Cardiovascular biomarkers as predictors of adverse outcomes in chronic Chagas cardiomyopathy

Chronic Chagas Cardiomyopathy (CCM) is a unique form of cardiomyopathy compared to other etiologies of heart failure. In CCM, risk prediction based on biomarkers has not been well-studied. We assessed the prognostic value of a biomarker panel to predict a composite outcome (CO), including the need f...

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Published inPloS one Vol. 16; no. 10; p. e0258622
Main Authors Echeverría, Luis E, Rojas, Lyda Z, Gómez-Ochoa, Sergio Alejandro, Rueda-Ochoa, Oscar L, Sosa-Vesga, Cristian David, Muka, Taulant, Januzzi, James L, Marcus, Rachel, Morillo, Carlos A
Format Journal Article
LanguageEnglish
Published San Francisco Public Library of Science 28.10.2021
Public Library of Science (PLoS)
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Summary:Chronic Chagas Cardiomyopathy (CCM) is a unique form of cardiomyopathy compared to other etiologies of heart failure. In CCM, risk prediction based on biomarkers has not been well-studied. We assessed the prognostic value of a biomarker panel to predict a composite outcome (CO), including the need for heart transplantation, use of left ventricular assist devices, and mortality. During a median follow-up of 52 months, the mortality rate was 20%, while the CO was observed in 25% of the patients. Four biomarkers (NT-proBNP, hs-cTnT, sST2, and Cys-C) were associated with the CO; concentrations of NT-proBNP and hs-cTnT were associated with the highest AUC (85.1 and 85.8, respectively). Combining these two biomarkers above their selected cut-off values significantly increased risk for the CO (HR 3.18; 95%CI 1.31-7.79). No events were reported in the patients in whom the two biomarkers were under the cut-off values, and when both levels were above cut-off values, the CO was observed in 60.71%. The combination of NT-proBNP and hs-TnT above their selected cut-off values is associated with a 3-fold increase in the risk of the composite outcome among CCM patients. The use of cardiac biomarkers may improve prognostic evaluation of patients with CCM.
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Competing Interests: Dr. Januzzi is a Trustee of the American College of Cardiology, has received grant support from Novartis Pharmaceuticals, Roche Diagnostics, Abbott, Singulex and Prevencio, consulting income from Abbott, Janssen, Novartis, Pfizer, Merck, and Roche Diagnostics, ownership in Imbria Pharmaceuticals, and participates in clinical endpoint committees/data safety monitoring boards for Abbott, AbbVie, Amgen, Boehringer- Ingelheim, Janssen, and Takeda. This does not alter our adherence to PLOS ONE policies on sharing data and materials. The other authors have no conflict of interests to declare.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0258622