Adding cardiac troponin T and NT-proBNP to the ARIC HF model improved AUCs by 0.040 in women and 0.057 in men, enhancing heart failure risk prediction.
Does the addition of cTnT and NT-proBNP improve incident heart failure risk prediction in individuals without prevalent heart failure?
9,868 participants without prevalent heart failure from the Atherosclerosis Risk in Communities (ARIC) study
Addition of high-sensitivity cardiac troponin T (cTnT) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) to risk prediction models
Standard risk prediction models (age and race alone, or the ARIC HF model which includes age, race, systolic blood pressure, antihypertensive medication use, current/former smoking, diabetes, body mass index, prevalent coronary heart disease, and heart rate)
Incident heart failure risk prediction (measured by area under the receiver operating characteristic curve [AUC], integrated discrimination improvement, net reclassification improvement [NRI], and model fit) over a mean follow-up of 10.4 yearshard clinical
The addition of high-sensitivity cTnT and NT-proBNP to basic demographic data provides an excellent and easily implementable model for predicting incident heart failure risk.
Tasa de eventos absoluta: 0% vs 0%
BACKGROUND Among the various cardiovascular diseases, heart failure (HF) is projected to have the largest increases in incidence over the coming decades; therefore, improving HF prediction is of significant value. We evaluated whether cardiac troponin T (cTnT) measured with a high-sensitivity assay and N-terminal pro–B-type natriuretic peptide (NT-proBNP), biomarkers strongly associated with incident HF, improve HF risk prediction in the Atherosclerosis Risk in Communities (ARIC) study. METHODS Using sex-specific models, we added cTnT and NT-proBNP to age and race (“laboratory report” model) and to the ARIC HF model (includes age, race, systolic blood pressure, antihypertensive medication use, current/former smoking, diabetes, body mass index, prevalent coronary heart disease, and heart rate) in 9868 participants without prevalent HF; area under the receiver operating characteristic curve (AUC), integrated discrimination improvement, net reclassification improvement (NRI), and model fit were described. RESULTS Over a mean follow-up of 10.4 years, 970 participants developed incident HF. Adding cTnT and NT-proBNP to the ARIC HF model significantly improved all statistical parameters (AUCs increased by 0.040 and 0.057; the continuous NRIs were 50.7% and 54.7% in women and men, respectively). Interestingly, the simpler laboratory report model was statistically no different than the ARIC HF model. CONCLUSIONS cTnT and NT-proBNP have significant value in HF risk prediction. A simple sex-specific model that includes age, race, cTnT, and NT-proBNP (which can be incorporated in a laboratory report) provides a good model, whereas adding cTnT and NT-proBNP to clinical characteristics results in an excellent HF prediction model.
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Nambi et al. (Sat,) reported a other. Adding cardiac troponin T and NT-proBNP to the ARIC HF model improved AUCs by 0.040 in women and 0.057 in men, enhancing heart failure risk prediction.
synapsesocial.com/papers/696a3a7fa14b2bc915cfa3dd — DOI: https://doi.org/10.1373/clinchem.2013.203638
Vijay Nambi
Preventive Cardiology
Xiaoxi Liu
China Academy of Railway Sciences
Lloyd E. Chambless
Preventive Cardiology
Clinical Chemistry
Johns Hopkins University
University of Wisconsin–Madison
University of Minnesota
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