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Updated: Jun 12, 2026

A Large Animal Model for Acute Kidney Injury by Temporary Bilateral Renal Artery Occlusion
Published on: February 2, 2021
Plasma cystatin C and acute kidney injury after cardiopulmonary bypass
Ron Wald1, Orfeas Liangos, Mary C Perianayagam
1Division of Nephrology, St. Michael's Hospital and University of Toronto, Toronto, Ontario, Canada. waldr@smh.toronto.on.ca
Insights
Plasma cystatin C (CysC) shows a strong correlation with acute kidney injury (AKI) development after cardiopulmonary bypass (CPB). However, its early diagnostic capability for AKI remains limited.
Area of Science:
- Nephrology
- Cardiology
- Critical Care Medicine
Background:
- Acute kidney injury (AKI) is a significant complication following cardiopulmonary bypass (CPB).
- Early and reliable biomarkers for AKI post-CPB are crucial for timely intervention.
- The utility of plasma cystatin C (CysC) as an AKI marker in this context is not well-established.
Purpose of the Study:
- To evaluate the performance of plasma cystatin C (CysC) in patients undergoing CPB.
- To determine if plasma CysC, measured early post-CPB, can reliably diagnose AKI.
Main Methods:
- A post hoc analysis of 150 patients undergoing CPB.
- Serial plasma CysC measurements: preoperatively, 2 hours post-CPB, and on postoperative days 1 and 2.
- AKI definition: >=50% or >=0.3 mg/dl increase in serum creatinine from baseline up to 3 days post-CPB.
- Statistical analysis: Mixed linear models, receiver operating characteristic (ROC) curves, and logistic regression.
Main Results:
- AKI developed in 31.3% of patients (47/150).
- Plasma CysC levels were significantly higher at all time points in patients who developed AKI (P < 0.0001).
- The discriminatory capacity of plasma CysC for early AKI detection was modest.
Conclusions:
- Serial plasma CysC measurements are highly correlated with AKI development post-CPB.
- Plasma CysC's utility as an early diagnostic marker for AKI following CPB is limited.
- Further research may explore combined biomarkers for improved AKI prediction.
Background And Objectives:
Little is known about the performance of plasma cystatin C (CysC) in patients undergoing cardiopulmonary bypass (CPB) and its utility in the early diagnosis of acute kidney injury (AKI). In this post hoc analysis, the goal was to determine whether plasma cystatin C, measured 2 hours after the conclusion of CPB, is a reliable marker of AKI.
Design, Setting, Participants, & Measurements:
Plasma CysC was measured in 150 patients undergoing CPB at the following times: preoperatively, 2 hours after the conclusion of CPB, postoperative day 1, and postoperative day 2. Plasma CysC levels were related to the development of AKI as defined by an increase in serum creatinine of >or=50% or >or=0.3 mg/dl from baseline up to 3 days postoperative. Mixed linear models were used to evaluate the relationship of serial plasma CysC values with AKI. The discriminatory capacity of plasma CysC was estimated using receiver operating characteristic curves. Logistic regression was utilized to assess the adjusted relationship between plasma CysC and subsequent AKI.
Results:
AKI developed in 47 (31.3%) patients. Plasma CysC was higher at all times among patients who developed AKI compared with those who did not (P < 0.0001). The discriminatory capacity of plasma CysC measured preoperatively and 2 hours after the conclusion of CPB was modest.
Conclusions:
Serial measures of plasma CysC are highly correlated with the development of AKI. However, the discriminatory capacity of plasma CysC as an early marker of AKI remains limited.
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