|本期目录/Table of Contents|

[1]王 丽,杨素艳.血清BDNF在新生儿缺氧缺血性脑病亚低温治疗中的临床价值研究[J].天津医科大学学报,2024,30(02):157-161.[doi:10.20135/j.issn.1006-8147.2024.02.0157]
 WANG Li,YANG Suyan.Clinical value of serum BDNF in mild hypothermia treatment of neonatal hypoxic-ischemic encephalopathy[J].Journal of Tianjin Medical University,2024,30(02):157-161.[doi:10.20135/j.issn.1006-8147.2024.02.0157]
点击复制

血清BDNF在新生儿缺氧缺血性脑病亚低温治疗中的临床价值研究(PDF)
分享到:

《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
30卷
期数:
2024年02期
页码:
157-161
栏目:
临床医学
出版日期:
2024-03-20

文章信息/Info

Title:
Clinical value of serum BDNF in mild hypothermia treatment of neonatal hypoxic-ischemic encephalopathy
文章编号:
1006-8147(2024)02-0157-05
作者:
王 丽杨素艳
(天津医科大学第二医院产科,天津300211)
Author(s):
WANG LiYANG Suyan
(Department of Obstetric,the Second Hospital of Tianjin Medical University,Tianjin 300211,China)
关键词:
脑源性神经营养因子新生儿缺氧缺血性脑病亚低温治疗
Keywords:
brain-derived neurotrophic factor hypoxic-ischemic encephalopathy mild hypothermia therapy
分类号:
R722.1
DOI:
10.20135/j.issn.1006-8147.2024.02.0157
文献标志码:
A
摘要:
目的:探讨脑源性神经营养因子(BDNF)在新生儿缺氧缺血性脑病(HIE)亚低温治疗的临床价值。方法:选取2018年5月至2022年4月在天津医科大学第二医院新生儿科无HIE的20名健康婴儿为对照组,接受亚低温治疗的90例HIE患儿为研究组(中度HIE患儿48例,重度HIE患儿42例)。分别于治疗前(生后1 h)、治疗后第3天及第7天测定患儿BDNF、肌酸磷酸激酶(CK)和肌酸激酶同工酶MB(CK-MB)水平及治疗后第3天酸碱度(PH)值、碱剩余(BE)值。结果:BDNF在重度HIE患儿中水平显著高于中度组(t=8.56,P<0.01),中度和重度HIE患儿的亚低温疗效分别为95.8%和66.7%,亚低温治疗后神经异常组或死亡组BDNF水平明显高于改善组。对于中度HIE患儿,亚低温治疗后3 d和7 d与出生后1 h相比,血清CK-MB和CK水平均显著降低(F=66.35、87.06,均P<0.01);重度HIE患儿经亚低温治疗后表现出相同的趋势(F=79.23、138.2,均P<0.01)。对于PH和BE,中度HIE患儿治疗3 d均较生后1 h升高,差异有统计学意义(t=14.05、25.201,均P<0.01);重度HIE患儿治疗后表现出相同的变化趋势(t=16.783、29.17,均P<0.01)。结论:血清BDNF水平可能成为亚低温治疗HIE患儿临床效果新的预测指标。
Abstract:
Objective:To investigate the clinical value of brain-derived neurotrophic factor(BDNF) of neonatal hypoxic-ischemic encephalopathy(HIE) with mild hypothermia treatment. Methods:Twenty healthy infants without HIE in the Department of Neonatology, the Second Hospital of Tianjin Medical University from May 2018 to April 2022 were selected as the control group,and 90 infants with HIE receiving mild hypothermia treatment were selected as the study group,including 48 infants with moderate HIE and 42 infants with severe HIE. The levels of BDNF,creatine phosphokinase(CK) and creatine kinase isoenzyme MB(CK-MB) were measured before treatment(1 hour after birth),on the 3rd day and the 7th day after treatment,and the PH value and base residual(BE) value were measured on the 3rd day after treatment. Results:The level of BDNF in children with severe HIE was significantly higher than that in the moderate group(t=8.56,P<0.01),and the efficacy of mild hypothermia in children with moderate and severe HIE was 95.8% and 66.7%,respectively. After mild hypothermia,the level of BDNF in the neurologic abnormality group or death group was significantly higher than that in the improvement group. For children with moderate HIE,serum CK-MB and CK levels were significantly decreased at the 3rd and the 7th day after mild hypothermia treatment compared with 1 hour after birth(F=66.35,87.06,both P<0.01). The children with severe HIE showed the same trend after mild hypothermia treatment(F=79.23,138.2,both P<0.01). The level of PH and BE in children with moderate HIE was higher at the 3rd day after treatment than at 1 hour after birth,and the difference was statistically significant(t=14.05,25.201,both P<0.01). The children with severe HIE showed the same trend after treatment(t=16.783,29.17,both P<0.01). Conclusion:The level of serum BDNF may be a new predictor of clinical efficacy in mild hypothermia treatment of HIE infants.

