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Multimarker strategy for the prediction of 6-month major adverse cardiac events in patients with and without congestive heart failure after acute myocardial infarction
경북대학교병원 순환기 내과
이장훈, 채성철, 박선희, 강정규, 김나영, 양동헌, 박헌식, 조용근, 전재은, 박의현
Background: The aim of this study was to investigate the combined prognostic value of admission serum levels of N-terminal pro-B type natriuretic peptide (NT-proBNP), cardiac troponin I, uric acid (UA), and high sensitivity C-reactive protein (hs-CRP) on 6-month major adverse cardiac events (MACE) in patients with and without congestive heart failure (CHF) after acute myocardial infarction (AMI). Methods: Between November 2005 and February 2010, 1,804 patients (1,231 men; mean age = 64.3 ± 11.9 years-old) were followed up more than 6-month after their AMI and finally analyzed in this study. The 6-month MACEs were defined as death, MI, and revascularizations. Results: Overall, patients with CHF (Killip class II-IV) were present in 461 (25.6%). The 6-month MACEs were significantly higher in CHF patients compared with no-CHF patients (7.1% versus 26.7%, p <0.001). In no-CHF patients, the levels of log-transformed NT-proBNP (p<0.001) and hs-CRP (p<0.001) were significantly higher in patients with MACEs, whereas the levels of log-transformed NT-proBNP (p<0.001), hs-CRP (p<0.001), and UA (p<0.001) were significantly higher in patients with MACEs in CHF patients. In Cox proportional hazards model, elevated serum levels of NT-pro BNP (hazard ratio [HR] 1.422, 95% confidence interval [CI] 1.133-1.785, p =0.002) was the only independent predictor of 6-month MACE in CHF patients, whereas elevated serum levels of NT-pro BNP (HR 1.348, 95% CI 1.032-1.760, p =0.028) and UA (HR 1.181, 95% CI 1.028-1.357, p =0.018) were independent predictors of 6-month MACE after adjustment for confounding variables. When the patients were divided into 4 groups according to the number of elevated biomarkers (NT-proBNP, UA, hs-CRP) in CHF patients, there was a significant gradual increased risk of 6-month MACE with increasing in the number of elevated biomarkers (9.5%, 16.9%, 30.5% and 44.9% of patients with 0, 1, 2 and 3 elevated biomarkers respectively, p <0.001). In Cox proportional hazards model, patients with 2 (HR 2.932, 95% CI 1.149-7.485, p =0.024) and 3 (HR 4.153, 95% CI 1.506-11.452, p =0.006) elevated biomarkers had significantly higher 6-month MACEs compared with patients with 0 elevated biomarkers. Conclusion: Biomarkers are differently related to 6-months MACEs in post-MI patients. With increasing number of elevated biomarkers, the risk of 6-month MACEs increases gradually that implies treatment intensification, and closer follow-up, particularly in CHF patients.


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