Why the study?
NT-proBNP, cTnT, and sST2 provide complementary prognostic information in HFrEF, but their changes needed evaluation regarding associations with changes in cardiac structure, function, and health status.
Are changes in cardiac biomarkers (NT-proBNP, cTnT, sST2) associated with alterations in cardiac structure, function, and health status in patients with HFrEF?
Are changes in cardiac biomarkers (NT-proBNP, cTnT, sST2) associated with alterations in cardiac structure, function, and health status in patients with HFrEF?
In patients with HFrEF, reductions in NT-proBNP correlate with improvements in cardiac structure, function, and health status, highlighting the complementary pathophysiologic implications of different cardiac biomarkers.
NT-proBNP changes may track remodeling and health status gains in HFrEF; leaves open surrogate validation in prospective trials.
AIMS: N-terminal pro-B-type natriuretic peptide (NT-proBNP), cardiac troponin T (cTnT) and soluble ST2 (sST2) provide complementary prognostic information in heart failure with reduced ejection fraction (HFrEF). We aimed to assess the association between changes in these markers with changes in cardiac structure, function and health status. METHODS AND RESULTS: Patients in the EVALUATE-HF trial (n = 464) were randomized to sacubitril/valsartan or enalapril for 12 weeks, followed by 12-week open-label sacubitril/valsartan. Cardiac biomarkers, echocardiography, and Kansas City Cardiomyopathy Questionnaires (KCCQ) were completed at baseline, and after 12 and 24 weeks. A total of 410 patients (88%) had serial biomarker measurements available (mean age 67 ± 9 years, 75% male and 75% white). After 24 weeks of treatment, NT-proBNP, sST2 and cTnT decreased by median (Q1, Q3) -31% (-55%, +6%), -6% (-19%, +8%) and - 3% (-13%, +8%), respectively (all p < 0.001). Decreases in NT-proBNP were associated with reductions in cardiac volumes and improvements in systolic and diastolic function and health status. Decreases in cTnT were associated with reductions in left ventricular mass, but not with changes in left ventricular function or KCCQ. Decreases in sST2 were consistently associated with improvements in health status, but not with measures of cardiac structure or function. There was no effect modification from treatment on the associations investigated (p for interaction >0.05) CONCLUSION: In HFrEF, serial changes in NT-proBNP correlate with changes in several key measures of cardiac structure and health status. cTnT changes correlate with changes in left ventricular mass and sST2 with changes in health status. These data highlight possible complementary pathophysiologic implications of changes in NT-proBNP, cTnT and sST2. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02874794.
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Myhre et al. (2022) studied this question.
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