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测量生长激素的同位素和非同位素检测方法比较:激发试验中临界值的重新评估

Isotopic and nonisotopic assays for measuring somatotropin compared: re-evaluation of cutoff value in provocative tests.

作者信息

Banfi G, Marinelli M, Casari E, Murone M, Bonini P

机构信息

Laboratorio Analisi, Istituto Scientifico H.S. Raffaele, Milano, Italy.

出版信息

Clin Chem. 1991 Feb;37(2):273-6.

PMID:1993338
Abstract

Measurement of human growth hormone (hGH; somatotropin) concentrations in serum after provocative tests is crucial for diagnosing deficiencies in production of this hormone. Serum hGH can be measured by various immunoassays, isotopic and nonisotopic, with monoclonal or polyclonal antibodies: a cutoff value of 10 micrograms/L after provocative testing is usually used to distinguish normal from hGH-deficient children. Previous studies demonstrated discrepancies in hGH measurement by different radioisotopic immunoassays. Here we evaluated the responses of six different commercial assays, radioisotopic and nonisotopic, with monoclonal or polyclonal antibodies in a series of 16 provocative tests (stimulation with clonidine) in short children. A wide range of discrepant values was obtained with the different kits. A cutoff of 10 micrograms/L produced discordance of diagnosis among assays for two children, whereas complete agreement was reached for a cutoff value of 7 micrograms/L. Parallelism tests performed with hGH international standard, pure recombinant hGH, and a serum with high hGH content suggest that heterogeneity of the antibodies used by the manufacturers, even among monoclonal antibodies, is the main source of discordant results. Cutoff values and reference values must be established separately for each method proposed for routine use.

摘要

在激发试验后测量血清中人类生长激素(hGH;促生长激素)浓度对于诊断该激素分泌不足至关重要。血清hGH可通过各种免疫测定法进行测量,包括同位素和非同位素方法,使用单克隆或多克隆抗体:激发试验后通常以10微克/升的临界值来区分正常儿童和hGH缺乏儿童。先前的研究表明,不同的放射性同位素免疫测定法在hGH测量方面存在差异。在此,我们评估了六种不同的商业检测方法,包括放射性同位素和非同位素方法,使用单克隆或多克隆抗体,对一系列16名身材矮小儿童进行了可乐定刺激激发试验。不同试剂盒获得了广泛的差异值。以10微克/升为临界值时,两种检测方法之间对两名儿童的诊断存在不一致,而以7微克/升为临界值时则达成了完全一致。使用hGH国际标准品、纯重组hGH和hGH含量高的血清进行的平行试验表明,制造商使用的抗体存在异质性,即使在单克隆抗体中也是如此,这是结果不一致的主要原因。对于每种建议用于常规检测的方法,必须分别确定临界值和参考值。

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