Lomholt Anne F, Frederiksen Camilla B, Christensen Ib J, Brünner Nils, Nielsen Hans J
Department of Surgical Gastroenterology, 435, Hvidovre University Hospital, Kettegaards Allé 30, DK-2650 Hvidovre, Denmark.
Clin Chim Acta. 2007 May 1;380(1-2):128-32. doi: 10.1016/j.cca.2007.01.022. Epub 2007 Feb 1.
Tissue Inhibitor of Metalloproteinases-1 (TIMP-1) may be a valuable biological marker in Colorectal Cancer (CRC). However, prospective validation of TIMP-1 as a biological marker should include a series of pre-analytical considerations. TIMP-1 is stored in platelets, which may degranulate during collection and storage. The aim of this study was to evaluate the influence of platelet TIMP-1 contamination on plasma TIMP-1 levels in healthy volunteers.
All four parts of this study were done on EDTA-plasma. 1: The effect of stasis was evaluated in plasma collected with and without tourniquet. The collected whole blood was centrifuged at three different g-values. The effect of cellular contamination was evaluated 2: by adding plasma from just above the buffy-coat to one of four tubes containing plasma from the same sample and 3: by separating the plasma into three layers: upper, middle and lower. 4: The effect of temperature was studied by collection and handling of corresponding samples on ice and at room temperature. Prior to analysis samples were stored at -80 degrees C. TIMP-1 was determined using a validated in-house ELISA.
1: TIMP-1 levels in plasma collected with or without stasis were not significantly different. Similarly TIMP-1 levels were not affected by the studied differences in centrifugation force. 2: TIMP-1 levels were significantly increased in plasma potentially contaminated with platelets (p<0.0001). 3: Separation of plasma into an upper, middle and lower layer did not affect the levels of plasma TIMP-1. 4: Samples kept at room temperature following collection showed significantly higher plasma TIMP-1 levels than samples kept on ice (p<0.0001).
Contamination with platelets during handling and storage of plasma may have significant effect on TIMP-1 levels. The results can define a standard operating procedure for sample collection and handling, which is important in obtaining uniform, comparable and reproducible plasma TIMP-1 levels.
基质金属蛋白酶-1组织抑制剂(TIMP-1)可能是结直肠癌(CRC)中有价值的生物标志物。然而,将TIMP-1作为生物标志物进行前瞻性验证应包括一系列分析前的考虑因素。TIMP-1储存在血小板中,血小板在采集和储存过程中可能会脱颗粒。本研究的目的是评估健康志愿者中血小板TIMP-1污染对血浆TIMP-1水平的影响。
本研究的所有四个部分均在乙二胺四乙酸(EDTA)血浆上进行。1:评估了使用止血带和不使用止血带采集的血浆中淤血的影响。采集的全血在三种不同的离心力值下离心。2:通过将白膜上方的血浆添加到四个装有同一样品血浆的试管之一中来评估细胞污染的影响,3:通过将血浆分离为三层:上层、中层和下层来评估。4:通过在冰上和室温下采集和处理相应样品来研究温度的影响。分析前样品储存在-80℃。使用经过验证的内部酶联免疫吸附测定(ELISA)法测定TIMP-1。
1:使用或不使用淤血采集的血浆中TIMP-1水平无显著差异。同样,TIMP-1水平不受所研究的离心力差异的影响。2:可能被血小板污染的血浆中TIMP-1水平显著升高(p<0.0001)。3:将血浆分离为上层、中层和下层不会影响血浆TIMP-1水平。4:采集后保存在室温下的样品血浆TIMP-1水平显著高于保存在冰上的样品(p<0.0001)。
血浆处理和储存过程中血小板污染可能对TIMP-1水平有显著影响。这些结果可以确定样品采集和处理的标准操作程序,这对于获得均匀、可比和可重复的血浆TIMP-1水平很重要。