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采用 H NMR 光谱法在多实验室试验中对人血清和血浆中的定量脂蛋白亚类和低分子量代谢产物进行分析。

Quantitative Lipoprotein Subclass and Low Molecular Weight Metabolite Analysis in Human Serum and Plasma by H NMR Spectroscopy in a Multilaboratory Trial.

机构信息

The Imperial Clinical Phenotyping Centre, Division of Integrative Systems Medicine and Digestive Disease, Department of Surgery and Cancer , QEQM Building, Saint Mary's Hospital , London W2 1NY , United Kingdom.

Phenome Centre Birmingham , University of Birmingham , Edgbaston, Birmingham B15 2TT , United Kingdom.

出版信息

Anal Chem. 2018 Oct 16;90(20):11962-11971. doi: 10.1021/acs.analchem.8b02412. Epub 2018 Sep 27.

DOI:10.1021/acs.analchem.8b02412
PMID:30211542
Abstract

We report an extensive 600 MHz NMR trial of quantitative lipoprotein and small-molecule measurements in human blood serum and plasma. Five centers with eleven 600 MHz NMR spectrometers were used to analyze 98 samples including 20 quality controls (QCs), 37 commercially sourced, paired serum and plasma samples, and two National Institute of Science and Technology (NIST) reference material 1951c replicates. Samples were analyzed using rigorous protocols for sample preparation and experimental acquisition. A commercial lipoprotein subclass analysis was used to quantify 105 lipoprotein subclasses and 24 low molecular weight metabolites from the NMR spectra. For all spectrometers, the instrument specific variance in measuring internal QCs was lower than the percentage described by the National Cholesterol Education Program (NCEP) criteria for lipid testing [triglycerides <2.7%; cholesterol <2.8%; low-density lipoprotein (LDL) cholesterol <2.8%; high-density lipoprotein (HDL) cholesterol <2.3%], showing exceptional reproducibility for direct quantitation of lipoproteins in both matrixes. The average relative standard deviations (RSDs) for the 105 lipoprotein parameters in the 11 instruments were 4.6% and 3.9% for the two NIST samples, whereas they were 38% and 40% for the 37 commercially sourced plasmas and sera, respectively, showing negligible analytical compared to biological variation. The coefficient of variance (CV) obtained for the quantification of the small molecules across the 11 spectrometers was below 15% for 20 out of the 24 metabolites analyzed. This study provides further evidence of the suitability of NMR for high-throughput lipoprotein subcomponent analysis and small-molecule quantitation with the exceptional required reproducibility for clinical and other regulatory settings.

摘要

我们报告了一项广泛的 600MHz NMR 试验,用于定量测定人血清和血浆中的脂蛋白和小分子。五个中心的 11 台 600MHz NMR 光谱仪用于分析 98 个样本,包括 20 个质控品(QC)、37 个商业来源的配对血清和血浆样本以及两个美国国家标准与技术研究院(NIST)参考物质 1951c 的重复样本。样本使用严格的样本制备和实验采集方案进行分析。商业脂蛋白亚类分析用于从 NMR 光谱中定量 105 种脂蛋白亚类和 24 种低分子量代谢物。对于所有光谱仪,测量内部 QC 的仪器特定方差均低于国家胆固醇教育计划(NCEP)脂质测试标准所描述的百分比[甘油三酯 <2.7%;胆固醇 <2.8%;低密度脂蛋白(LDL)胆固醇 <2.8%;高密度脂蛋白(HDL)胆固醇 <2.3%],显示出在两种基质中直接定量脂蛋白的出色重现性。11 台仪器中 105 种脂蛋白参数的平均相对标准偏差(RSD)在两个 NIST 样本中分别为 4.6%和 3.9%,而在 37 个商业来源的血浆和血清中分别为 38%和 40%,表明与生物学变异相比,分析变异可忽略不计。在 11 台光谱仪中,24 种代谢物中有 20 种的小分子定量得到的变异系数(CV)低于 15%。本研究进一步证明了 NMR 适用于高通量脂蛋白亚组分分析和小分子定量,具有临床和其他监管环境所需的出色重现性。

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