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Association Between Cystatin C and Cardiac Function and Long-Term Prognosis in Patients with Chronic Heart Failure
Xilin Wu1, Ge Xu2, Shiming Zhang1
1Department of Cardiology, First Affiliated Hospital of Guangxi University of Science and Technology, Liuzhou, Guangxi, China (mainland).
Insights
Elevated cystatin C levels in chronic heart failure (CHF) patients correlate with poorer cardiac function and increased 5-year mortality risk. Cystatin C serves as a valuable biomarker for assessing long-term prognosis in CHF.
Area of Science:
- Cardiology
- Biomarkers
- Prognostics
Background:
- Chronic heart failure (CHF) presents significant long-term mortality challenges.
- Identifying reliable biomarkers for prognosis in CHF is crucial for patient management.
Purpose of the Study:
- To investigate the association between cystatin C levels and cardiac function in CHF patients.
- To evaluate the relationship between cystatin C and long-term all-cause mortality in CHF.
Main Methods:
- 418 CHF patients were stratified into three groups based on cystatin C levels.
- Cardiac function (NYHA class) and NT-ProBNP levels were assessed.
- A 5-year follow-up was conducted to determine all-cause mortality rates.
Main Results:
- Higher cystatin C and NT-ProBNP levels were observed in patients with advanced cardiac dysfunction (NYHA class IV).
- A significant positive correlation was found between cystatin C and NT-ProBNP.
- Elevated cystatin C levels (Quantile 3) were independently associated with increased 5-year all-cause mortality (OR=1.71, P=0.034).
Conclusions:
- Cystatin C is positively correlated with cardiac function and NT-ProBNP in CHF patients.
- Cystatin C demonstrates potential as a serological marker for predicting long-term prognosis in chronic heart failure.
Abstract:
BACKGROUND The aim of this study was to investigate the association between cystatin C and cardiac function and long-term prognosis in patients with chronic heart failure (CHF). MATERIAL AND METHODS We selected 418 CHF patients admitted to our hospital as subjects. Patients were divided into 3 groups according to the cystatin C level (Quantile 1 group: 0.65-1.04 mg/L, Quantile 2 group: 1.05-1.35 mg/L, and Quantile 3 group: 1.36-7.84 mg/L), and patients were followed up for 5 years. We used odds ratio (OR) and 95% confidence interval (CI) to compare the results. RESULTS The cystatin C and NT-ProBNP level in the cardiac function grade (NYHA) class IV group were higher than those in the class III group (P<0.05). Pearson correlation analysis showed that there was a positive correlation between cystatin C and NT-ProBNP log₁₀ transform in CHF patients (r=0.411). During 5-year follow-up, 231 patients died and the 5-year all-cause mortality rate was 55.26% (231/418). There was a significant difference in 5-year all-cause mortality among the 3 groups (P for trend=0.010). After adjusting for potential confounders by multivariate regression analysis, the Quantile 2 group vs. Quantile 1 group were OR=0.83, 95% CI 0.51 to 1.35, P=0.448, and the Quantile 3 group vs. Quantile 1 group were OR=1.71, 95% CI. 1.04 to 2.82, P=0.034. Curve fitting showed that cystatin C was positively correlated with 5-year all-cause mortality in CHF patients. CONCLUSIONS Cystatin C was positively correlated with cardiac function and NT-ProBNP in CHF patients. Cystatin C could be used as a serological index to evaluate the long-term prognosis of CHF patients.
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