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国际临床化学联合会载脂蛋白A-I和B测定标准化项目。III. 使用国际参考物质时载脂蛋白A-I值的可比性。

International Federation of Clinical Chemistry standardization project for measurements of apolipoproteins A-I and B. III. Comparability of apolipoprotein A-I values by use of international reference material.

作者信息

Marcovina S M, Albers J J, Henderson L O, Hannon W H

机构信息

Department of Medicine, University of Washington, Seattle 98103.

出版信息

Clin Chem. 1993 May;39(5):773-81.

PMID:8485867
Abstract

In the third phase of the International Federation of Clinical Chemistry (IFCC) study for the standardization of apolipoprotein (apo) measurements, the preparation SP1-01, selected as the candidate international reference material for apo A-I, was investigated for its ability to transfer an accuracy-based value to the immunoassay calibrators and to produce comparability of the values for patients' samples. An apo A-I value of 1.50 g/L (SD 0.08 g/L) was assigned to SP1-01 by a highly standardized RIA calibrated with purified apo A-I for which the mass value had been determined by amino acid analysis. According to a common detailed protocol, the participants transferred the mass value from SP1-01 to the calibrator of each method. To confirm that uniformity of calibration ensures comparability of the values over a wide range of apo A-I values, each laboratory analyzed 50 fresh-frozen samples from individual donors, using an approach similar to that adopted by the Cholesterol Reference Laboratory Network. The consensus mean value for each sample was in excellent agreement with the value assigned by the Northwest Lipid Research Laboratories, with the average absolute bias between assigned and consensus value being 0.01 g/L. The among-laboratory CV on each of the 50 samples ranged from 2.1% to 5.6% (mean 3.6%), demonstrating that comparable apo A-I results can be obtained by a variety of immunochemical methods through the use of certified reference material. Based on the results obtained in these studies, SP1-01 has been approved as Apolipoprotein A-I International Reference Material by the World Health Organization.

摘要

在国际临床化学联合会(IFCC)载脂蛋白(apo)测量标准化研究的第三阶段,对被选为apo A-I候选国际参考物质的制剂SP1-01进行了研究,考察其将基于准确度的值传递至免疫测定校准品以及使患者样本值具有可比性的能力。通过用经氨基酸分析确定了质量值的纯化apo A-I校准的高度标准化放射免疫分析(RIA),给SP1-01赋予了1.50 g/L(标准差0.08 g/L)的apo A-I值。按照一个通用的详细方案,参与者将质量值从SP1-01传递至每种方法的校准品。为确证校准的一致性可确保在很宽的apo A-I值范围内各值具有可比性,每个实验室使用与胆固醇参考实验室网络所采用方法类似的方法分析了来自个体供者的50份新鲜冷冻样本。每个样本的一致均值与西北脂质研究实验室指定的值高度吻合,指定值与一致值之间的平均绝对偏差为0.01 g/L。50个样本中每个样本的实验室间变异系数(CV)在2.1%至5.6%之间(均值3.6%),表明通过使用经认证的参考物质,多种免疫化学方法可获得可比的apo A-I结果。基于这些研究获得的结果,SP1-01已被世界卫生组织批准为载脂蛋白A-I国际参考物质。

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