four patients in the sacubitril/valsartan group and three patients in the placebo group. There were no deaths and one patient was hospitalized in each group.

Conclusion: In this pilot RCT of patients who recovered from acute COVID-19, sacubitril/valsartan did not lower hs-cTnT or sST2 compared with placebo. Exploratory analyses suggested potential benefits of sacubitril/valsartan on cardiac wall stress and collagen turnover as measured by NT-proBNP and CITP. Sacubitril/valsartan was well tolerated.

Clinical trial registration: ClinicalTrials.gov NCT04883528.

Keywords: Biomarkers; COVID‐19; Sacubitril/valsartan.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Aminobutyrates* / therapeutic use
  • Angiotensin Receptor Antagonists* / therapeutic use
  • Biomarkers* / blood
  • Biphenyl Compounds*
  • COVID-19 Drug Treatment
  • COVID-19* / blood
  • COVID-19* / complications
  • Double-Blind Method
  • Drug Combinations*
  • Female
  • Heart Failure* / blood
  • Heart Failure* / drug therapy
  • Humans
  • Interleukin-1 Receptor-Like 1 Protein / blood
  • Male
  • Middle Aged
  • Natriuretic Peptide, Brain / blood
  • Peptide Fragments* / blood
  • SARS-CoV-2
  • Tetrazoles / administration & dosage
  • Tetrazoles / therapeutic use
  • Troponin T / blood
  • Valsartan*

Substances

  • Biphenyl Compounds
  • Aminobutyrates
  • Valsartan
  • Drug Combinations
  • sacubitril and valsartan sodium hydrate drug combination
  • Biomarkers
  • Angiotensin Receptor Antagonists
  • Peptide Fragments
  • pro-brain natriuretic peptide (1-76)
  • Tetrazoles
  • Natriuretic Peptide, Brain
  • Troponin T
  • Interleukin-1 Receptor-Like 1 Protein
  • IL1RL1 protein, human

Associated data

  • ClinicalTrials.gov/NCT04883528