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Cystatin C-Based Renal Function in Predicting the Long-Term Outcomes of Chronic Total Occlusion After Percutaneous
Bolin Li1, Jie Rong2, Bobo Wang3
1Department of Cardiology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Insights
Serum cystatin C-based estimated glomerular filtration rate (eGFR) better predicts adverse cardiovascular events and mortality in patients undergoing percutaneous coronary intervention (PCI) for chronic total occlusion (CTO) compared to creatinine-based eGFR.
Area of Science:
- Cardiology
- Nephrology
- Biomarkers
Background:
- Assessing renal function is crucial for predicting cardiovascular events in patients with chronic total occlusion (CTO) undergoing percutaneous coronary intervention (PCI).
- Existing creatinine-based estimates of kidney function may not fully capture renal status in this population.
- The predictive value of cystatin C-based estimated glomerular filtration rate (eGFR) for adverse outcomes in CTO PCI patients requires further investigation.
Purpose of the Study:
- To compare the predictive performance of serum cystatin C-based eGFR against multiple creatinine-based eGFR equations for adverse cardiovascular events in patients with CTO undergoing PCI.
- To determine if cystatin C-based eGFR offers improved prognostic value for all-cause mortality and cardiac death.
Main Methods:
- Retrospective study including 671 patients who underwent CTO PCI.
- Calculated eGFR using modification of diet in renal disease (cMDRD) and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations.
- Categorized patients into KDIGO kidney stages based on eGFR and analyzed primary (all-cause mortality) and secondary (cardiac death) endpoints.
Main Results:
- Serum cystatin C-based eGFR demonstrated superior predictive performance, indicated by a larger area under the receiver operating characteristic (ROC) curve for both all-cause mortality (0.73) and cardiac death (0.73).
- Cystatin C-based eGFR showed the highest prognostic value for all-cause mortality (adjusted HR 3.6) and cardiac death (adjusted HR 2.9) compared to other formulas.
- Cystatin C-based eGFR significantly improved risk reclassification, evidenced by high net reclassification improvement and integrated discrimination improvement.
Conclusions:
- Serum cystatin C-based eGFR is a more effective predictor of all-cause mortality and cardiac death than traditional creatinine-based equations in patients with CTO undergoing PCI.
- This finding highlights the potential clinical utility of cystatin C-based eGFR for risk stratification in this high-risk cardiovascular patient group.
Abstract:
Renal function estimated by various biomarkers predicting for adverse cardiovascular events has not been well-identified in received percutaneous coronary intervention (PCI) for chronic total occlusion (CTO), the advanced stages of atherosclerosis. We aim to determine whether the serum cystatin C-based-estimated glomerular filtration rate (eGFR) can have an improved predictive value in patients with CTO lesions undergoing PCI as compared with multiple creatinine-based estimates of kidney function. Six hundred and seventy-one patients received CTO PCI were retrospectively included in the study. The eGFR was calculated by modification of diet in renal disease equation for Chinese (cMDRD) and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations at baseline, respectively. Then, the cohort was categorized into three groups according to standard KDIGO kidney stages based on eGFR. The primary endpoint was all-cause mortality, and the secondary endpoint was cardiac death. Strikingly, cystatin C-based eGFR showed a better performance with the greater area being under the receiver operating characteristic (ROC) curve (0.73 for all-cause mortality and 0.73 for cardiac death, separately) and a better assessment for survival free from adverse event across renal levels among four eGFR equations. Compared with eGFR calculated by other formulas, serum cystatin C-based eGFR showed the highest prognostic value for both all-cause mortality (adjusted HR 3.6, 95% CI 1.6-8.1, P = 0.002) and cardiac death (adjusted HR 2.9, 95% CI 1.0-8.1, P = 0.028). Moreover, cystatin C-based eGFR significantly improved the risk reclassification of event with a high value of net reclassification improvement and integrated discrimination improvement. This study may prove that cystatin C-based eGFR is a better predictor of both all-cause mortality and cardiac death than other equations in populations with CTO undergoing PCI.
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