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酒精生物标志物缺糖转铁蛋白(CDT)的标准化与应用再版

Reprint of Standardisation and use of the alcohol biomarker carbohydrate-deficient transferrin (CDT).

作者信息

Helander Anders, Wielders Jos, Anton Raymond, Arndt Torsten, Bianchi Vincenza, Deenmamode Jean, Jeppsson Jan-Olof, Whitfield John B, Weykamp Cas, Schellenberg François

机构信息

Karolinska Institutet and Karolinska University Laboratory, Stockholm, Sweden.

Meander Medisch Centrum, Amersfoort, The Netherlands.

出版信息

Clin Chim Acta. 2017 Apr;467:15-20. doi: 10.1016/j.cca.2017.03.018. Epub 2017 Mar 18.

Abstract

Carbohydrate-deficient transferrin (CDT) is a glycoform profile of serum transferrin that increases in response to sustained high alcohol intake and over the last decades has become an important alcohol biomarker with clinical and forensic applications. However, the wide range of CDT measurement procedures has resulted in lack of uniform results and reference limits, and hampered comparison of results. In 2005, the IFCC therefore founded a special working group (WG) aiming for standardisation of CDT measurement. This review summarises the history of CDT and the actions taken by the WG-CDT. Initial steps included the definition of the measurand (serum disialotransferrin to total transferrin fraction expressed in %), and the determination of a well-defined anion-exchange HPLC procedure as the candidate reference measurement procedure (cRMP). Subsequent achievements were the establishment of a network of reference laboratories to perform the cRMP, setting a reference interval, and development of a reference material based on human serum for which the laboratory network assign values. Using a set of reference materials for calibration allowed for achieving equivalence of results of all present CDT measurement procedures. The final steps of the WG-CDT have been a full validation of the cRMP to make it an IFCC approved RMP, and providing guidance for international standardisation of all CDT measurement procedures.

摘要

缺糖转铁蛋白(CDT)是血清转铁蛋白的一种糖型谱,其水平会因持续大量饮酒而升高,在过去几十年中已成为一种具有临床和法医应用价值的重要酒精生物标志物。然而,CDT测量方法种类繁多,导致结果缺乏一致性且参考限值不统一,阻碍了结果的比较。因此,国际临床化学与检验医学联合会(IFCC)于2005年成立了一个特别工作组(WG),旨在实现CDT测量的标准化。本综述总结了CDT的历史以及CDT工作组所采取的行动。最初的步骤包括被测量物的定义(血清双唾液酸转铁蛋白与总转铁蛋白的比例,以%表示),以及确定一种明确的阴离子交换高效液相色谱法作为候选参考测量程序(cRMP)。随后取得的成果包括建立一个参考实验室网络来执行cRMP、设定参考区间,以及开发一种基于人血清的参考物质,由该实验室网络为其赋值。使用一组参考物质进行校准可使所有现有CDT测量程序的结果实现等效。CDT工作组的最后步骤是对cRMP进行全面验证,使其成为IFCC认可的RMP,并为所有CDT测量程序的国际标准化提供指导。

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