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描述和验证一种用于人血清中游离甲状腺素的平衡透析 LC-MS/MS 候选参考测量程序。

Description and validation of an equilibrium dialysis ID-LC-MS/MS candidate reference measurement procedure for free thyroxine in human serum.

机构信息

Department of Clinical Chemistry, Endocrine Laboratory, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Department of Clinical Chemistry, Endocrine Laboratory, Amsterdam UMC Location University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Clin Chem Lab Med. 2023 Mar 31;61(9):1605-1611. doi: 10.1515/cclm-2022-1134. Print 2023 Aug 28.

Abstract

OBJECTIVES

Free thyroxine (FT4) in serum is routinely measured in clinical practice to diagnose and monitor thyroid disease. Due to its concentration in picomolar range and the delicate equilibrium of free and protein-bound T4, accurate measurement is challenging. As a consequence, large inter-method differences in FT4 results exists. Optimal method design and standardization of the FT4 measurement is therefore necessary. The IFCC Working Group for Standardization of Thyroid Function Tests proposed a reference system with a conventional reference measurement procedure (cRMP) for FT4 in serum. In this study, we describe our FT4 candidate cRMP and its validation in clinical samples.

METHODS

This candidate cRMP is based on equilibrium dialysis (ED) combined with determination of T4 with an isotope-dilution liquid chromatography tandem mass-spectrometry (ID-LC-MS/MS) procedure and was developed according to the endorsed conventions. Its accuracy, reliability, and comparability was investigated using human sera.

RESULTS

It was shown that the candidate cRMP adhered to the conventions and its accuracy, precision, and robustness were adequate in serum of healthy volunteers.

CONCLUSIONS

Our candidate cRMP measures FT4 accurately and performs well in serum matrix.

摘要

目的

在临床实践中,通常会测量血清中的游离甲状腺素 (FT4),以诊断和监测甲状腺疾病。由于其浓度处于皮摩尔范围内,并且游离和结合 T4 之间的平衡非常微妙,因此准确测量具有挑战性。因此,FT4 结果存在很大的方法间差异。因此,有必要对 FT4 测量进行最佳方法设计和标准化。国际临床化学联合会 (IFCC) 甲状腺功能测试标准化工作组提出了一个参考系统,其中包括血清中常规参考测量程序 (cRMP) 的 FT4。在这项研究中,我们描述了我们的 FT4 候选 cRMP 及其在临床样本中的验证。

方法

该候选 cRMP 基于平衡透析 (ED),结合使用同位素稀释液相色谱串联质谱 (ID-LC-MS/MS) 程序测定 T4,并根据认可的常规进行了开发。使用人血清研究了其准确性、可靠性和可比性。

结果

结果表明,候选 cRMP 符合常规要求,其在健康志愿者血清中的准确性、精密度和稳健性均足够。

结论

我们的候选 cRMP 可以准确测量 FT4,并且在血清基质中表现良好。

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