[Performance validation and consistency assessment of three liquid chromatography-tandem mass spectrometry methods for detecting fat-soluble vitamins].

Bing-Chu Li, Bing-Hui Li, Zhi-Yang Chen, Zi-Yang Li, Mei-Ling Yin, Xing Lyu, Zhong-Yuan Xiang, Qi-Chen Long, Min Hu
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Abstract

Accurate quantification of fat-soluble vitamin A (VA), vitamin D (25(OH)D), vitamin E (VE), vitamin K (VK) is essential for health assessment and disease diagnosis. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) plays a crucial role in the measurement of these vitamins due to its high specificity and sensitivity. However, the comparability and concordance of the detection results among different LC-MS/MS methods are still suboptimal. In this study, the analytical performance including linearity, limit of detection, limit of quantitation, precision, accuracy and carryover was evaluated according to CLSI C62 and the Suggestions on Clinical Application of Liquid Chromatography-Mass Spectrometry. Aliquots of 40 patient samples were collected from August to October 2022 from the Second Xiangya Hospital, Central South University. These fat-soluble vitamins were measured using three LC-MS/MS methods. Passing-Bablok regression, Bland-Altman plots and concordance correlation coefficient (CCC) were performed to compare the differences among three methods. The consistency of the results before and after recalibration with a unified calibrator was evaluated. The results showed that the total CVs for the three mass spectrometry kits were 2.7%-10.1%, and the recoveries for all kits ranged from 88.8% to 109.2%, indicating that their detection performance met the requirements for clinical application. Concordance correlation analysis showed that two of the three methods had substantial agreement in vitamin D testing (CCC: 0.938), while the CCCs for other methods ranged from 0.322 to 0.853. After recalibration with a unified calibrator, except for vitamin K, the CCCs for the results of the three methods ranged from 0.918 to 0.983. In conclusion, the performance validation results of three LC-MS/MS methods for fat-soluble vitamins meet clinical requirements. The consistency among the three methods was poor, but using a unified calibrator significantly improved the consistency of these methods. The study provides recommendations for the standardization of clinical fat-soluble vitamin testing, thereby contributing to improved accuracy and consistency of results. This study will provide more reliable evidence for clinical diagnosis and treatment.

Abstract Image

[三种液相色谱-串联质谱法检测脂溶性维生素的性能验证和一致性评估]。
脂溶性维生素A (VA)、维生素D (25(OH)D)、维生素E (VE)、维生素K (VK)的准确定量对健康评估和疾病诊断至关重要。液相色谱-串联质谱法(LC-MS/MS)由于其高特异性和高灵敏度,在这些维生素的测定中起着至关重要的作用。然而,不同LC-MS/MS方法检测结果的可比性和一致性仍不理想。本研究根据CLSI C62标准和《液相色谱-质谱联用技术临床应用建议》,评价了液相色谱-质谱联用技术的分析性能,包括线性度、检出限、定量限、精密度、准确度和结转率。于2022年8月至10月在中南大学湘雅第二医院采集40例患者样本。脂溶性维生素采用三种LC-MS/MS方法测定。采用pass - bablok回归、Bland-Altman图和一致性相关系数(CCC)比较三种方法的差异。用统一校准器重新校准前后结果的一致性进行了评价。结果表明,3种质谱试剂盒的总CVs为2.7% ~ 10.1%,加样回收率为88.8% ~ 109.2%,检测性能满足临床应用要求。一致性相关分析表明,3种方法中2种方法在维生素D检测中具有较强的一致性(CCC: 0.938),其他方法的CCC范围为0.322 ~ 0.853。用统一校定器重新校准后,除维生素K外,三种方法的CCCs范围为0.918 ~ 0.983。综上所述,3种脂溶性维生素的LC-MS/MS方法的性能验证结果均符合临床要求。三种方法的一致性较差,统一校准器的使用显著提高了三种方法的一致性。本研究为临床脂溶性维生素检测的标准化提供了建议,从而有助于提高结果的准确性和一致性。本研究将为临床诊断和治疗提供更可靠的依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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