外周血单核细胞髓样分化因子88与Toll样受体4在早产儿窒息后多器官功能障碍综合征中的表达及其意义

田渤, 赵凯红, 赵怡然, 付洪涛

中国儿童保健杂志 ›› 2022, Vol. 30 ›› Issue (4) : 454-457.

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中国儿童保健杂志 ›› 2022, Vol. 30 ›› Issue (4) : 454-457. DOI: 10.11852/zgetbjzz2021-0518
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外周血单核细胞髓样分化因子88与Toll样受体4在早产儿窒息后多器官功能障碍综合征中的表达及其意义

  • 田渤, 赵凯红, 赵怡然, 付洪涛
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Expression and its significance of peripheral blood mononuclear cells myeloid differentiation factor 88 and Toll-like receptor 4 in multiple organ dysfunction syndrome after asphyxia in premature infants

  • TIAN Bo, ZHAO Kai-hong, ZHAO Yi-ran, FU Hong-tao
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摘要

目的 探讨外周血单核细胞髓样分化因子88(My D88)与Toll样受体4(TLR4)在早产儿窒息后多器官功能障碍综合征(MODS)中的表达,为早产儿窒息后MODS的早期诊断及预后评估提供新思路。方法 连续性纳入2019年1月-2020年12月唐山市妇幼保健院新生儿科收治的115例窒息早产儿进行前瞻性研究,按照1 min Apgar评分将窒息早产儿分为轻度窒息组(n=70)与重度窒息组(n=45),以同期的50例健康早产儿作为对照组。比较3组早产儿中MODS发生率、MODS病死率及单器官损害发生率,外周血单核细胞My D88 mRNA及蛋白与TLR4 mRNA及蛋白的表达水平。结果 重度窒息组、轻度窒息组与对照组的MODS发生率分别为73.33%、31.43%、6.00%,MODS病死率分别为24.44%、5.71%、0,3组间比较差异有统计学意义(χ2=47.845、16.978,P<0.001);重度窒息组与轻度窒息组的单器官损害发生率明显高于对照组(P<0.05),重度窒息组明显高于轻度窒息组(P<0.05);重度窒息组与轻度窒息组的My D88 mRNA及蛋白与TLR4 mRNA及蛋白均明显高于对照组,且重度窒息组明显高于轻度窒息组(F=4.251、4.804、4.772、4.690,P<0.001)。结论 早产儿窒息后MODS发生率、外周血单核细胞My D88与TLR4表达水平均明显增高,My D88与TLR4有望成为早产儿窒息后MODS的早期诊断及预后评估指标。

Abstract

Objective To discuss the expression of peripheral blood mononuclear cells myeloid differentiation factor 88(My D88) and Toll-like receptor 4(TLR4) in multiple organ dysfunction syndrome(MODS) after asphyxia in premature infants, in order to provide a new idea for the early diagnosis and prognosis evaluation of MODS after asphyxia in premature infants. Methods A prospective study was conducted on 115 cases of asphyxiated premature infants in Neonatology Department of Tangshan Maternal & Child Health Care Hospital from January 2019 to December 2020.According to 1 min Apgar scores, the asphyxiated premature infants were divided into mild asphyxia group (n=70) and severe asphyxia group (n=45).Meanwhile, 50 cases of healthy preterm infants were selected as the control group.The prevalence of MODS, the mortality of MODS and the incidence of single organ damage were compared among the three groups.The expression levels of My D88 mRNA and protein, TLR4 mRNA and protein were compared among three groups. Results The incidence rates of MODS in severe asphyxia group, mild asphyxia group and control group were 73.33%, 31.43% and 6.00%, respectively, and the mortality rates of MODS were 24.44%, 5.71% and 0, respectively.There were statistically significant differences in the incidence rate of MODS and the mortality rate of MODS among the three groups (χ2=47.845, 16.978, P<0.001).The incidence of single organ damage in severe asphyxia group and mild asphyxia group were significantly higher than that in control group (P<0.05), and the incidence of single organ damage in severe asphyxia group was significantly higher than that in mild asphyxia group (P<0.05).The expression levels of My D88 mRNA and protein, TLR4 mRNA and protein in severe asphyxia group and mild asphyxia group were significantly higher than those in control group, which were also significantly higher in severe asphyxia group than in mild asphyxia group (F=4.251, 4.804, 4.772, 4.690, P<0.001). Conclusions The incidence of MODS and the expression levels of peripheral blood mononuclear cells My D88 and TLR4 are significantly increased in asphyxiated premature infants.My D88 and TLR4 are expected to be indicators for early diagnosis and prognosis evaluation of MODS after asphyxia in premature infants.

