Literature DB >> 17259236

Cystatin C and estimates of renal function: searching for a better measure of kidney function in diabetic patients.

Laura Pucci1, Stefano Triscornia, Daniela Lucchesi, Carmen Fotino, Giovanni Pellegrini, Ennia Pardini, Roberto Miccoli, Stefano Del Prato, Giuseppe Penno.   

Abstract

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 x min(-1) x (1.73 m(2))(-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 x min(-1) x (1.73 m(2))(-1) and 75 mL x min(-1) x (1.73 m(2))(-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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Year:  2007        PMID: 17259236     DOI: 10.1373/clinchem.2006.076042

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  49 in total

1.  Early renal function decline in type 2 diabetes.

Authors:  Meda E Pavkov; William C Knowler; Kevin V Lemley; Clinton C Mason; Bryan D Myers; Robert G Nelson
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2.  Insufficient performance of serum cystatin C as a biomarker for acute kidney injury of postrenal etiology.

Authors:  Julia Hasslacher; Georg F Lehner; Michael Joannidis
Journal:  Intensive Care Med       Date:  2011-10-01       Impact factor: 17.440

3.  Reference values for serum creatinine in children younger than 1 year of age.

Authors:  Dirk P Boer; Yolanda B de Rijke; Wim C Hop; Karlien Cransberg; Eiske M Dorresteijn
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Review 4.  The applicability of eGFR equations to different populations.

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5.  Cystatin C identifies patients with stable chronic heart failure at increased risk for adverse cardiovascular events.

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6.  Normoalbuminuric chronic kidney disease in type 1 diabetes: is it real and is it serious? Reply to Rigalleau V, Blanco L, Alexandre L et al [letter].

Authors:  Giuseppe Penno; Eleonora Russo; Monia Garofolo; Giuseppe Daniele; Daniela Lucchesi; Laura Giusti; Veronica Sancho Bornez; Cristina Bianchi; Angela Dardano; Roberto Miccoli; Stefano Del Prato
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7.  Elevated serum cystatin C in severe OSA younger men without complications.

Authors:  Xiao-Bin Zhang; Qi-Chang Lin; Chao-Sheng Deng; Gong-Ping Chen; Zhi-Ming Cai; Hua Chen
Journal:  Sleep Breath       Date:  2012-03-16       Impact factor: 2.816

8.  Serum cystatin C as a marker to identify patients with moderately impaired renal function.

Authors:  H Peiris; L G Chandrasena; R D Lanerolle
Journal:  Indian J Clin Biochem       Date:  2008-06-11

Review 9.  Application of "omics" to prion biomarker discovery.

Authors:  Rhiannon L C H Huzarewich; Christine G Siemens; Stephanie A Booth
Journal:  J Biomed Biotechnol       Date:  2010-03-04

10.  Cystatin C is downregulated in prostate cancer and modulates invasion of prostate cancer cells via MAPK/Erk and androgen receptor pathways.

Authors:  Barbara Wegiel; Thomas Jiborn; Magnus Abrahamson; Leszek Helczynski; Leo Otterbein; Jenny Liao Persson; Anders Bjartell
Journal:  PLoS One       Date:  2009-11-23       Impact factor: 3.240

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