Dulay Antonette T, Buhimschi Irina A, Zhao Guomao, Bahtiyar Mert O, Thung Stephen F, Cackovic Michael, Buhimschi Catalin S
Department of Obstetrics & Gynecology, The Ohio State University College of Medicine, Columbus, OH 43210, United States; Center for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH 43215, United States.
Department of Obstetrics & Gynecology, The Ohio State University College of Medicine, Columbus, OH 43210, United States; Center for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH 43215, United States; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH 43215, United States.
Cytokine. 2015 Dec;76(2):236-243. doi: 10.1016/j.cyto.2015.04.014. Epub 2015 May 6.
The arsenal of maternal and amniotic fluid (AF) immune response to local or systemic infection includes among others the acute-phase reactants IL-6, C-Reactive Protein (CRP) and Procalcitonin (PCT). If these molecules can be used as non-invasive biomarkers of intra-amniotic infection (IAI) in the subclinical phase of the disease remains incompletely known.
We used time-matched maternal serum, urine and AF from 100 pregnant women who had an amniocentesis to rule out IAI in the setting of preterm labor, PPROM or systemic inflammatory response (SIR: pyelonephritis, appendicitis, pneumonia) to infection. Cord blood was analyzed in a subgroup of cases. We used sensitive immunoassays to quantify the levels of inflammatory markers in the maternal blood, urine and AF compartment. Microbiological testing and placental pathology was used to establish infection and histological chorioamnionitis.
PCT was not a useful biomarker of IAI in any of the studied compartments. Maternal blood IL-6 and CRP levels were elevated in women with subclinical IAI. Compared to clinically manifest chorioamnionitis group, women with SIR have higher maternal blood IL-6 levels rendering some marginal diagnostic benefit for this condition. Urine was not a useful biological sample for assessment of IAI using either of these three inflammatory biomarkers.
In women with subclinical IAI, the large overlapping confidence intervals and different cut-offs for the maternal blood levels of IL-6, CRP and PCT likely make interpretation of their absolute values difficult for clinical decision-making.
母体和羊水(AF)对局部或全身感染的免疫反应武器库包括急性期反应物白细胞介素-6(IL-6)、C反应蛋白(CRP)和降钙素原(PCT)等。这些分子是否可作为羊膜腔内感染(IAI)亚临床阶段的非侵入性生物标志物仍不完全清楚。
我们使用了100名接受羊膜腔穿刺术以排除早产、胎膜早破或全身炎症反应(SIR:肾盂肾炎、阑尾炎、肺炎)感染情况下IAI的孕妇的时间匹配的母体血清、尿液和羊水。在部分病例亚组中分析了脐血。我们使用敏感的免疫测定法来量化母体血液、尿液和羊水中炎症标志物的水平。微生物检测和胎盘病理学用于确定感染和组织学绒毛膜羊膜炎。
在任何研究的样本中,PCT都不是IAI的有用生物标志物。亚临床IAI女性的母体血液IL-6和CRP水平升高。与临床表现为绒毛膜羊膜炎的组相比,SIR女性的母体血液IL-6水平更高,这对该病症有一定的边际诊断益处。使用这三种炎症生物标志物中的任何一种,尿液都不是评估IAI的有用生物样本。
在亚临床IAI女性中,母体血液中IL-6、CRP和PCT水平的大的重叠置信区间和不同的临界值可能使其绝对值难以用于临床决策解释。