Lee Jae-Eun, Lee Jin-Hyun, Hong Maria, Park Seul-Ki, Yu Ji-In, Shin So-Youn, Kim Shine Young
National Biobank of Korea, Center for Genome Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju, Korea.
Department of Laboratory Medicine, Pusan National University School of Medicine, Busan, Korea.
Osong Public Health Res Perspect. 2016 Dec;7(6):351-355. doi: 10.1016/j.phrp.2016.11.004. Epub 2016 Nov 16.
Progastrin-releasing peptide (proGRP) is a promising biomarker for small cell lung cancer. However, not much is known about how sample processing and storage conditions affect the stability of proGRP. Here, we examined the effects of repeated freeze-thaw cycles on the stability of proGRP in plasma and serum.
Concentrations of proGRP were measured in plasma and serum samples exposed to two, three, or four freeze-thaw cycles and these were compared with values of corresponding samples exposed to one cycle (baseline). We also performed the area under the receiver-operating-characteristic curve (AUC) analysis to determine whether the differences of proGRP concentrations between each paired plasma and serum sample (ΔproGRP) can be used for identifying the samples that have been exposed to multiple freeze-thaw cycles.
Concentrations of proGRP gradually decreased in both plasma and serum samples with increasing numbers of freeze-thaw cycles. Reduction rates of proGRP concentrations were greater in serum than in plasma samples and serum proGRP levels declined with statistical significance ( < 0.001) up to 10.1% after four freeze-thaw cycles. The ΔproGRP measurement showed fair accuracy (AUC = 0.741) for identifying samples that had been through four freeze-thaw cycles. The sensitivity was 82.8% and specificity was 62.1% at an optimal cut-off point of > 4.9.
Our study shows that the stability of circulating proGRP is affected in both plasma and serum samples by repeated freezing and thawing. We also show that ΔproGRP could be used for identifying paired plasma and serum samples subjected to multiple freeze-thaw cycles.
胃泌素释放肽前体(proGRP)是小细胞肺癌一种很有前景的生物标志物。然而,关于样本处理和储存条件如何影响proGRP的稳定性,人们了解得并不多。在此,我们研究了反复冻融循环对血浆和血清中proGRP稳定性的影响。
测量血浆和血清样本在经历两次、三次或四次冻融循环后的proGRP浓度,并将其与经历一次循环(基线)的相应样本的值进行比较。我们还进行了受试者操作特征曲线(AUC)分析,以确定每对血浆和血清样本之间proGRP浓度的差异(ΔproGRP)是否可用于识别经历多次冻融循环的样本。
随着冻融循环次数的增加,血浆和血清样本中proGRP的浓度均逐渐降低。血清中proGRP浓度的降低率高于血浆样本,且在经历四次冻融循环后,血清proGRP水平下降具有统计学意义(<0.001),下降幅度高达10.1%。ΔproGRP测量对于识别经历四次冻融循环的样本显示出较好的准确性(AUC = 0.741)。在最佳截断点>4.9时,灵敏度为82.8%,特异性为62.1%。
我们的研究表明,反复冻融会影响血浆和血清样本中循环proGRP的稳定性。我们还表明,ΔproGRP可用于识别经历多次冻融循环的配对血浆和血清样本。