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Comparison between Cystatin C- and Creatinine-Estimated Glomerular Filtration Rate in Cardiology Patients
Axel Åkerblom1, Johanna Helmersson-Karlqvist2, Mats Flodin2
1Department of Medical Sciences, University Hospital, Uppsala University, Uppsala, Sweden ; Uppsala Clinical Research Center, Uppsala, Sweden ; Duke Clinical Research Institute, Durham, N.C., USA.
Insights
Creatinine-based estimated glomerular filtration rate (eGFR) is higher than cystatin C eGFR in cardiology patients, potentially leading to misinterpretation and incorrect medication. Awareness of the eGFR method is crucial.
Area of Science:
- Nephrology
- Cardiology
- Clinical Chemistry
Background:
- Glomerular filtration rate (GFR) estimation is vital for diagnosing kidney disease, predicting patient risk, and guiding drug dosages.
- Both cystatin C and creatinine are commonly used biomarkers for GFR estimation.
- Discrepancies in GFR estimation can impact clinical decision-making, particularly in cardiac patients.
Purpose of the Study:
- To investigate the differences between estimated GFR (eGFR) calculated using cystatin C and creatinine in a diverse cardiology patient population.
- To assess the clinical implications of these differences on patient categorization and risk stratification.
Main Methods:
- An observational, cross-sectional study was conducted involving 5,678 cardiology patients across various care settings (outpatient, ward, CCU, advanced CCU).
- Estimated GFR was calculated using both cystatin C and creatinine (CKD-EPI) from the same laboratory requests.
- Data were analyzed to compare the eGFR values obtained from the two methods.
Main Results:
- Median creatinine eGFR was consistently higher than median cystatin C eGFR, with a difference of approximately 10 ml/min/1.73 m(2) across all care levels.
- For patients with a cystatin C eGFR below 60 ml/min/1.73 m(2), creatinine eGFR often placed them in a less advanced kidney disease category.
- The observed differences were independent of the level of care provided to the cardiology patients.
Conclusions:
- Significant differences exist between creatinine and cystatin C eGFR in cardiology patients.
- Clinicians must be aware of the specific biomarker used for eGFR reporting to prevent misinterpretation of results.
- Understanding these differences is critical to avoid potential under- or over-medication and requires further research to establish the optimal GFR estimation method for cardiology units.
Objective:
Estimation of the glomerular filtration rate (GFR) is essential for identification, evaluation and risk prediction in patients with kidney disease. Estimated GFR (eGFR) is also needed for the correct dosing of drugs eliminated by the kidneys and to identify high-risk individuals in whom coronary angiography or other procedures may lead to kidney failure. Both cystatin C and creatinine are used for the determination of GFR, and we aimed to investigate if eGFR by the two methods differ in cardiology patients.
Methods:
We compared cystatin C and creatinine (CKD-EPI) eGFR calculated from the same request from a cardiology outpatient unit (n = 2,716), a cardiology ward (n = 980), a coronary care unit (n = 1,464), and an advanced coronary care unit (n = 518) in an observational, cross-sectional study.
Results:
The median creatinine eGFR results are approximately 10 ml/min/1.73 m(2) higher than the median cystatin C eGFR that is up to 90 ml/min/1.73 m(2), irrespective of the level of care. Creatinine eGFR resulted in a less advanced eGFR category in the majority of patients with a cystatin C eGFR <60 ml/min/1.73 m(2).
Conclusions:
Our study demonstrates a difference between creatinine and cystatin C eGFR in cardiology patients. It is important to be aware of which marker is used for the reported eGFR to minimize erroneous interpretations of the test results, as this could lead to under- or overmedication. Further studies are needed to determine the best method of estimating the GFR in cardiology units.
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