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Development of an isotope dilution mass spectrometry assay for HbA1c based on enzyme-cleaved peptide analysis

机译:基于酶切肽分析的HbA1c同位素稀释质谱分析方法的建立

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摘要

HbA1c is an index of control in diabetes patients. We report a highly reproducible measurement method for HbA1c based on analysis of the enzyme-cleaved peptide by electrospray ionization mass spectrometry using deuterium-labeled synthetic peptides as internal standards. Intra- and inter-assay coefficients of variation for the novel method ranged from 1.23 to 1.99% for samples with high and low HbA1c. Using this method, we clarified the extent of discrepancies among the indices of diabetes measured by conventional methods and the ESI method for clinical samples including those from patients with Hb variants. High-performance liquid chromatography (HPLC) methods for most samples with variants underestimate the true HbA1c value, although a few variants give a positive error for HbA1c. Immunoassays may also underestimate the values, if the reactivity of the antibody is low against the glycated N-terminal of the variant β-chains by conformational change. The method proposed here is an important step to establish a candidate definitive method, and is also useful in assessing specific HbA1c test systems using samples containing Hb variants.
机译:HbA1c是糖尿病患者控制指标。我们报告了一种高度可重复的HbA1c测量方法,该方法基于使用氘标记的合成肽作为内标物的电喷雾电离质谱对酶切肽的分析。对于HbA1c高和低的样品,新方法的测定内和测定间变异系数在1.23%至1.99%之间。使用这种方法,我们澄清了通过常规方法和ESI方法测量的临床样本(包括来自Hb变异患者的样本)的糖尿病指标之间的差异程度。大多数变体样品的高效液相色谱(HPLC)方法都低估了真实的HbA1c值,尽管一些变体给出了HbA1c的正误差。如果抗体通过构象变化对变体β链糖基化N端的反应性很低,则免疫测定法也可能会低估这些值。本文提出的方法是建立候选确定方法的重要步骤,并且在使用包含Hb变异体的样品评估特定的HbA1c测试系统中也很有用。

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