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用于血液样本分析前质量控制的临床生物标志物的鉴定。

Identification of clinical biomarkers for pre-analytical quality control of blood samples.

作者信息

Kang Hyun Ju, Jeon Soon Young, Park Jae-Sun, Yun Ji Young, Kil Han Na, Hong Won Kyung, Lee Mee-Hee, Kim Jun-Woo, Jeon Jae-Pil, Han Bok Ghee

出版信息

Biopreserv Biobank. 2013 Apr;11(2):94-100. doi: 10.1089/bio.2012.0051.

Abstract

BACKGROUND

Pre-analytical conditions are key factors in maintaining the high quality of biospecimens. They are necessary for accurate reproducibility of experiments in the field of biomarker discovery as well as achieving optimal specificity of laboratory tests for clinical diagnosis. In research at the National Biobank of Korea, we evaluated the impact of pre-analytical conditions on the stability of biobanked blood samples by measuring biochemical analytes commonly used in clinical laboratory tests.

METHODS

We measured 10 routine laboratory analytes in serum and plasma samples from healthy donors (n = 50) with a chemistry autoanalyzer (Hitachi 7600-110). The analyte measurements were made at different time courses based on delay of blood fractionation, freezing delay of fractionated serum and plasma samples, and at different cycles (0, 1, 3, 6, 9) of freeze-thawing. Statistically significant changes from the reference sample mean were determined using the repeated-measures ANOVA and the significant change limit (SCL).

RESULTS

The serum levels of GGT and LDH were changed significantly depending on both the time interval between blood collection and fractionation and the time interval between fractionation and freezing of serum and plasma samples. The glucose level was most sensitive only to the elapsed time between blood collection and centrifugation for blood fractionation. Based on these findings, a simple formula (glucose decrease by 1.387 mg/dL per hour) was derived to estimate the length of time delay after blood collection. In addition, AST, BUN, GGT, and LDH showed sensitive responses to repeated freeze-thaw cycles of serum and plasma samples.

CONCLUSION

These results suggest that GGT and LDH measurements can be used as quality control markers for certain pre-analytical conditions (eg, delayed processing or repeated freeze-thawing) of blood samples which are either directly used in the laboratory tests or stored for future research in the biobank.

摘要

背景

分析前条件是维持生物样本高质量的关键因素。对于生物标志物发现领域实验的准确可重复性以及实现临床诊断实验室检测的最佳特异性而言,这些条件必不可少。在韩国国家生物样本库的研究中,我们通过测量临床实验室检测中常用的生化分析物,评估了分析前条件对生物样本库血液样本稳定性的影响。

方法

我们使用化学自动分析仪(日立7600 - 110)对50名健康供体的血清和血浆样本中的10种常规实验室分析物进行了测量。根据血液分离延迟、分离后的血清和血浆样本冷冻延迟以及不同冻融循环次数(0、1、3、6、9次),在不同时间点进行分析物测量。使用重复测量方差分析和显著变化极限(SCL)确定与参考样本均值相比具有统计学显著差异的变化。

结果

γ-谷氨酰转移酶(GGT)和乳酸脱氢酶(LDH)的血清水平根据采血与分离之间的时间间隔以及血清和血浆样本分离与冷冻之间的时间间隔而发生显著变化。葡萄糖水平仅对采血与血液分离离心之间的 elapsed 时间最为敏感。基于这些发现,得出了一个简单公式(每小时葡萄糖降低1.387mg/dL)来估计采血后的延迟时间长度。此外,天门冬氨酸氨基转移酶(AST)、血尿素氮(BUN)、GGT和LDH对血清和血浆样本的重复冻融循环表现出敏感反应。

结论

这些结果表明,GGT和LDH测量可作为血液样本某些分析前条件(如处理延迟或重复冻融)的质量控制标志物,这些血液样本可直接用于实验室检测或存储在生物样本库中以供未来研究。

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