TY - JOUR
T1 - High levels of troponin T are associated with ventricular remodeling and adverse in-hospital outcome in heart failure
AU - Perna, Eduardo Roque
AU - Macín, Stella Maris
AU - Canella, Juan Pablo Cimbaro
AU - Alvarenga, Pablo Marcelo
AU - Pantich, Rolando Esteban
AU - Ríos, Nelson Gerardo
AU - Cialzeta, Jorge Raúl
AU - Farías, Eduardo Francisco
AU - Badaracco, Jorge Reynaldo
AU - Brizuela, Monica
AU - Jantus, Eloísa
AU - Missov, Emil D.
PY - 2004/3
Y1 - 2004/3
N2 - Background: Heart failure progression is associated with ventricular remodeling and ongoing myofibrillar degradation. We hypothesized that myocardial damage, detected by high levels of troponin T, would correlate with echocardiographic measurements of left ventricular remodeling and worse in-hospital course in decompensated heart failure. Material/Methods: 159 patients with decompensated heart failure without acute coronary event were included. A troponin T value ≥0.2 ng/ml in samples taken 6, 12 or 24 hours after admission was considered abnormal. Results: High troponin T levels were identified in 24 patients (15%) (Group 1). Mean age for group 1 was 65.9 vs. 63.7 years in patients with troponin T<0.2 (Group 2) (p=ns). Ischemic etiology in groups 1 and 2 was found in 58.3 and 38.5% (p=0.07). Two-dimensional echocardiograms in groups 1 and 2 revealed higher left ventricular diameters, diastolic (61.7± 10 vs. 56.9± 10.3 mm, p=0.041) as well as systolic (49.4±13.5 vs. 42.0±12.0 mm, p=0.019), and lower ejection fraction (30.1±14 vs. 39.0±17.7%, p=0.03). Incidence of combined end point of death or refractory heart failure was 20.8 and 3.7% in groups 1 and 2 (p=0.007; OR=6.8; CI95%=1.5-31.2). In a multiple regression model, a history of infarction and chronic obstructive puhnonary disease, tissue hypoperfusion, radiographic pulmonary edema, and high troponin T levels emerged as the independent predictors. Conclusions. High troponin T levels were found in 15% of patients with acute exacerbation of heart failure; this finding was independently associated with worse prognosis. Echocardiograms suggested that more severe ventricular remodeling is one subjacent mechanism related with biochemically detected myocardial injury in this setting.
AB - Background: Heart failure progression is associated with ventricular remodeling and ongoing myofibrillar degradation. We hypothesized that myocardial damage, detected by high levels of troponin T, would correlate with echocardiographic measurements of left ventricular remodeling and worse in-hospital course in decompensated heart failure. Material/Methods: 159 patients with decompensated heart failure without acute coronary event were included. A troponin T value ≥0.2 ng/ml in samples taken 6, 12 or 24 hours after admission was considered abnormal. Results: High troponin T levels were identified in 24 patients (15%) (Group 1). Mean age for group 1 was 65.9 vs. 63.7 years in patients with troponin T<0.2 (Group 2) (p=ns). Ischemic etiology in groups 1 and 2 was found in 58.3 and 38.5% (p=0.07). Two-dimensional echocardiograms in groups 1 and 2 revealed higher left ventricular diameters, diastolic (61.7± 10 vs. 56.9± 10.3 mm, p=0.041) as well as systolic (49.4±13.5 vs. 42.0±12.0 mm, p=0.019), and lower ejection fraction (30.1±14 vs. 39.0±17.7%, p=0.03). Incidence of combined end point of death or refractory heart failure was 20.8 and 3.7% in groups 1 and 2 (p=0.007; OR=6.8; CI95%=1.5-31.2). In a multiple regression model, a history of infarction and chronic obstructive puhnonary disease, tissue hypoperfusion, radiographic pulmonary edema, and high troponin T levels emerged as the independent predictors. Conclusions. High troponin T levels were found in 15% of patients with acute exacerbation of heart failure; this finding was independently associated with worse prognosis. Echocardiograms suggested that more severe ventricular remodeling is one subjacent mechanism related with biochemically detected myocardial injury in this setting.
KW - Decompensated heart failure
KW - Prognosis
KW - Troponin T
KW - Ventricular remodeling
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M3 - Article
C2 - 14976458
AN - SCOPUS:12144287676
SN - 1234-1010
VL - 10
SP - CR90-CR95
JO - Medical Science Monitor
JF - Medical Science Monitor
IS - 3
ER -