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Plasma level of cardiotrophin-1 as a prognostic predictor in patients with chronic heart failure
Takayoshi Tsutamoto1, Shigeru Asai, Toshinari Tanaka
1Department of Cardiovascular Medicine, Shiga University of Medical Science, Seta-Tsukinowa, Otsu, 520-2192, Japan. tutamoto@belle.shiga-med.ac.jp
Insights
Cardiotrophin-1 (CT-1) and brain natriuretic peptide (BNP) levels predict mortality in chronic heart failure (CHF). Combined CT-1 and BNP measurements offer superior accuracy for predicting CHF patient mortality.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Cardiotrophin-1 (CT-1) is an interleukin-6 (IL-6) family cytokine.
- Elevated CT-1 levels are observed in patients with chronic heart failure (CHF).
Purpose of the Study:
- To investigate the prognostic significance of CT-1 in patients diagnosed with CHF.
- To determine if CT-1 improves mortality prediction in CHF patients.
Main Methods:
- Plasma levels of CT-1, BNP, and IL-6 were measured in 125 CHF patients.
- Patients were followed for a mean of 2.9 years to track mortality.
- Statistical analysis, including stepwise multivariate analysis, was employed.
Main Results:
- CT-1 plasma levels correlated negatively with left ventricular ejection fraction and positively with IL-6.
- Higher CT-1, BNP, and IL-6 levels independently predicted mortality in CHF patients.
- Combined high CT-1 and BNP levels significantly increased mortality risk (HR 2.48).
Conclusions:
- Plasma CT-1 measurement provides valuable prognostic information for CHF.
- Combining CT-1 and BNP levels enhances the accuracy of mortality prediction in CHF patients compared to individual markers.
Background:
Cardiotrophin-1 (CT-1) is a member of the interleukin (IL-6) family of cytokines and is increased in patients with chronic heart failure (CHF).
Aims:
To evaluate the prognostic role of CT-1 in patients with CHF.
Methods And Results:
We measured the plasma levels of CT-1, brain natriuretic peptide (BNP), and IL-6 in 125 patients with CHF. Patients were monitored for a mean follow-up period of 2.9 years. Plasma levels of CT-1 increased with severity of CHF. There was a significant negative correlation between plasma CT-1 and left ventricular ejection fraction. There was a significant correlation between plasma CT-1 and log IL-6. During the follow-up period, 37 patients died. High plasma levels of CT-1, BNP, and IL-6 were independent predictors of mortality on stepwise multivariate analysis. The hazard ratio for mortality in patients with plasma BNP>170 pg/mL and CT-1>658 fmol/mL was 2.48 (95% confidence interval, 1.217-5.060) compared to those with plasma BNP>170 pg/mL and CT-1<658 fmol/mL (p=0.0124).
Conclusion:
These findings indicate that plasma CT-1 measurement provides additional prognostic information and that combined levels of CT-1 and BNP are more accurate at predicting mortality in patients with CHF than either marker alone.
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