Kyhse-Andersen J, Schmidt C, Nordin G, Andersson B, Nilsson-Ehle P, Lindström V, Grubb A
Dako A/S, Glostrup, Denmark.
Clin Chem. 1994 Oct;40(10):1921-6.
We describe a fully automated particle-enhanced turbidimetric assay for cystatin C in undiluted serum and EDTA-plasma. The throughput is 90 samples per hour and urgent samples can be analyzed in 7 min. The assay range (0.4-14.1 mg/L) covers the concentration range in health and disease. The within- and between-run imprecision is 0.9% and 2.2%, respectively. Analytical recovery of additions of recombinant cystatin C averaged 98%. Rheumatoid factors (< or = 323,000 IU/L), bilirubin (< or = 150 mumol/L), hemoglobin (< or = 1.2 g/L), and triglycerides (< or = 8.5 mmol/L) do not interfere in the assay. In view of the superior (by ROC analysis) diagnostic accuracy of serum concentrations of cystatin C for reduced glomerular filtration rate (GFR) in comparison with creatinine, cystatin C seems an attractive alternative to creatinine for estimation of GFR.
我们描述了一种用于检测未稀释血清和乙二胺四乙酸血浆中胱抑素C的全自动颗粒增强比浊法。该方法的通量为每小时90个样本,紧急样本可在7分钟内完成分析。检测范围(0.4 - 14.1 mg/L)涵盖了健康和疾病状态下的浓度范围。批内和批间不精密度分别为0.9%和2.2%。重组胱抑素C添加物的分析回收率平均为98%。类风湿因子(≤323,000 IU/L)、胆红素(≤150 μmol/L)、血红蛋白(≤1.2 g/L)和甘油三酯(≤8.5 mmol/L)在该检测中无干扰。鉴于与肌酐相比,血清胱抑素C浓度对肾小球滤过率(GFR)降低具有更高的(通过ROC分析)诊断准确性,胱抑素C似乎是用于估计GFR的肌酐的一个有吸引力的替代物。