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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Generation of a new cystatin C-based estimating equation for glomerular filtration rate by use of 7 assays standardized to the international calibrator
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Generation of a new cystatin C-based estimating equation for glomerular filtration rate by use of 7 assays standardized to the international calibrator

机译:通过使用国际校准品标准化的7种测定方法,生成新的基于半胱氨​​酸蛋白酶抑制剂C的肾小球滤过率估计方程

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BACKGROUND: Many different cystatin C-based equations exist for estimating glomerular filtration rate. Major reasons for this are the previous lack of an international cystatin C calibrator and the nonequivalence of results from different cystatin C assays. METHODS: Use of the recently introduced certified reference material, ERM-DA471/IFCC, and further work to achieve high agreement and equivalence of 7 commercially available cystatin C assays allowed a substantial decrease of the CV of the assays, as defined by their performance in an external quality assessment for clinical laboratory investigations. By use of 2 of these assays and a population of 4690 subjects, with large subpopulations of children and Asian and Caucasian adults, with their GFR determined by either renal or plasma inulin clearance or plasma iohexol clearance, we attempted to produce a virtually assay-independent simple cystatin C-based equation for estimation of GFR. RESULTS: We developed a simple cystatin C-based equation for estimation of GFR comprising only 2 variables, cystatin C concentration and age. No terms for race and sex are required for optimal diagnostic performance. The equation, eGFR=130 × cystatin C -1.069 × age-0.117-7, is also biologically oriented, with 1 term for the theoretical renal clearance of small molecules and 1 constant for extrarenal clearance of cystatin C. CONCLUSIONS: A virtually assay-independent simple cystatin C-based and biologically oriented equation for estimation of GFR, without terms for sex and race, was produced.
机译:背景:存在许多不同的基于胱抑素C的方程式,用于估计肾小球滤过率。造成这种情况的主要原因是以前缺乏国际化的胱抑素C校准品,以及不同的胱抑素C测定结果不相等。方法:使用最近引入的认证参考材料ERM-DA471 / IFCC,以及为实现7种市售胱抑素C测定法的较高一致性和等效性而进行的进一步工作,使测定法的CV大大降低,这由其在以下条件下的性能确定用于临床实验室调查的外部质量评估。通过使用其中2种检测方法和4690名受试者,儿童和亚洲及高加索成年人的大量亚群,通过肾或血浆菊粉清除率或血浆碘海醇清除率测定GFR,我们尝试产生一种与检测无关的方法基于半胱氨​​酸蛋白酶抑制剂C的简单方程估算GFR。结果:我们开发了一个简单的基于半胱氨​​酸蛋白酶抑制剂C的方程,用于评估GFR,该方程仅包含两个变量,即半胱氨酸蛋白酶抑制剂C浓度和年龄。最佳诊断性能不需要种族和性别的条件。方程eGFR = 130×胱抑素C -1.069×年龄-0.117-7也是生物学取向的,其中1个术语表示小分子的理论肾清除率,1个常数表示cystatin C的肾外清除率。产生了独立的简单的基于半胱氨​​酸蛋白酶抑制剂C的,基于生物学的GFR估算方程,其中没有性别和种族的术语。

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