Renal dysfunction of variable severity is being increasingly recognized as a major complication of calcineurin inhibitors (CI), in some patients even necessitating renal transplantation. Close and effective monitoring of the renal function is indicated. Current methods for this monitoring are calculation of the glomerular filtration rate (GFR) based on creatinine or exogenous substances like 51 Cr-EDTA. The first method is unreliable in children and the second is expensive and cumbersome. Cystatin C has been shown to be an accurate marker of glomerular filtration but has not been evaluated in a large cohort of pediatric patients before and after liver transplantation (LT). We evaluated the accuracy of cystatin C in 62 children ( C alcineurin inhibitors (CI), cyclosporin, and tacrolimus have significantly contributed toward improved long-term survival of children after solid organ transplantation. 1 The current 5-year survival of children after liver transplantation (LT) is above 85% in most centers. Nephrotoxicity of variable severity is one of the most serious side effects of CI treatment, at times necessitating renal transplantation. 2 The incidence of nephrotoxicity in non-renal allograft patients is between 20% and 70%. 3 Although newer immunosuppressive drugs, like mycophenolate mofetil (MMF) and rapamicin, are not nephrotoxic, their use is still limited to rescue therapy for renal dysfunction or resistant cellular rejection. A large cohort of children worldwide is maintained on CI as anti-rejection drugs. In order to avoid irreversible renal damage, close and effective monitoring of their renal function is necessary. The gold standard for measuring glomerular function is inulin clearance or 51 Cr-EDTA estimation. Both methods are cumbersome and expensive, and 51 Cr-EDTA estimation requires administration of a radioactive substance. Serum creatinine is the endogenous substance most commonly used for estimation of glomerular filtration rate (GFR), but it is influenced by muscle mass, age, and gender, thus affecting its value in children. 4 A simple test to evaluate renal function in pediatric patients is highly desirable. Cystatin C, a low molecular weight protein, has recently been proposed as a reliable marker of renal function both in adults and children. 5 -15 After clearance from the plasma via glomerular filtration, cystatin C is completely reabsorbed and catabolized in the renal tubules. 7 Adult ranges are reached by the age of 1 year and are not influenced by gender, height, or body composition. 11 Reference ranges for both adults and children are available. 9 -14,16 Cystatin C has been assessed in adult and pediatric renal transplant recipients 9,16 -18 and in adults after liver transplantation, 19,20 but information is lacking in pediatric liver transplant recipients. The aim of this study was to evaluate cystatin C as a marker of renal function in a large cohort of pediatric patients with chronic liver disease and after liver transplantation.