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Articles |
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 0.237.25 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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