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Eur J Heart Fail ; 26(6): 1393-1398, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38733160

RESUMEN

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.


Asunto(s)
Aminobutiratos , Antagonistas de Receptores de Angiotensina , Biomarcadores , Compuestos de Bifenilo , COVID-19 , Combinación de Medicamentos , Insuficiencia Cardíaca , Fragmentos de Péptidos , Valsartán , Humanos , Aminobutiratos/uso terapéutico , Masculino , Femenino , COVID-19/complicaciones , COVID-19/sangre , Biomarcadores/sangre , Método Doble Ciego , Persona de Mediana Edad , Anciano , Insuficiencia Cardíaca/tratamiento farmacológico , Insuficiencia Cardíaca/sangre , Antagonistas de Receptores de Angiotensina/uso terapéutico , Fragmentos de Péptidos/sangre , Tetrazoles/uso terapéutico , Tetrazoles/administración & dosificación , SARS-CoV-2 , Péptido Natriurético Encefálico/sangre , Troponina T/sangre , Proteína 1 Similar al Receptor de Interleucina-1/sangre , Tratamiento Farmacológico de COVID-19
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