<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(10)</volume><submitter>Echeverria LE</submitter><funding>Universität St. Gallen</funding><funding>Departamento Administrativo de Ciencia, Tecnología e Innovación</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>Prospective cohort study of 100 adults with different stages of CCM. Serum concentrations of amino-terminal pro-B type natriuretic peptide (NT-proBNP), galectin-3 (Gal-3), neutrophil gelatinase-associated lipocalin (NGAL), high sensitivity troponin T (hs-cTnT), soluble (sST2), and cystatin-C (Cys-c) were measured. Survival analyses were performed using Cox proportional hazard models.&lt;h4>Results&lt;/h4>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%.&lt;h4>Conclusion&lt;/h4>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.</pubmed_abstract><journal>PloS one</journal><pagination>e0258622</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8553084</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cardiovascular biomarkers as predictors of adverse outcomes in chronic Chagas cardiomyopathy.</pubmed_title><pmcid>PMC8553084</pmcid><pubmed_authors>Gomez-Ochoa SA</pubmed_authors><pubmed_authors>Muka T</pubmed_authors><pubmed_authors>Marcus R</pubmed_authors><pubmed_authors>Echeverria LE</pubmed_authors><pubmed_authors>Rojas LZ</pubmed_authors><pubmed_authors>Januzzi JL</pubmed_authors><pubmed_authors>Rueda-Ochoa OL</pubmed_authors><pubmed_authors>Sosa-Vesga CD</pubmed_authors><pubmed_authors>Morillo CA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cardiovascular biomarkers as predictors of adverse outcomes in chronic Chagas cardiomyopathy.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>Prospective cohort study of 100 adults with different stages of CCM. Serum concentrations of amino-terminal pro-B type natriuretic peptide (NT-proBNP), galectin-3 (Gal-3), neutrophil gelatinase-associated lipocalin (NGAL), high sensitivity troponin T (hs-cTnT), soluble (sST2), and cystatin-C (Cys-c) were measured. Survival analyses were performed using Cox proportional hazard models.&lt;h4>Results&lt;/h4>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%.&lt;h4>Conclusion&lt;/h4>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.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-04-04T13:50:39.325Z</modification><creation>2025-04-04T13:50:39.325Z</creation></dates><accession>S-EPMC8553084</accession><cross_references><pubmed>34710112</pubmed><doi>10.1371/journal.pone.0258622</doi></cross_references></HashMap>