Florida Atlantic University, College of Medicine, 777 Glades Road, Boca Raton, FL 33431, USA.
Department of Biology, Charles E. Schmidt College of Science, Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431, USA.
Clin Neurol Neurosurg. 2020 Jun;193:105772. doi: 10.1016/j.clineuro.2020.105772. Epub 2020 Mar 3.
The brain's inflammatory reaction to traumatic brain injury (TBI) generally peaks between 24 and 48 h after injury. This inflammatory cascade can be neuroprotective or may mediate secondary brain injury beyond the initial TBI. Therefore, circulating inflammatory markers may be useful for predicting outcomes in pediatric TBI. The goal of this study was to determine whether elevations in peripheral blood neutrophil-to-lymphocyte ratios (NLRs) are associated with adverse outcomes in pediatric TBI patients.
188 pediatric patients (0-18 years) presenting to our institution with TBI from 2007 to 2017 were retrospectively reviewed. Absolute neutrophil and lymphocyte counts from a complete blood count (CBC) were used to calculate NLRs on admission (<12 h) and approximately 24, 48, and 72 h after injury. Data points included Glasgow Coma Scale (GCS) on admission, presence of post-traumatic amnesia (PTA), loss of consciousness (LOC), and Glasgow Outcome Scale Extended Pediatric Version (GOS-E Peds) with a median outcome span of 86 days.
A one-way ANOVA demonstrated statistically significant differences in NLR at 24 h (p = 0.004) and 48 h (p=0.003) among patients stratified by GOS-E Peds. No significant differences in NLR were observed at any time point based on GCS or PTA. Patients who experienced LOC had a significantly higher NLR on admission (p=0.013) and at 24 h (p<0.001) than those who did not.
In this study, relatively higher NLRs at 24 and 48 h post-TBI were associated with worse outcomes in pediatric patients. This suggests that NLR may be a useful and cost-effective outcome predictor in pediatric TBI as well as a possible future target for therapeutic intervention, warranting larger prospective trials.
颅脑创伤(TBI)后,大脑的炎症反应通常在损伤后 24 至 48 小时达到高峰。这种炎症级联反应可能具有神经保护作用,也可能介导初始 TBI 之外的继发性脑损伤。因此,循环炎症标志物可能有助于预测小儿 TBI 的结局。本研究旨在确定外周血中性粒细胞与淋巴细胞比值(NLR)升高是否与小儿 TBI 患者的不良结局相关。
回顾性分析了 2007 年至 2017 年期间我院收治的 188 例小儿 TBI 患者(0-18 岁)的临床资料。入院时(<12 小时)和伤后约 24、48 和 72 小时,采用全血细胞计数(CBC)计算 NLR。数据点包括入院时的格拉斯哥昏迷量表(GCS)、是否存在创伤后遗忘(PTA)、意识丧失(LOC)和扩展儿科格拉斯哥结局量表(GOS-E Peds),中位随访时间为 86 天。
单因素方差分析显示,根据 GOS-E Peds 分层,24 小时(p=0.004)和 48 小时(p=0.003)的 NLR 存在统计学差异。根据 GCS 或 PTA,NLR 在任何时间点均无显著差异。发生 LOC 的患者入院时(p=0.013)和 24 小时时(p<0.001)NLR 显著高于未发生 LOC 的患者。
在本研究中,TBI 后 24 和 48 小时相对较高的 NLR 与小儿患者的不良结局相关。这表明 NLR 可能是小儿 TBI 有用且具有成本效益的预后预测指标,也可能是未来治疗干预的潜在靶点,值得进一步开展前瞻性研究。