参考文献/References:

[1] 孟卫霞,黄莉芬. 缺氧缺血性脑病患儿血流动力学及血清神经生长因子、髓磷脂碱性蛋白、脑钠肽水平变化[J]. 中国临床医生杂志,2017,45(2):100-102.
[2] 中华医学会儿科学分会新生儿学组,中华儿科杂志编辑委员会. 亚低温治疗新生儿缺氧缺血性脑病专家共识(2022)[J]. 中华儿科杂志,2022,60(10):983-989.
[3] ALMLI C R,LEVY T J,HAN B H,et al. BDNF protects against spatial memory deficits following neonatal hypoxia-ischemia[J]. Exper Neurol,2000,166(1):1-114.
[4] LIU F,YANG S,DU Z,et al. Dynamic changes of cerebral-specific proteins in full-term newborns with hypoxic-ischemic encephalopathy [J]. Cell Bioch Biophys,2013,66(2):389-396.
[5] 中华医学会儿科学分会新生儿学组. 新生儿缺氧缺血性脑病诊断标准 [J]. 中国当代儿科杂志,2005,7(2):97-98.
[6] 陈小娜,姜毅. 2018昆士兰临床指南:缺氧缺血性脑病介绍 [J]. 中华新生儿科杂志,2019,34(1):77-78.
[7] 卫生部新生儿疾病重点试验室,复旦大学附属儿科医院. 亚低温治疗新生儿缺氧缺血性脑病方案(2011)[J]. 中国循证儿科杂志,2011,6(5):337-339.
[8] 王卫平,孙锟,常立文. 儿科学[M]. 北京:人民卫生出版社(第9版),2021:101.
[9] SHANKARAN S,LAPTOOK A R,TYSON J E,et al. Evolution of encephalopathy during whole body hypothermia for neonatal hypoxic-ischemic encephalopathy[J]. J Pediatr,2012,160(4):567-572.
[10] 章六秀,彭运聪,杨林生,等. 中重度新生儿缺氧缺血性脑病亚低温治疗时机选择[J]. 现代仪器与医疗,2017,23(5):60-62.
[11] 穆艳顺.新生儿缺氧缺血性脑病神经标志物研究进展[J]. 中国医学创新,2021,18(11):185-188.
[12] 代云飞,王通通,马微,等. 神经生长因子、脑源性神经生长因子及其前体在神经系统中的效应[J]. 中国组织工程研究,2018,22(28):158-164.
[13] WANG L,KE J,LI Y,et al. Inhibition of miRNA-210 reverses nicotine-induced brain hypoxic-ischemic injury in neonatal rats[J]. Internat J Biol Sci,2017,13(1):76-84.
[14] DIAZ J,ABIOLA S,KIM N,et al. Therapeutic hypothermia provides variable protection against behavioral deficits after neonatal hypoxia-ischemia:a potential role for brain-derived neurotrophic factor [J]. Devel Neurosc,2017,39(1-4):257-272.
[15] SUN J,QU Y,HE H,et al. Protective effect of polydatin on learning and memory impairments in neonatal rats with hypoxicischemic brain injury by up-regulating brain-derived neurotrophic factor[J]. Mol Med Reports,2014,10(6):3047-3051.
[16] AN N,YVONNE W,THEO K,et al. Plasma biomarkers of brain injury in neonatal hypoxic-ischemic encephalopathy[J]. J Ped,2018, 194:67-75.
[17] SILVEIRA R C,PROCIANOY R S. Hypothermia therapy for newborns with hypoxic ischemic encephalopathy[J]. J Ped,2015,91(6):78-83.

相似文献/References:

[1]王菲,常光明,耿鑫.BDNF和TERT联合转染BMSCs对血管性痴呆大鼠学习记忆功能恢复及海马CA1区超微结构的影响[J].天津医科大学学报,2014,20(03):172.
 WANG Fei,CHANG Guang-ming,GENG Xin.BMSCs co-transfected with BDNF and TERT improve the ability of cognition and ultra-structure in the hippocampal CA1 region of the rats with vascular dementia[J].Journal of Tianjin Medical University,2014,20(02):172.

备注/Memo

备注/Memo:
基金项目 国家重点研发计划(2021YFC2009303)
作者简介 王丽(1982-),女,医师,学士,研究方向:胎儿超声,新生儿窒息;通信作者:杨素艳,E-mail:879588622@qq.com。
更新日期/Last Update: 2024-03-20