Key result
Sacubitril/valsartan did not significantly improve the co-primary endpoints of change in hs-cTnT and sST2 compared with placebo among patients recovered from acute COVID-19 (all p ≥ 0.29).
Why the study?
The study was designed to examine the effects of sacubitril/valsartan on markers of cardiac injury, inflammation, structure, and function among patients recovered from acute COVID-19 infection.
Does sacubitril/valsartan reduce hs-cTnT and sST2 in patients with cardiovascular risk factors and recent COVID-19 infection?
RCT (n=42)
Double-blind
Randomized
No
Does sacubitril/valsartan reduce hs-cTnT and sST2 in patients with cardiovascular risk factors and recent COVID-19 infection?
In patients recovering from acute COVID-19, sacubitril/valsartan did not significantly lower primary cardiac biomarkers hs-cTnT or sST2 compared with placebo, though it was well tolerated.
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.
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Greene et al. (2024) conducted an RCT in Recent COVID-19 infection with cardiovascular risk factors (n=42). Sacubitril/valsartan vs. Placebo was evaluated on Change from baseline to 12 weeks in high-sensitivity cardiac troponin T (hs-cTnT) and soluble ST2 (sST2) (p=≥0.29). Sacubitril/valsartan did not significantly improve the co-primary endpoints of change in hs-cTnT and sST2 compared with placebo among patients recovered from acute COVID-19 (all p ≥ 0.29).
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