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Clinical Chemistry 53: 480-488, 2007. First published January 26, 2007; 10.1373/clinchem.2006.076042
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(Clinical Chemistry. 2007;53:480-488.)
© 2007 American Association for Clinical Chemistry, Inc.


Endocrinology and Metabolism

Cystatin C and Estimates of Renal Function: Searching for a Better Measure of Kidney Function in Diabetic Patients

Laura Pucci1,a, Stefano Triscornia1, Daniela Lucchesi1, Carmen Fotino1, Giovanni Pellegrini2, Ennia Pardini2, Roberto Miccoli1, Stefano Del Prato1 and Giuseppe Penno1

1 Dipartimento di Endocrinologia e Metabolismo and 2 Laboratorio di Analisi Chimiche e Microbiologiche, Azienda Ospedaliero Universitaria di Pisa, Pisa, Italy.

aAddress correspondence to this author at: Dipartimento di Endocrinologia e Metabolismo, U.O. di Malattie Metaboliche e Diabetologia, Università di Pisa, 56124 Pisa, Italy. Fax 39-050-541521; e-mail plaura{at}immr.med.unipi.it.

Background: Early identification of impairment in renal function is crucial in diabetic patients. Serum cystatin C may be the most sensitive indicator of glomerular filtration rate (GFR) in the clinical setting.

Methods: We compared cystatin C with creatinine, the Cockcroft-Gault (C-G) formula, and the Modification of Diet in Renal Disease (MDRD) study equation for the assessment of early decreased renal function in 288 diabetic patients (125 type 1, 163 type 2) with renal impairment [GFR: 4–222 mL · min–1 · (1.73 m2)–1]. Relationships of cystatin C, creatinine, and iohexol clearance were linearized by plotting their reciprocals in a simple regression model. Diagnostic efficiency was calculated from ROC curves.

Results: In this study population, cystatin C (P = 0.0013) was better correlated with GFR (r = 0.857) than were creatinine (r = 0.772), C-G (r = 0.750), and MDRD (r = 0.806), a result replicated in patients with normal renal function (P = 0.023, type 1; P = 0.011, type 2), but not in those with decreased GFR. Mean cystatin C concentrations showed step-by-step statistically significant increases as GFR decreased, allowing very early detection of reduction in renal function. At 90 mL · min–1 · (1.73 m2)–1 and 75 mL · min–1 · (1.73 m2)–1 cut-points, diagnostic efficiencies of cystatin C (89% and 92%) were better than those of the other variables (79%–82% and 85%–86%, respectively; P = 0.01).

Conclusions: All data supported the value of serum cystatin C compared with conventional estimates based on serum creatinine measurement for detecting very early reduction of renal function. Use of cystatin C to measure renal function will optimize early detection, prevention, and treatment strategies for diabetic nephropathy.




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