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利用气相色谱-同位素稀释质谱法测定甘油空白甘油三酯浓度的方法。

A method for measuring glycerol-blanked triglyceride concentrations by using gas chromatography-isotope dilution mass spectrometry.

机构信息

Lipid Reference Laboratory, Department of Preventive Cardiology, National Cerebral and Cardiovascular Center, Osaka, Japan.

Public Health, Department of Social Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.

出版信息

Ann Clin Biochem. 2020 May;57(3):253-261. doi: 10.1177/0004563220921884. Epub 2020 Apr 27.

Abstract

BACKGROUND

Serum triglyceride concentrations are measured as total glycerides content in many Western countries. In Japan, glycerol-blanked triglycerides (TG-GB) are measured to identify postprandial hypertriglyceridaemia and to minimize the influence of glycerol formulation on serum triglyceride values. However, TG-GB measurements have not been standardized. Therefore, we developed an efficient quantification system for total glycerides and free glycerol that allows the calculation of TG-GB concentrations.

METHODS

We measured total glycerides and free glycerol in human serum by using gas chromatography-isotope dilution mass spectrometry and compared its performance to the reference method of the US Centers for Disease Control and Prevention (CDC).

RESULTS

Our practical method of total glycerides and free glycerol quantification achieved excellent precision for both within-run and among-run coefficients of variation (<1.5% and <2.7%, respectively), with an average recovery of 99.8% for free glycerol. However, we noted an average %bias of -0.26% for total glycerides and -3.15% for free glycerol between our TG-GB method and the CDC reference method.

CONCLUSIONS

This practical method of total glycerides and free glycerol quantification enables traceability assessment of TG-GB measurements. Differences between the output values of TG-GB and the CDC reference method might result from the differences in free glycerol values.

摘要

背景

在许多西方国家,血清甘油三酯浓度是通过测量总甘油含量来表示的。在日本,测定甘油空白甘油三酯(TG-GB)以识别餐后高甘油三酯血症,并最大程度地减少甘油制剂对血清甘油三酯值的影响。然而,TG-GB 的测量尚未标准化。因此,我们开发了一种用于总甘油和游离甘油的高效定量系统,可计算 TG-GB 浓度。

方法

我们使用气相色谱-同位素稀释质谱法测量了人血清中的总甘油和游离甘油,并将其性能与美国疾病控制与预防中心(CDC)的参考方法进行了比较。

结果

我们用于总甘油和游离甘油定量的实用方法在日内和日间变异系数方面均具有出色的精密度(分别<1.5%和<2.7%),游离甘油的平均回收率为 99.8%。但是,我们注意到我们的 TG-GB 方法与 CDC 参考方法之间总甘油的平均%偏差为-0.26%,游离甘油的平均%偏差为-3.15%。

结论

这种总甘油和游离甘油定量的实用方法可用于 TG-GB 测量的可追溯性评估。TG-GB 和 CDC 参考方法之间的输出值差异可能是由于游离甘油值的差异所致。

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