Analytical validation based on total error measurement and cut-off interpretation of a neonatal screening TSH-immunoassay

被引:10
作者
Boemer, Francois [1 ]
Bours, Vincent [1 ]
Schoos, Roland [1 ]
Hubert, Philippe [2 ]
Rozet, Eric [2 ]
机构
[1] Univ Liege, CHU, Ctr Genet Humaine, Biochim Genet Lab, B-4000 Liege, Belgium
[2] Univ Liege, Dept Pharm, CIRM, Analyt Chem Lab, B-4000 Liege, Belgium
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 23期
关键词
Neonatal screening; Congenital hypothyroidism; Validation; Total error; Accuracy profile; THYROID-STIMULATING HORMONE; QUANTITATIVE ANALYTICAL PROCEDURES; SFSTP PROPOSAL; IODINE DEFICIENCY; HARMONIZATION; STRATEGIES; ASSAYS; HYPOTHYROIDISM; PEROXIDASE; ANTIBODY;
D O I
10.1016/j.jchromb.2008.11.004
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
To prevent the severe developmental and physical morbidities associated with congenital hypothyroidism, we developed a home-made Enzyme-Linked Immunosorbent Assay (ELISA) method to quantify Thyroid Stimulating Hormone (TSH) levels on newborn dried blood spots. In order to agree with actual clinical laboratory quality referential (ISO 15189), we desired to update our analytical validation protocol. For this purpose, an approach using accuracy profiles based on tolerance intervals for the total error measurement was for first time applied to an immunological assay. According to acceptance limits fixed at +/- 30%, the method was found accurate over a concentration range from 17.48 to 250 mIU/L. Based on 99.5 percentile of a 16,459 newborn population, cut-off was fixed at 20.1 mIU/L and validated against normal and pathologic neonatal populations. Additionally, uncertainty regions around this value were obtained applying four different approaches. Finally, we demonstrated here our in-house immunological technique fulfils criterions of a neonatal screening policy. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2412 / 2417
页数:6
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