Sapa Agnieszka, Rak Alina, Wybieralska Magdalena, Machoń Jakub, Krzywonos-Zawadzka Anna, Zawadzki Kamil, Wełna Marek, Woźniak Mieczysław
Department of Clinical Chemistry, Wroclaw Medical University, Poland.
Ziemo-Vita Public Health Care Laboratory Ltd., Wrocław, Poland.
Adv Clin Exp Med. 2017 Jan-Feb;26(1):101-108. doi: 10.17219/acem/63251.
Sepsis is one of the most common causes of hospitalization and it is characterized by a high mortality rate in spite of the great progress in diagnosis and treatment achieved in recent years. Early diagnosis of sepsis is one of the most important elements of effective treatment. The clinical symptoms are not specific and biomarkers are considered to be useful tools in sepsis diagnostics.
The aim of our study was to evaluate the diagnostic value of sCD163 as a marker of sepsis and a comparison of it with procalcitonin and neopterin in ICU patients.
Concentrations of PCT, sCD163 and NPT were measured in 52 serum samples collected from 30 patients of the Department of Anesthesiology and Intensive Therapy of the University Hospital in Wroclaw. Venous blood was collected on the 1st and 3rd day of hospitalization. The Human CD163 Quantikine ELISA Kit was used to determine the concentrations of sCD163. Neopterin concentrations were measured by a Neopterin ELISA kit. PCT was measured at the University Center of Laboratory Diagnostics in Wroclaw using an automatic VIDAS® B.R.A.H.M.S. PCT assay.
Our study showed that there was a significant difference between the values obtained in the study and the reference group for PCT (p < 0.0001), sCD163 (p = 0.0001) and NPT (p = 0.0001), whereas there was no difference observed between the samples obtained on the 1st and 3rd day (p = 0.5129). The area under the ROC curve was 0.847, and was comparable to the AUC of procalcitonin (0.840), and slightly higher than the AUC of neopterin (0.763), although these differences were not significant (p = 0.2990 and p = 0.9329, respectively).
sCD163 and neopterin are promising parameters in the diagnosis of sepsis, and their value in the diagnosis of sepsis in critically ill patients may be comparable to procalcitonin.
脓毒症是住院治疗的最常见病因之一,尽管近年来在诊断和治疗方面取得了巨大进展,但其死亡率仍然很高。脓毒症的早期诊断是有效治疗的最重要环节之一。临床症状不具有特异性,生物标志物被认为是脓毒症诊断的有用工具。
本研究旨在评估可溶性细胞间黏附分子-163(sCD163)作为脓毒症标志物的诊断价值,并将其与降钙素原和蝶呤在重症监护病房(ICU)患者中的情况进行比较。
从弗罗茨瓦夫大学医院麻醉与重症治疗科的30例患者中采集了52份血清样本,检测其中降钙素原(PCT)、sCD163和蝶呤(NPT)的浓度。在住院第1天和第3天采集静脉血。使用人CD163定量酶联免疫吸附测定(ELISA)试剂盒测定sCD163的浓度。通过蝶呤ELISA试剂盒测定蝶呤浓度。在弗罗茨瓦夫大学实验室诊断中心使用自动VIDAS® B.R.A.H.M.S. PCT检测法测定PCT。
我们的研究表明,研究中获得的值与PCT(p < 0.0001)、sCD163(p = 0.0001)和NPT(p = 0.0001)的参考组之间存在显著差异,而在第1天和第3天获得的样本之间未观察到差异(p = 0.5129)。ROC曲线下面积为0.847,与降钙素原的AUC(0.840)相当,略高于蝶呤的AUC(0.763),尽管这些差异不显著(分别为p = 0.2990和p = 0.9329)。
sCD163和蝶呤是脓毒症诊断中有前景的参数,它们在危重症患者脓毒症诊断中的价值可能与降钙素原相当。