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Clinical Chemistry 43: 1016-1022, 1997;
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(Clinical Chemistry. 1997;43:1016-1022.)
© 1997 American Association for Clinical Chemistry, Inc.


Articles

Initial evaluation of cystatin C measurement by particle-enhanced immunonephelometry on the Behring nephelometer systems (BNA, BN II)

Hazel Finney1, David J. Newman1,a, Walter Gruber2, Peter Merle2 and Christopher P. Price1

1 Department of Clinical Biochemistry, St. Bartholomew's and The Royal London School of Medicine and Dentistry, Turner St., London E1 2AD, UK.

2 Behringwerke AG, Postfach 1140, D-35001 Marburg, Germany.
a Author for correspondence. Fax +(44) 171 377 1544; e-mail d.j.newman{at}mds.qmw.ac.uk

Serum cystatin C has been suggested as a new marker of glomerular filtration rate (GFR). We describe a fully automated and rapid particle-enhanced nephelometric immunoassay (PENIA) for measuring serum cystatin C on the Behring nephelometer systems (BNA, BN II). Each sample is analyzed in 6 min with as many as 75 samples per batch. The assay covers the range 0.23–7.25 mg/L, up to seven times the upper limit of normal. The intra- and interassay imprecision are <3.3% and <4.5%, respectively. There is absolute linearity across the assay range (r2 = 0.997), with analytical recovery by cystatin C addition between 95% and 109% (mean 102%). Hemoglobin (<=8.0 g/L), bilirubin (<=488 µL), triglycerides (<=23 mmol/L), rheumatoid factor (<=2000 kIU/L), and myeloma paraprotein (<=41 g/L) do not interfere with the assay. This assay agreed well with an in-house particle-enhanced turbidimetric immunoassay (PETIA) (mean difference = 1.73 ± 2.10) and a commercial PETIA (mean difference = 1.13 ± 0.86). This is a new assay by which cystatin C may be effectively used as a marker of GFR estimation.


Key Words: indexing terms: kidney function • immunoassay • glomerular filtration rate




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S. K. Swan
The Search Continues--An Ideal Marker of GFR
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