Cardiac troponin T as a prognostic marker in patients with heart failure : a 3-year outcome study
Mesut Demir1, Mehmet Kanadasi, Onur Akpinar
1Department of Cardiology, Cukurova University, School of Medicine, Adana, Turkey. mdemir@cu.edu.tr
Insights
Elevated cardiac troponin T (cTnT) in congestive heart failure (CHF) patients indicates higher mortality risk. Early identification of worsening CHF may be possible using cTnT levels.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Cardiac troponin T (cTnT) is a specific marker for myocardial cell death.
- Elevated cTnT levels are observed in some congestive heart failure (CHF) patients.
- The association between cTnT release and CHF decompensation requires further investigation.
Purpose of the Study:
- To test if decompensated CHF is linked to increased cTnT release.
- To correlate cTnT levels with patient outcomes in CHF.
- To identify cTnT as a potential predictor of mortality and morbidity in CHF.
Main Methods:
- Studied 55 hospitalized CHF patients (38-86 years).
- Assessed cTnT levels, with >or=0.1 ng/mL considered positive.
- Evaluated left ventricular ejection fraction (EF) via echocardiography.
- Conducted 3-year annual follow-up for mortality and hospital admissions.
Main Results:
- cTnT was positive in 20% of patients.
- cTnT-positive patients had lower EF and higher NYHA classification.
- Mortality rate was significantly higher in cTnT-positive patients (72.7% vs. 38.6%).
- cTnT positivity independently predicted mortality and morbidity.
Conclusions:
- cTnT positivity is an independent risk factor for long-term mortality and morbidity in CHF patients.
- Elevated serum cTnT may help identify patients with worsening CHF.
- This finding supports the use of cTnT for risk stratification in heart failure management.
Abstract:
Cardiac troponin T (cTnT), a highly sensitive and specific indicator of myocardial cell death, may be elevated in congestive heart failure (CHF). The aims of this study were to test the hypothesis that decompensated CHF may be associated with an increase in cTnT release and to correlate between cTnT levels and patient outcomes. The authors studied 55 patients aged between 38 and 86 years (30 women and 25 men) who were hospitalized for CHF. Left ventricular ejection fraction (EF) was calculated by using modified Simpson's rule by echocardiography. cTnT levels were assessed. Troponin T >or=0.1 ng/mL was considered as positive. All patients were contacted by phone annually during the next 3 years, and their history of subsequent hospital admissions and current health status were recorded. cTnT was negative in 44 (80%) and positive in 11 (20%) patients. EF was significantly lower and NYHA was higher in cTnT-positive patients. During the 3-year follow-up period, 25 patients died from CHF. The mortality rate was 8/11 (72.7%) among cTnT-positive patients, whereas the mortality rate was 17/44 (38.6%) among cTnT-negative patients. There were significant relationships among positivity of cTnT, NYHA, EF, and mortality rate. Multivariate regression analysis yielded an independent relationship between positivity of cTnT, NYHA classification, and mortality rate. The percent of hospital admissions due to CHF was also higher in patients with cTnT positive (63.6% versus, 27.3%, p <0.05). In conclusion, this study shows that cTnT positivity is an independent risk factor in predicting the long-term mortality and morbidity rate in patients with CHF. Patients with worsening CHF may possibly be identified early on the basis of their elevated serum cTnT levels.
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