Literature DB >> 19506046

The inaccuracy of cystatin C and creatinine-based equations in predicting GFR in orthotopic liver transplant recipients.

Neil Boudville1, Muna Salama, Gary P Jeffrey, Paolo Ferrari.   

Abstract

BACKGROUND: As survival with an orthotopic liver transplant (OLT) improves, the incidence of chronic kidney disease in OLT recipients increases. Measurement of kidney function using creatinine-based estimates is often inaccurate, while cystatin C may overcome the biases that effect creatinine. The aim of this study was to assess the accuracy of creatinine- and cystatin C-based equations to estimate kidney function in long-term OLT recipients.
METHODS: This was a cross-sectional study performed on OLT recipients within a single liver transplant centre where creatinine (n = 41) and cystatin C (n = 30) were measured and glomerular filtration rate (GFR) estimated using the Modification of Diet and Renal Disease (MDRD), Cockcroft-Gault (CG), Hoek, Larsson, Filler and Le Bricon equations. Comparison was made with the nuclear GFR (nGFR) (n = 41) measured through 51-Cr EDTA clearance.
RESULTS: The mean age of recipients was 56 +/- 13 years, and they were 6.5 +/- 4.7 years post-OLT. Fifty-six percent of recipients had a nGFR < or =60 mL/min/1.73 m(2). nGFR correlated significantly with all predictive equations (P < 0.001). The MDRD, CG and Le Bricon equations had the smallest degree of bias (-7.6, -7.3 and 3.4 mL/min/1.73 m(2), respectively), with 22%, 22% and 27% of estimates, respectively, being within 10% of nGFR measurements. In OLT recipients with nGFR < or =60 mL/min/1.73 m(2), the degree of bias of both the creatinine-base MDRD and cystatin-based Hoek equations was within 2 mL/min/1.73 m(2) difference between the measured and estimated GFR, but 41% and 36% of estimates were within 10% of the nGFR measurement.
CONCLUSIONS: Therefore, the degree of inaccuracy in cystatin C- and creatinine-based predictive equations brings into question their clinical utility in OLT recipients. We have no evidence that cystatin C is superior to creatinine in this population.

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Year:  2009        PMID: 19506046     DOI: 10.1093/ndt/gfp255

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  5 in total

1.  Performance of the Cockcroft-Gault, MDRD, and new CKD-EPI formulas in relation to GFR, age, and body size.

Authors:  Wieneke Marleen Michels; Diana Carina Grootendorst; Marion Verduijn; Elise Grace Elliott; Friedo Wilhelm Dekker; Raymond Theodorus Krediet
Journal:  Clin J Am Soc Nephrol       Date:  2010-03-18       Impact factor: 8.237

2.  Performance of cystatin C-based equations in a pediatric cohort at high risk of kidney injury.

Authors:  Edward J Nehus; Benjamin L Laskin; Thelma I Kathman; John J Bissler
Journal:  Pediatr Nephrol       Date:  2012-11-10       Impact factor: 3.714

3.  Clinical and plasma proteomic markers correlating with chronic kidney disease after liver transplantation.

Authors:  J Levitsky; D R Salomon; M Abecassis; P Langfelder; S Horvath; J Friedewald; E Wang; S M Kurian; T Mondala; S Gil; R McDade; K Ballard; L Gallon
Journal:  Am J Transplant       Date:  2011-07-27       Impact factor: 8.086

Review 4.  Hepatorenal syndrome: the 8th International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group.

Authors:  Mitra K Nadim; John A Kellum; Andrew Davenport; Florence Wong; Connie Davis; Neesh Pannu; Ashita Tolwani; Rinaldo Bellomo; Yuri S Genyk
Journal:  Crit Care       Date:  2012-02-09       Impact factor: 9.097

5.  Urine IL-18, NGAL, IL-8 and serum IL-8 are biomarkers of acute kidney injury following liver transplantation.

Authors:  Jeffrey C Sirota; Angela Walcher; Sarah Faubel; Alkesh Jani; Kim McFann; Prasad Devarajan; Connie L Davis; Charles L Edelstein
Journal:  BMC Nephrol       Date:  2013-01-17       Impact factor: 2.388

  5 in total

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