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Clinical Chemistry 48: 729-736, 2002;
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Right arrow Proteomics and Protein Markers
(Clinical Chemistry. 2002;48:729-736.)
© 2002 American Association for Clinical Chemistry, Inc.

ß-Trace Protein, Cystatin C, ß2-Microglobulin, and Creatinine Compared for Detecting Impaired Glomerular Filtration Rates in Children

Guido Filler1, Friedrich Priem2a, Nathalie Lepage3, Pranav Sinha2, Ilka Vollmer4, Heather Clark5, Erin Keely5, Mary Matzinger6, Ayub Akbari5, Harald Althaus7 and Klaus Jung8

Departments of
1 Pediatrics,
3 Biochemistry, and
6 Radiology, Children’s Hospital of Eastern Ontario, Ottawa, Ontario, K1H 8L1 Canada.
5 Department of Medicine, University of Ottawa, Ottawa, Ontario, K1N 6N5 Canada.
Departments of
2 Laboratory Medicine,
4 Pediatric Nephrology, and
8 Urology, University Hospital Charité, Humboldt University, D-10117 Berlin, Germany.

7 Dade Behring GmbH, Marburg, Germany.

aAddress correspondence to this author at: Institute of Laboratory Medicine and Pathobiochemistry, University Hospital Charité, Humboldt University Berlin, Schumannstrasse 20/21, D-10117 Berlin, Germany. Fax 4930-450569912; e-mail friedrich.priem{at}charite.de.

Background: Because of the limitations of serum creatinine as a marker of glomerular filtration rate (GFR) in children, we assessed the diagnostic accuracy of the novel marker ß-trace protein (BTP) in comparison with cystatin C (Cys-C), ß2-microglobulin 2-MG), and creatinine as conventional indicators of reduced GFR.

Methods: We obtained serum samples from 225 children (age range, 0.2–18 years) with various renal pathologies who were referred for nuclear medicine clearance investigations (technetium-diethylenetriamine pentaacetic acid or chromium-EDTA). We measured Cys-C, BTP (nephelometric tests; Dade Behring), ß2-MG (Tinaquant; Roche), and creatinine (enzymatic assay; Creatinine-PAP; Roche).

Results: Seventy-five children had reduced GFR (<90 mL · min-1 · 1.73 m-2). One hundred fifty children (independent of gender and age) with values >90 mL · min-1 · 1.73 m-2 comprised the control group with gaussian distributions of BTP and Cys-C concentrations. The upper reference limits (97.5 percentile) were 1.01 mg/L for BTP and 1.20 mg/L for Cys-C. The correlations of nuclear medicine clearance with the reciprocals of BTP, Cys-C, and the Schwartz GFR estimate were significantly higher (r = 0.653, 0.765, and 0.706, respectively; P <0.05) than with the reciprocal of creatinine or ß2-MG (r = 0.500 and 0.557, respectively). ROC analysis showed a significantly higher diagnostic accuracy of BTP, Cys-C, and the GFR estimate for the detection of impaired GFR than serum creatinine (P <0.05). Compared to creatinine, BTP increased the diagnostic sensitivity by ~30%, but it was not more sensitive than Cys-C or the Schwartz GFR estimate.

Conclusions: BTP is superior to serum creatinine and an alternative for Cys-C to detect mildly reduced GFR in children, but it is not better than the Schwartz GFR estimate.




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