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欧洲临床实验室中总睾酮、性激素结合球蛋白和游离睾酮测量与报告情况的调查。

A survey on measurement and reporting of total testosterone, sex hormone-binding globulin and free testosterone in clinical laboratories in Europe.

作者信息

Narinx Nick, Nyamaah Jennifer Afrakoma, David Karel, Sommers Vera, Walravens Joeri, Fiers Tom, Lapauw Bruno, Decallonne Brigitte, Claessens Frank, Van Uytfanghe Katleen, Billen Jaak, Vermeersch Pieter, Vanderschueren Dirk, Antonio Leen

机构信息

Laboratory of Clinical and Experimental Endocrinology, Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.

Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.

出版信息

Clin Chem Lab Med. 2025 Mar 12;63(8):1561-1572. doi: 10.1515/cclm-2024-1237. Print 2025 Jul 28.

Abstract

OBJECTIVES

To compare clinical laboratory workflows for the assessment of androgens in men, focusing on total testosterone (T), sex hormone-binding globulin (SHBG) and free T, in clinical laboratories throughout Europe.

METHODS

An internet-based survey that included questions related to pre-analytical, analytical and post-analytical phases of androgen measurements was distributed between December 2022 and December 2023 by clinical laboratory/chemistry and endocrine societies. A total of 124 unique records from clinical laboratories in 27 European countries were analyzed.

RESULTS

Pre-analytical requirements for total T are subject to improvement as less than half of clinical laboratories recommended adequate morning sampling time and/or sampling in a fasting state. Total T was predominantly quantified using enzyme-linked immunoassay (IA) on automated platforms, with only one in four centers using mass spectrometry (MS), while SHBG was exclusively measured by IA. Additionally, free T was used by a majority of clinical laboratories, mainly reported as approximation by calculation of free T (cFT) using the Vermeulen formula. Generally, age-stratification was the preferred means of reporting reference ranges for total T, SHBG and cFT. However, considerate variability was observed in reported lower and upper limits, leading to the necessity of interpreting test results against assay-specific reference ranges, thereby hindering comparability of results between clinical laboratories.

CONCLUSIONS

Our survey highlights significant inter-laboratory variability for the assessment of androgen status in men, implying non-commutability of clinical test results between different centers. In addition, we observed poor adherence to pre-analytical recommendations. These findings advocate for continued harmonization efforts of measurement procedures for SHBG and total/free T.

摘要

目的

比较欧洲各临床实验室评估男性雄激素(重点关注总睾酮(T)、性激素结合球蛋白(SHBG)和游离T)的临床实验室工作流程。

方法

临床实验室/化学和内分泌学会在2022年12月至2023年12月期间开展了一项基于互联网的调查,其中包括与雄激素测量的分析前、分析和分析后阶段相关的问题。共分析了来自27个欧洲国家临床实验室的124条独特记录。

结果

总T的分析前要求有待改进,因为不到一半的临床实验室建议采用适当的早晨采样时间和/或空腹状态下采样。总T主要在自动化平台上使用酶联免疫分析(IA)进行定量,只有四分之一的中心使用质谱(MS),而SHBG仅通过IA测量。此外,大多数临床实验室使用游离T,主要报告为使用Vermeulen公式计算游离T(cFT)的近似值。一般来说,年龄分层是报告总T、SHBG和cFT参考范围的首选方法。然而,报告的下限和上限存在相当大的差异,这就需要根据特定检测方法的参考范围来解释检测结果,从而阻碍了临床实验室之间结果的可比性。

结论

我们的调查突出了男性雄激素状态评估中实验室间的显著差异,这意味着不同中心的临床检测结果不可互换。此外,我们观察到对分析前建议的遵守情况较差。这些发现主张继续努力统一SHBG和总/游离T的测量程序。

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