Abstract
Background: New evidence has emerged that the assessment of multiple biomarkers such as cardiac troponin T (cTnT) and N-terminal pro-brain natriuretic peptide (NT-proBNP) in patients with non-ST-elevation acute coronary syndrome (nSTE-ACS) provides unique prognostic information. The purpose of this study was to assess the association between baseline NT-proBNP levels and outcome in patients who have nSTE-ACS with an elevated cTnT and to determine whether patients with elevated NT-proBNP levels benefit from an early invasive treatment strategy. Methods: Baseline samples for NT-proBNP measurements were available in 1141 patients who have nSTE-ACS with an elevated cTnT randomized to an early or a selective invasive strategy. Patients were followed-up for the occurrence of death, myocardial infarction (MI), and rehospitalization for angina. Results: We showed that increased levels of NT-proBNP were associated with several indicators of risk and severe coronary artery disease. Mortality by 1 year was 7.3% in the highest quartile (≥1170 ng/L for men, ≥2150 ng/L for women) compared with 1.1% of patients in the lower 3 quartiles (P < .0001). N-terminal pro-brain natriuretic peptide (highest quartile vs lower 3 quartiles) was a strong independent predictor of mortality (hazard ratio 5.0, 95% CI 2.1-11.6, P = .0002). However, NT-proBNP levels were not associated with the incidence of recurrent MI by 1 year. Furthermore, we could not demonstrate a benefit of an early invasive strategy compared with a selective invasive strategy in patients with an elevated NT-proBNP level. Conclusions: We confirmed that NT-proBNP is a strong independent predictor of mortality by 1 year but not of recurrent MI in patients who have nSTE-ACS with an elevated cTnT. We could not demonstrate a benefit of an early invasive strategy compared with a selective invasive strategy.
Original language | English |
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Pages (from-to) | 485-492 |
Number of pages | 8 |
Journal | American Heart Journal |
Volume | 153 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2007 |
Externally published | Yes |
Bibliographical note
Funding Information:The ICTUS study was supported by the Interuniversitary Cardiology Institute of the Netherlands; the Working Group on Cardiovascular Research of the Netherlands; and educational grants from Eli Lilly (Houten, The Netherlands), Sanofi/Synthelabo (Gouda, The Netherlands), Aventis (Gouda, The Netherlands), Pfizer (Capelle a/d IJsel, The Netherlands), and Medtronic (Heerlan, The Netherlands), Roche Diagnostics (Almere, The Netherlands) kindly provided the reagents for measurements of cardiac troponin T and N-terminal pro–brain natriuretic peptide in the core laboratory.