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Critical evaluation of assays for vitamin D status

机译:评估维生素D状况的关键评估

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PURPOSE OF REVIEW: The objective is to highlight new aspects and methodological developments in the assessment of vitamin D status in clinical settings. RECENT FINDINGS: Recent advances in the assessment of vitamin D status mostly concern two areas: the emerging clinical and analytical interest in other circulating vitamin D metabolites [i.e. 3-epimer and 24,25-(OH)2 D] that opens a new perspective for the vitamin D metabolite profiling in health and disease and methodological improvements including the development of reference measurement procedures, the certification of Standard Reference Materials, the development and application of Standardization protocols and the change of the Vitamin D External Quality Assurance Survey (DEQAS) to an accuracy-based proficiency testing scheme. SUMMARY: Despite the improvement in the analytical imprecision between methods and laboratories over the last years, the reported prevalence of vitamin D deficiency in a given population still depends on the method used. Improvements in quality control procedures, however, will improve the standardization, accuracy and comparability of methods. At present, the analytical evaluation of other circulating vitamin D metabolites (vitamin D profiling) and their clinical utility is, however, limited to liquid chromatography users.
机译:审查目的:目的是突出临床环境中维生素D状况评估的新方面和方法学发展。最近的发现:维生素D状况评估的最新进展主要涉及两个领域:对其他循环中的维生素D代谢物[即, 3-epimer和24,25-(OH)2 D],为健康和疾病中维生素D代谢物谱分析以及方法学改进(包括开发参考测量程序,标准参考材料的认证,开发和开发)开辟了新的前景。标准化协议的应用以及将维生素D外部质量保证调查(DEQAS)更改为基于准确性的能力验证计划。摘要:尽管过去几年间方法和实验室之间的分析不精确性有所改善,但报告的给定人群中维生素D缺乏症的患病率仍取决于所使用的方法。但是,质量控制程序的改进将提高方法的标准化,准确性和可比性。目前,其他循环维生素D代谢产物(维生素D轮廓分析)及其临床实用性的分析评估仅限于液相色谱用户。

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