Ahearne Caroline E, Chang Ruby Y, Walsh Brian H, Boylan Geraldine B, Murray Deirdre M
The Irish Centre for Foetal and Neonatal Translational Research (INFANT), University College Cork, Cork, Ireland.
Dev Neurosci. 2017;39(1-4):59-65. doi: 10.1159/000471508. Epub 2017 May 11.
Activation of the inflammatory pathway is increasingly recognized as an important mechanism of injury following neonatal asphyxia and encephalopathy. This process may contribute to the poor prognosis seen in some cases, despite therapeutic hypothermia. Our group has previously identified raised interleukin (IL)-6 and IL-16, measured in umbilical cord blood at birth, to be predictive of grade of hypoxic-ischaemic encephalopathy (HIE). Our aim in this study was to examine the ability of these cytokines to predict the 3-year neurodevelopmental outcome in the same cohort. As part of a prospective, longitudinal cohort study set in a single tertiary maternity unit, term infants with biochemical and clinical evidence of perinatal asphyxia were recruited at birth. Umbilical cord blood was collected and analyzed for IL-6 and IL-16 using a Luminex assay. The neurodevelopmental outcome of these infants was assessed at 3 years using the Bayley Scales of Infant and Toddler Development (Edition 3). Early cord blood measurement of IL-6 and IL-16 and long-term outcome were available in 33/69 infants. Median (IQR) IL-16 differentiated infants with a severely abnormal outcome (n = 6) compared to all others (n = 27), (646 [466-1,085] vs. 383.5 [284-494] pg/mL; p = 0.012). IL-16 levels were able to predict a severe outcome with an area under the receiver-operating characteristic (ROC) curve of 0.827 (95% CI 0.628-1.000; p = 0.014). Levels ≥514 pg/mL predicted a severe outcome with a sensitivity of 83% and a specificity of 81%. IL-16 also outperformed other routine biochemical markers available at birth for the prediction of severe outcome. APGAR scores at 1 and 10 min were also predictive of a severe outcome (p = 0.022 and p = 0.036, respectively). A combination of IL-16 with these clinical markers did not improve predictive value, but IL-16 combined with electroencephalogram grading increased the area under the ROC curve. IL-6 did not show any association with 3-year outcome. This is the first report studying the association of IL-16 measured at birth with long-term outcome in a cohort of neonates with perinatal asphyxia. IL-16 may be an early biomarker of severe injury and aid in the long-term prognostication in infants with HIE.
炎症通路的激活日益被认为是新生儿窒息和脑病后损伤的重要机制。尽管采用了治疗性低温治疗,但这一过程可能导致某些病例预后不良。我们的研究小组之前已经确定,出生时脐血中白细胞介素(IL)-6和IL-16升高可预测缺氧缺血性脑病(HIE)的分级。本研究的目的是检验这些细胞因子预测同一队列中3岁神经发育结局的能力。作为在单一三级产科病房进行的一项前瞻性纵向队列研究的一部分,出生时招募了有围产期窒息生化和临床证据的足月儿。采集脐血,使用Luminex检测法分析IL-6和IL-16。使用贝利婴幼儿发育量表(第3版)在3岁时评估这些婴儿的神经发育结局。33/69例婴儿有出生时脐血IL-6和IL-16的早期测量值及长期结局数据。与所有其他婴儿(n = 27)相比,IL-16中位数(IQR)在结局严重异常的婴儿(n = 6)中存在差异,分别为646[466 - 1,085] pg/mL和383.5[284 - 494] pg/mL;p = 0.012。IL-16水平能够预测严重结局,受试者工作特征(ROC)曲线下面积为0.827(95%CI 0.628 - 1.000;p = 0.014)。≥514 pg/mL的水平预测严重结局的敏感性为83%,特异性为81%。IL-16在预测严重结局方面也优于出生时可用的其他常规生化标志物。1分钟和10分钟时的阿氏评分也可预测严重结局(分别为p = 0.022和p = 0.036)。IL-16与这些临床标志物联合使用并未提高预测价值,但IL-16与脑电图分级联合使用增加了ROC曲线下面积。IL-6与3岁结局未显示任何关联。这是第一项研究出生时测量的IL-16与围产期窒息新生儿队列长期结局之间关联的报告。IL-16可能是严重损伤的早期生物标志物,并有助于HIE婴儿的长期预后评估。