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新生儿早发性败血症的脑血流和血清神经元特异性烯醇化酶。

Cerebral blood flow and serum neuron-specific enolase in early-onset neonatal sepsis.

机构信息

Departments of Pediatrics, Ain Shams University, Cairo, Egypt.

Radiodiagnosis, Ain Shams University, Cairo, Egypt.

出版信息

Pediatr Res. 2018 Aug;84(2):261-266. doi: 10.1038/s41390-018-0062-4. Epub 2018 May 26.

DOI:10.1038/s41390-018-0062-4
PMID:29907848
Abstract

BACKGROUND AND OBJECTIVES

Sepsis leads to systemic inflammatory response with cerebral blood flow (CBF) alteration and blood-brain barrier disruption that contribute to sepsis-associated encephalopathy (SAE). We aimed to evaluate cord blood neuron-specific enolase (cNSE) and CBF in early-onset neonatal sepsis (EONS) as predictors of SAE and to define short-term neurodevelopmental outcomes among survivors.

METHODS

cNSE was measured in 200 neonates with antenatal risk factors for EONS, stratified into two groups: sepsis (n = 96) and no-sepsis (n = 104). Trans-cranial Doppler of peak systolic velocities (PSV), end diastolic velocities (EDV) and resistive indices (RI) of anterior (ACA) and middle (MCA) cerebral arteries recorded on day 1 postnatal. Griffiths mental developmental scale (GMDS) was assessed at 6 months.

RESULTS

Increased cNSE, PSV, EDV, and decreased RI of both ACA and MCA were found in sepsis group compared to no-sepsis group (p < 0.001 for all). Patients with SAE (n = 34) had higher NSE, PSV, and EDV as well as lower RI of ACA and MCA compared to those without (p < 0.01 for all). SAE neonates had lower GMDS than those without. ACA RI of ≤0.61 was the best predictor of SAE.

CONCLUSION

High CBF and cNSE could be useful markers for prediction of SAE. SAE impairs neurodevelopmental scales at 6 months.

摘要

背景与目的

败血症会导致全身炎症反应,引起脑血流(CBF)改变和血脑屏障破坏,从而导致败血症相关性脑病(SAE)。我们旨在评估早期新生儿败血症(EONS)中脐血神经元特异性烯醇化酶(cNSE)和 CBF 作为 SAE 的预测指标,并定义幸存者的短期神经发育结局。

方法

对 200 例有 EONS 产前危险因素的新生儿进行 cNSE 测量,分为败血症组(n=96)和非败血症组(n=104)。在出生后第 1 天记录前(ACA)和中(MCA)脑动脉的收缩期峰值速度(PSV)、舒张末期速度(EDV)和阻力指数(RI)的经颅多普勒。在 6 个月时使用 Griffiths 精神发育量表(GMDS)进行评估。

结果

与非败血症组相比,败血症组的 cNSE、PSV、EDV 升高,ACA 和 MCA 的 RI 降低(所有 p<0.001)。与无 SAE 的患者相比,患有 SAE(n=34)的患者的 NSE、PSV 和 EDV 更高,ACA 和 MCA 的 RI 更低(所有 p<0.01)。SAE 新生儿的 GMDS 评分低于无 SAE 的新生儿。ACA RI≤0.61 是 SAE 的最佳预测指标。

结论

高 CBF 和 cNSE 可能是预测 SAE 的有用标志物。SAE 会在 6 个月时损害神经发育量表。

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