Mylemans Marnix, Nevejan Louis, Van Den Bremt Stefanie, Stubbe Muriel, Cruyssen Bert Vander, Moulakakis Christina, Berthold Heike, Konrad Christian, Bossuyt Xavier, Van Hoovels Lieve
Department of Laboratory Medicine, OLV Hospital, Aalst, Belgium.
Department of Rheumatology, OLV Hospital, Aalst, Belgium.
Clin Chim Acta. 2021 Jun;517:149-155. doi: 10.1016/j.cca.2021.02.022. Epub 2021 Mar 6.
Calprotectin (CLP) is a promising biomarker for the evaluation of neutrophil-related inflammation. Our aim was to establish reference values for circulating CLP in different sample types and to study the effect of pre-analytical variables.
Reference values were determined in 100 healthy individuals. Pre-analytical variables were evaluated in 10 healthy controls and four rheumatoid arthritis patients with active disease and covered sample type (serum with/without gel separator, heparin, EDTA and citrate plasma), pre-centrifugation time (<2 h, 6 h, 24 h), storage condition (2-8 °C, 18-25 °C, 30 °C) and storage time (24 h, 72 h, 7 days). CLP measurements were performed with the EliA™Calprotectin 2 assay on Phadia™200 (Thermo Fisher Scientific).
In healthy controls, baseline CLP concentrations in serum were more than double the concentration in EDTA and citrate plasma (0.909 µg/mL versus 0.259 µg/mL and 0.261 µg/mL respectively). Heparin, EDTA and citrate stabilized CLP concentrations for up to 6 h before centrifugation, whereas significant increases in CLP levels were observed when serum was left untreated during that time period.
Clinical studies on circulating CLP need to apply sample type-specific reference values and decision limits. To obtain reproducible CLP results in serum, more stringent pre-analytical sample handling instructions are needed.
钙卫蛋白(CLP)是一种用于评估中性粒细胞相关炎症的有前景的生物标志物。我们的目的是建立不同样本类型中循环CLP的参考值,并研究分析前变量的影响。
在100名健康个体中确定参考值。在10名健康对照者和4名患有活动性疾病的类风湿性关节炎患者中评估分析前变量,涵盖样本类型(含/不含凝胶分离器的血清、肝素、乙二胺四乙酸和枸橼酸盐血浆)、离心前时间(<2小时、6小时、24小时)、储存条件(2-8°C、18-25°C、30°C)和储存时间(24小时、72小时、7天)。使用Phadia™200(赛默飞世尔科技公司)上的EliA™钙卫蛋白2检测法进行CLP测量。
在健康对照者中,血清中的基线CLP浓度是乙二胺四乙酸和枸橼酸盐血浆中浓度的两倍多(分别为0.909μg/mL对0.259μg/mL和0.261μg/mL)。肝素、乙二胺四乙酸和枸橼酸盐在离心前长达6小时可稳定CLP浓度,而在此期间血清未处理时观察到CLP水平显著升高。
关于循环CLP的临床研究需要应用样本类型特异性的参考值和判定限。为了在血清中获得可重复的CLP结果,需要更严格的分析前样本处理说明。