关键词

早产儿 / 窒息 / 多器官功能障碍综合征 / 髓样分化因子88 / Toll样受体4

Key words

premature infants / asphyxia / multiple organ dysfunction syndrome / myeloid differentiation factor 88 / Toll-like receptor 4

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田渤, 赵凯红, 赵怡然, 付洪涛. 外周血单核细胞髓样分化因子88与Toll样受体4在早产儿窒息后多器官功能障碍综合征中的表达及其意义[J]. 中国儿童保健杂志. 2022, 30(4): 454-457 https://doi.org/10.11852/zgetbjzz2021-0518
TIAN Bo, ZHAO Kai-hong, ZHAO Yi-ran, FU Hong-tao. Expression and its significance of peripheral blood mononuclear cells myeloid differentiation factor 88 and Toll-like receptor 4 in multiple organ dysfunction syndrome after asphyxia in premature infants[J]. Chinese Journal of Child Health Care. 2022, 30(4): 454-457 https://doi.org/10.11852/zgetbjzz2021-0518
中图分类号: R722.6   

参考文献

[1] 范懿隽,程雁,王杨.早期新生儿死亡病因学研究进展[J].中国妇幼健康研究,2021,32(1):158-162.
[2] 虞人杰, 王俊怡, 刘淑芳, 等.新生儿窒息多器官损害的临床诊断标准[J].中华围产医学杂志, 2016, 19(4): 241-242.
[3] 冯琼,明静,李春蕾,等.新生儿窒息继发多器官损伤的高危因素分析[J].中国临床医生杂志,2020,48(2):232-235.
[4] 张小蕾.新生儿窒息的原因及窒息后并发多脏器损害的临床研究[J].中国医药指南, 2017, 15(19):75-76.
[5] 胡玉懿,陈朴.髓样分化因子88多态性的研究进展[J].检验医学,2020,35(4):380-386.
[6] 古丽白热木·玉素因,毛艳,刘燕,等.TLRs介导的炎症信号通路与变应性鼻炎发病机制研究进展[J].医学综述,2020,26(1):50-53,58.
[7] 张惠月.新生儿窒息后器官损害,高危因素及转归临床研究[D].福州:福建医科大学,2017.
[8] 张小蕾.新生儿窒息的原因及窒息后并发多脏器损害的临床研究[J].中国医药指南, 2017, 15(19):75-76.
[9] 王道,施晓波,陈建林.人髓样分化因子88的生物信息学分析[J].激光生物学报,2020,29(3):252-259.
[10] 胡玉懿,陈朴.髓样分化因子88多态性的研究进展[J].检验医学,2020,35(4):380-386.
[11] 鲍璐璐,崔立红.TLR4/MyD88/NF-κB信号通路的研究进展[J].胃肠病学和肝病学杂志,2019,28(5):568-572.
[12] Zhang RL,Guo R, Liu Q,et al.Selenium deficiency via the tlr4/trif/nf-κb signaling pathway leading to inflammatory injury in chicken spleen[J].Biol Trace Elem Res,2021,199(2):693-702.
[13] 张洋.早产儿窒息后Toll样受体4及髓样分化因子88表达变化在多器官功能障碍综合征中的意义[J/OL].临床检验杂志(电子版), 2019, 8(2):84.
[14] Ystgaard MB, Scheffler K, Suganthan R, et al.Neuromodulatory effect of NLRP3 and ASC in neonatal hypoxic ischemic encephalopathy[J].Neonatology, 2019, 115(4): 355-362.
[15] Herath KHINM,Kim HJ,Lee JH, et al.Agardh containing polyphenols attenuates particulate matter-induced inflammatory response by blocking TLR-mediated MYD88-dependent MAPK signaling pathway in MLE-12 cells[J].J Ethnopharmacol,2021,265:113340.
[16] Ye WL, Liu XR,Bai YP,et al.Sepsis activates the TLR4/MyD88 pathway in schwann cells to promote infiltration of macrophages, thereby impeding neuromuscular function[J].Shock, 2021,55(1):90-99.

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