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Diagnostic and prognostic value of cystatin C in acute heart failure
Tobias Breidthardt1, Zaid Sabti2, Ronny Ziller3
1Department of Internal Medicine, University of Basel, Switzerland; Cardiovascular Research Institute Basel (CRIB), University of Basel, Switzerland.
Insights
Cystatin C does not reliably predict acute kidney injury (AKI) in acute heart failure (AHF) patients. However, it independently predicts mortality, especially when combined with BNP levels.
Area of Science:
- Nephrology
- Cardiology
- Biomarker Research
Background:
- Accurate early diagnosis of acute kidney injury (AKI) in acute heart failure (AHF) patients remains a clinical challenge.
- Cystatin C is being investigated as a potential early biomarker for AKI detection.
Purpose of the Study:
- To evaluate the diagnostic accuracy of Cystatin C for predicting AKI in AHF patients.
- To assess Cystatin C's role in predicting long-term mortality in this population.
Main Methods:
- 207 AHF patients were enrolled, with plasma Cystatin C measured at presentation and serially.
- Diagnostic accuracy for AKI and prediction of mortality were assessed as primary and secondary endpoints, respectively.
- Creatinine and Cystatin C levels were compared between AKI and Non-AKI groups.
Main Results:
- Cystatin C and creatinine levels were significantly higher in AKI patients compared to Non-AKI patients at presentation.
- The diagnostic accuracy of Cystatin C for AKI was comparable to creatinine but mediocre (AUC 0.67 vs. 0.68).
- Cystatin C levels were higher in non-survivors and independently predicted mortality, particularly when combined with BNP.
Conclusions:
- Plasma Cystatin C is not an adequate predictor of AKI in AHF patients.
- Cystatin C independently predicts mortality in AHF patients, even after adjusting for renal function and other factors.
- Combining Cystatin C with BNP may improve mortality prediction in AHF.
Background:
The accurate early diagnosis of acute kidney injury (AKI) in patients with acute heart failure (AHF) is an unmet clinical need. Cystatin C might improve the early detection of AKI.
Methods:
207 patients presenting to the emergency department with AHF were enrolled. Cystatin C was measured in plasma in a blinded fashion at presentation and serially thereafter. The potential of Cystatin C levels to predict AKI was assessed as the primary endpoint. Long-term mortality was assessed as a secondary endpoint.
Results:
At presentation, creatinine (140μmol/L [91-203] vs. 97μmol/L [76-132], p<0.01) and Cystatin C (2.00mg/L [1.30-3.08] vs. 1.45mg/L [1.00-1.90], p<0.01) levels were significantly higher in AKI compared to Non-AKI patients. The diagnostic accuracy for AKI quantified by the area under the receiver operating characteristic curve was mediocre and comparable for both markers (creatinine 0.68; 95%CI 0.58-78 vs. Cystatin C 0.67; 95%CI 0.58-0.76). Serial measurements of Cystatin C did not further increase the prognostic accuracy for AKI. Cystatin C levels were significantly higher in decedents than in survivors (1.90mg/L [1.30-2.70] vs. 1.30mg/L [1.0-1.6], p<0.001). The combination of Cystatin C and BNP levels significantly improved the prediction of mortality provided by either parameter alone. In multivariable regression analysis Cystatin C remained independently associated with mortality (HR 1.41; 95%CI 1.02-1.95).
Conclusion:
Plasma Cystatin C levels do not adequately predict AKI in patients with AHF. However, in multivariable regression analysis Cystatin C predicted mortality after the adjustment for baseline renal function, AKI, BNP levels and heart failure risk factors.
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