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Published on: November 10, 2021
Cystatin C identifies chronic kidney disease patients at higher risk for complications
Carmen A Peralta1, Ronit Katz, Mark J Sarnak
1San Francisco Veterans Affairs Medical Center, San Francisco, California, USA. carmenalicia.peralta@ucsf.edu
Insights
Cystatin C may help identify patients with chronic kidney disease (CKD) at highest risk for complications. The adverse prognosis for CKD diagnosed by creatinine is mainly seen in those also identified by cystatin C.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Clinical Biomarkers
Background:
- Chronic kidney disease (CKD) diagnosis and prognosis are critical for patient outcomes.
- Creatinine-based estimated glomerular filtration rate (eGFR) is standard, but cystatin C offers a potentially stronger predictor.
- The distinct clinical utility of cystatin C in CKD diagnosis and risk stratification remains unclear.
Purpose of the Study:
- To evaluate the prognostic value of CKD diagnosis using creatinine, cystatin C, or both biomarkers.
- To compare risks for mortality, cardiovascular events, heart failure, and end-stage renal disease (ESRD) based on CKD classification.
Main Methods:
- Analysis of 11,909 participants from the Multi-Ethnic Study of Atherosclerosis (MESA) and Cardiovascular Health Study (CHS).
- CKD diagnosis defined as eGFR <60 ml/min per 1.73 m(2) using CKD-EPI equations for creatinine and cystatin C.
- Participants categorized into mutually exclusive groups: CKD by creatinine only, cystatin C only, both, or neither.
Main Results:
- In MESA, CKD by cystatin C only showed a significantly higher mortality risk (HR 3.23) compared to creatinine only (HR 0.80).
- In CHS, CKD by cystatin C only (HR 1.78) and both (HR 1.74) had higher mortality risks than creatinine only (HR 1.09).
- Similar patterns were observed for cardiovascular disease, heart failure, and kidney failure outcomes, highlighting cystatin C's prognostic role.
Conclusions:
- Adverse prognosis in CKD diagnosed by creatinine is primarily confined to individuals also identified by cystatin C.
- Cystatin C may enhance risk stratification for CKD patients, identifying those at highest risk for adverse events.
- Integrating cystatin C into CKD assessment could refine clinical management and improve patient outcomes.
Abstract:
Although cystatin C is a stronger predictor of clinical outcomes associated with CKD than creatinine, the clinical role for cystatin C is unclear. We included 11,909 participants from the Multi-Ethnic Study of Atherosclerosis (MESA) and the Cardiovascular Health Study (CHS) and assessed risks for death, cardiovascular events, heart failure, and ESRD among persons categorized into mutually exclusive groups on the basis of the biomarkers that supported a diagnosis of CKD (eGFR <60 ml/min per 1.73 m(2)): creatinine only, cystatin C only, both, or neither. We used CKD-EPI equations to estimate GFR from these biomarkers. In MESA, 9% had CKD by the creatinine-based equation only, 2% had CKD by the cystatin C-based equation only, and 4% had CKD by both equations; in CHS, these percentages were 12, 4, and 13%, respectively. Compared with those without CKD, the adjusted hazard ratios (HR) for mortality in MESA were: 0.80 (95% CI 0.50 to 1.26) for CKD by creatinine only; 3.23 (95% CI 1.84 to 5.67) for CKD by cystatin C only; and 1.93 (95% CI 1.27 to 2.92) for CKD by both; in CHS, the adjusted HR were 1.09 (95% CI 0.98 to 1.21), 1.78 (95% CI 1.53 to 2.08), and 1.74 (95% CI 1.58 to 1.93), respectively. The pattern was similar for cardiovascular disease (CVD), heart failure, and kidney failure outcomes. In conclusion, among adults diagnosed with CKD using the creatinine-based CKD-EPI equation, the adverse prognosis is limited to the subset who also have CKD according to the cystatin C-based equation. Cystatin C may have a role in identifying persons with CKD who have the highest risk for complications.
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