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快速高效的 LC-MS/MS 遗传性代谢紊乱诊断:尿液中有机酸、酰基甘氨酸和酰基肉碱分析的半自动化工作流程。

Rapid and efficient LC-MS/MS diagnosis of inherited metabolic disorders: a semi-automated workflow for analysis of organic acids, acylglycines, and acylcarnitines in urine.

机构信息

Faculty of Medicine and Dentistry, Palacký University Olomouc, Olomouc, Czech Republic.

Laboratory for Inherited Metabolic Disorders, Department of Clinical Biochemistry, University Hospital Olomouc, Olomouc, Czech Republic.

出版信息

Clin Chem Lab Med. 2023 May 19;61(11):2017-2027. doi: 10.1515/cclm-2023-0084. Print 2023 Oct 26.

Abstract

OBJECTIVES

The analysis of organic acids in urine is an important part of the diagnosis of inherited metabolic disorders (IMDs), for which gas chromatography coupled with mass spectrometry is still predominantly used.

METHODS

Ultra-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) assay for urinary organic acids, acylcarnitines and acylglycines was developed and validated. Sample preparation consists only of dilution and the addition of internal standards. Raw data processing is quick and easy using selective scheduled multiple reaction monitoring mode. A robust standardised value calculation as a data transformation together with advanced automatic visualisation tools are applied for easy evaluation of complex data.

RESULTS

The developed method covers 146 biomarkers consisting of organic acids (n=99), acylglycines (n=15) and acylcarnitines (n=32) including all clinically important isomeric compounds present. Linearity with r>0.98 for 118 analytes, inter-day accuracy between 80 and 120 % and imprecision under 15 % for 120 analytes were achieved. Over 2 years, more than 800 urine samples from children tested for IMDs were analysed. The workflow was evaluated on 93 patient samples and ERNDIM External Quality Assurance samples involving a total of 34 different IMDs.

CONCLUSIONS

The established LC-MS/MS workflow offers a comprehensive analysis of a wide range of organic acids, acylcarnitines and acylglycines in urine to perform effective, rapid and sensitive semi-automated diagnosis of more than 80 IMDs.

摘要

目的

尿液中有机酸的分析是遗传性代谢紊乱(IMD)诊断的重要组成部分,目前仍主要采用气相色谱-质谱联用技术进行分析。

方法

建立并验证了用于尿液有机酸、酰基肉碱和酰基甘氨酸分析的超高效液相色谱-串联质谱(LC-MS/MS)检测方法。样品制备仅需稀释并添加内标。采用选择性定时多重反应监测模式,可快速、轻松地进行原始数据处理。采用稳健的标准化值计算作为数据转换,并结合先进的自动可视化工具,便于对复杂数据进行评估。

结果

该方法涵盖了 146 种生物标志物,包括有机酸(n=99)、酰基甘氨酸(n=15)和酰基肉碱(n=32),其中包含所有具有临床重要性的同分异构体。118 种分析物的线性相关系数 r>0.98,120 种分析物的日内精密度为 80%至 120%,日间精密度<15%。2 年来,对 800 多份疑似 IMD 的儿童尿液样本进行了分析。该工作流程在 93 份患者样本和 ERNDIM 外部质量保证样本中进行了评估,共涉及 34 种不同的 IMD。

结论

所建立的 LC-MS/MS 工作流程可全面分析尿液中的多种有机酸、酰基肉碱和酰基甘氨酸,有效、快速、灵敏地进行 80 多种 IMD 的半自动诊断。

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