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用于甲状旁腺激素(PTH)测量协调的液相色谱-质谱联用(LC-MS)候选参考方法:近期进展与未来考量综述

LC-MS candidate reference methods for the harmonisation of parathyroid hormone (PTH) measurement: a review of recent developments and future considerations.

作者信息

Couchman Lewis, Taylor David R, Krastins Bryan, Lopez Mary F, Moniz Cajetan F

出版信息

Clin Chem Lab Med. 2014 Sep;52(9):1251-63. doi: 10.1515/cclm-2014-0150.

DOI:10.1515/cclm-2014-0150
PMID:24762644
Abstract

The analysis of intact parathyroid hormone (PTH) (PTH1-84) is useful in the diagnosis of hyper- and hypocalcaemia, hyperparathyroidism, and in the prevention of bone mineral disorders in renal patients. The analysis is complicated by the presence of PTH fragments, which may accumulate in renal failure and cross-react in immunoassays, including the most recent third-generation immunoassays. Large variability exists between different commercially available assays. This article reviews the current literature on PTH testing, with emphasis on the use of mass spectrometry-based methods, and considers the important sources of variation which still need to be addressed prior to the development of much needed candidate reference methods for PTH analysis. Recently, mass spectrometric methods have been developed for the quantitation of PTH1-84 using surrogate tryptic peptides, but even these methods are subject to significant interferences due to the presence of newly observed modified PTH species, such as oxidised and phosphorylated PTH variants, which can accumulate in patient samples. Further work, including: 1) the use of high-resolution mass spectrometry; and 2) the analysis of PTH without prior protease digestion, is required before these approaches can be considered as reference methods against which other methods should be harmonised.

摘要

完整甲状旁腺激素(PTH)(PTH1-84)分析在高钙血症和低钙血症、甲状旁腺功能亢进的诊断以及肾疾病患者骨矿物质紊乱的预防中具有重要作用。由于PTH片段的存在,该分析变得复杂,这些片段可能在肾衰竭时蓄积,并在免疫测定(包括最新的第三代免疫测定)中发生交叉反应。不同的市售检测方法之间存在很大差异。本文回顾了当前关于PTH检测的文献,重点是基于质谱的方法,并考虑了在开发急需的PTH分析候选参考方法之前仍需解决的重要变异来源。最近,已开发出使用替代胰蛋白酶肽定量PTH1-84的质谱方法,但由于新观察到的修饰PTH物种(如氧化和磷酸化PTH变体)的存在,这些方法也受到显著干扰,这些变体可在患者样本中蓄积。在这些方法可被视为其他方法应与之协调的参考方法之前,还需要进一步开展工作,包括:1)使用高分辨率质谱;2)无需事先进行蛋白酶消化即可分析PTH。

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