Department of Neonatology, Handan Maternal and Child Health Care Hospital, Handan, Hebei Province, People's Republic of China.
Department of Neonatal Pathology, Handan Maternal and Child Health Care Hospital, Handan, Hebei Province, People's Republic of China.
Am J Perinatol. 2022 Sep;39(12):1367-1374. doi: 10.1055/s-0040-1722601. Epub 2021 Jan 17.
Multiple randomized controlled trials have shown that hypothermia is a safe and effective treatment for neonatal moderate or severe hypoxic-ischemic encephalopathy (HIE). The neuroprotective mechanisms of hypothermia need further study. The aim of this study was to investigate the effect of hypothermia on the serum levels of myelin basic protein (MBP) and tumor necrosis factor-α (TNF-α) as well as neurodevelopmental outcomes in neonatal HIE.
Eighty-five neonates with moderate-to-severe HIE were divided into a hypothermia group ( = 49) and a control group ( = 36). Serum levels of MBP and TNF-α within 6 hours after birth and after 3 days of treatment were determined by enzyme-linked immunosorbent assay, and neurodevelopmental outcome at the age of 12 to 15 months was assessed by using the Gesell development scale.
After 3 days of treatment, serum levels of MBP and TNF-α in the control group were not significantly different from levels before treatment ( > 0.05), and serum levels of MBP and TNF-α in the hypothermia group were significantly lower than levels before treatment ( < 0.05). Serum levels of MBP and TNF-α were significantly negatively correlated with developmental quotient (DQ; = - 0.7945, = 0.0000; = - 0.7035, = 0.0000, respectively). Serum levels of MBP and TNF-α in neurodevelopmentally impaired infants were significantly higher than those in infants with suspected neurodevelopmental impairment and those in neurodevelopmentally normal infants (both < 0.01). The rate of reduction of neurodevelopmental impairment was higher among infants in the hypothermia group than among those in the control group (χ = 16.3900, < 0.05).
Hypothermia can reduce serum levels of MBP and TNF-α in neonates with HIE. Inhibiting the release of TNF-α may be one of the mechanisms by which hypothermia protects the myelin sheath.
· Hypothermia can reduce serum levels of MBP and TNF-α in neonatal HIE.. · Hypothermia improves neurodevelopmental outcomes and reduces the rate of neurodevelopmental impairment.. · Hypothermia is a feasible and effective treatment for neonates with moderate or severe HIE..
多项随机对照试验表明,低温治疗是安全有效的新生儿中重度缺氧缺血性脑病(HIE)的治疗方法。低温的神经保护机制仍需进一步研究。本研究旨在探讨低温对新生儿 HIE 患者血清髓鞘碱性蛋白(MBP)和肿瘤坏死因子-α(TNF-α)水平及神经发育结局的影响。
将 85 例中重度 HIE 新生儿分为低温组(n=49)和对照组(n=36)。采用酶联免疫吸附试验测定两组患儿出生后 6 小时及治疗后 3 天血清 MBP 和 TNF-α水平,采用盖塞尔发育量表评估患儿 12~15 月龄时的神经发育结局。
治疗 3 天后,对照组患儿血清 MBP 和 TNF-α水平与治疗前比较差异无统计学意义(>0.05),低温组患儿血清 MBP 和 TNF-α水平均显著低于治疗前(<0.05)。血清 MBP 和 TNF-α水平与发育商(DQ)均呈显著负相关(r= -0.7945,P=0.0000;r= -0.7035,P=0.0000)。神经发育障碍患儿血清 MBP 和 TNF-α水平显著高于疑似神经发育障碍患儿和神经发育正常患儿(均<0.01)。低温组患儿神经发育障碍改善率高于对照组(χ²=16.3900,P<0.05)。
低温治疗可降低 HIE 新生儿血清 MBP 和 TNF-α水平。抑制 TNF-α释放可能是低温保护髓鞘的机制之一。
· 低温治疗可降低新生儿 HIE 患儿血清 MBP 和 TNF-α水平。· 低温治疗可改善神经发育结局,降低神经发育障碍发生率。· 低温治疗是中重度 HIE 新生儿可行有效的治疗方法。