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Serum Cystatin C as an Indicator of Renal Function and Mortality in Liver Transplant Recipients
Alina M Allen1, W Ray Kim, Joseph J Larson
11 Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN. 2 Division of Gastroenterology and Hepatology, Stanford University, Stanford, CA. 3 Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN. 4 Division of Nephrology, Mayo Clinic, Rochester, MN.
Background/Aims:
Chronic kidney disease (CKD) is an important comorbidity after liver transplantation (LT); however, reliable tools with which to evaluate these patients are limited. In this work, we examine the extent to which the addition of serum cystatin C improves glomerular filtration rate (GFR) estimation and mortality prediction, in comparison to various GFR-estimating equations.
Methods:
The GFR was measured in LT recipients by iothalamate clearance. Concurrent serum cystatin C was assayed in banked serum samples. Performance of GFR-estimating equations with and without cystatin C, including the modification of diet in renal disease and CKD-epidemiology collaboration formulas was assessed. The proportional hazards regression analysis was performed to determine the association between serum cystatin C and mortality.
Results:
A total of 586 iothalamate results were obtained in 401 patients after a mean of 4 years after LT. When compared to measured GFR, the formula with both creatinine and cystatin C, namely, CKD-epidemiology cr-cys, outperformed those with either marker alone. Performance of creatinine-based models was similar to one another. Serum cystatin C, by itself or as a part of an estimated GFR, was a significant predictor of mortality.
Conclusions:
Serum cystatin C has an important role in enhancing accuracy of GFR estimation and predicting mortality in LT recipients.
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