羊水中微核糖核酸-182表达与早产儿宫内感染和脑损伤的关系

张强, 卢红艳, 蒋峰, 王秋霞, 鞠慧敏

中国儿童保健杂志 ›› 2020, Vol. 28 ›› Issue (7) : 729-732.

PDF(535 KB)
PDF(535 KB)
中国儿童保健杂志 ›› 2020, Vol. 28 ›› Issue (7) : 729-732. DOI: 10.11852/zgetbjzz2019-1462
科研论著

羊水中微核糖核酸-182表达与早产儿宫内感染和脑损伤的关系

  • 张强, 卢红艳, 蒋峰, 王秋霞, 鞠慧敏
作者信息 +

Association of the expression of miR-182 in amniotic fluid with intrauterine infection and brain injury in premature infants

  • ZHANG Qiang, LU Hong-yan, JIANG Feng, WANG Qiu-xia, JU Hui-min
Author information +
文章历史 +

摘要

目的 分析羊水中微核糖核酸-182(miR-182)的表达与早产儿宫内感染和脑损伤的关系,为预测宫内感染后早产儿脑损伤的发生提供有效的预防方法。方法 选取2015年12月-2019年1月在江苏大学附属医院生产的125例胎龄小于34周单胎早产儿进行研究,在孕妇分娩时留取10 ml羊水,酶联免疫吸附实验(ELISA)检测羊水中肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β)、白细胞介素10(IL-10)、转化生长因子β(TGF-β)、白细胞介素8(IL-8)含量,实时定量PCR检测羊水中miR-182表达。胎盘行病理检查,判断是否存在绒毛膜羊膜炎,早产儿进行头颅影像学检查以诊断脑损伤。基于临床绒毛膜羊膜炎,将所有病例分为宫内感染组和无宫内感染组。结果 宫内感染组60例,其中发生脑损伤20例(33%);无宫内感染组65例,其中发生脑损伤10例(15%)。宫内感染组羊水中除IL-10降低外,IL-1β、TNF-α、TGF-β、IL-8及miR-182表达量均较无宫内感染组明显升高(t=8.04、17.23、17.37、15.56、4.90、18.13,P<0.001)。宫内感染组中合并脑损伤和无宫内感染组中合并脑损伤的羊水中miR-182表达量均较无脑损伤的明显上升(t=14.41、16.39,P<0.05)。结论 羊水中miR-182的表达与羊水中炎症细胞因子有协同作用,初步推测对早产儿宫内感染和脑损伤有促进作用,可联合细胞因子预测宫内感染后早产儿脑损伤。

Abstract

Objective To study the association of the expression of micro-ribonucleic acid-182(miR-182) in amniotic fluid with intrauterine infection and brain injury in premature infants,in order to provide reference for predicting the occurrence of brain injury in preterm infants after intrauterine infection. Methods Totally 125 singleton infants with gestational age less than 34 weeks were included in this study in Affiliated Hospital of Jiangsu University from December 2015 to January 2019.10 ml amniotic fluid was collected by pregnant women at birth for pathological diagnosis.The contents of TNF-α,IL-1β,IL-10,TGF-β and IL-8 in amniotic fluid were detected by enzyme-linked immunosorbent assay.The expression of miR-182 in amniotic fluid was detected by real-time quantitative PCR.Placenta was examined by pathology to determine the presence of chorioamnionitis.All premature infants conducted brain imaging to detect brain damage at the right timing.All cases were divided into intrauterine infection group and non-intrauterine infection group according to clinical chorioamnionitis result. Results There were 60 cases in intrauterine infection group,including 20 cases (33%) with brain injury.And 65 cases were in non-intrauterine infection group,including 10 cases (15%) with brain injury.The levels of IL-1β,TNF-α,TGF-β,IL-8 and miR-182 in intrauterine infection group were significantly higher than that in non-intrauterine infection group except from IL-10 (t=8.04,17.23,17.37,15.56,4.90,18.13,P<0.001).The expression of miR-182 in amniotic fluid was significantly higher in intrauterine infection group combined with brain injury than that without brain infection,which was also higher in non-intrauterine infection group combined with brain injury(t=14.41,16.39,P<0.05). Conclusion s The expression of miR-182 in amniotic fluid has synergistic effect with inflammatory cytokines in amniotic fluid.It is presumed that miR-182 in amniotic fluid can promote intrauterine infection and brain injury in premature infants,and can also predict brain damage in preterm infants after intrauterine infection when combined with cytokines.

关键词

羊水 / miR-182 / 早产儿 / 宫内感染 / 脑损伤

Key words

amniotic fluid / miR-182 / premature infants / intrauterine infection / brain injury

引用本文

导出引用
张强, 卢红艳, 蒋峰, 王秋霞, 鞠慧敏. 羊水中微核糖核酸-182表达与早产儿宫内感染和脑损伤的关系[J]. 中国儿童保健杂志. 2020, 28(7): 729-732 https://doi.org/10.11852/zgetbjzz2019-1462
ZHANG Qiang, LU Hong-yan, JIANG Feng, WANG Qiu-xia, JU Hui-min. Association of the expression of miR-182 in amniotic fluid with intrauterine infection and brain injury in premature infants[J]. Chinese Journal of Child Health Care. 2020, 28(7): 729-732 https://doi.org/10.11852/zgetbjzz2019-1462
中图分类号: R722.6   

参考文献

[1] Pugni L,Pietrasanta C,Acaia B,et al.Chorioamnionitis and neonatal outcome in preterm infants:a clinical overview[J].Matern Fetal Neonatal Med,2016,29(9):1525-1529.
[2] Zanardo V,Vedovato S,Suppiej A,et al.Histological inflammatory responses in the placenta and early neonatal brain injury[J].Pediatr Dev Pathol,2010,11(5):350-354.
[3] Kelada S,Sethupathy P,Okoye IS,et al.miR-182 and miR-10a are key regulators of Treg specialisation and stability during Schistosome and Leishmania-associated inflammation[J].PLoS Pathogens,2013,9(6):e1003451.
[4] Ding X,Sun B,Huang J,et al.The role of miR-182 in regulating pineal CLOCK expression after hypoxia-ischemia brain injury in neonatal rats[J].Neurosci Lett,2015,591:75-80.
[5] Gao F,Jiang X,Li Q,et al.Association of miR-182 expression in amniotic fluid with intrauterine infection and brain injury in premature infants[J].Exp Ther Med,2018,16(3):1905-1909.
[6] 谢幸,孔北华,段涛.妇产科学[M].9版.北京:人民卫生出版社,2018:524-525.
[7] 刘敬,杨于嘉,封志纯.“早产儿脑损伤诊断与防治专家共识”解读[J].中国当代儿科杂志,2012,14(12):885-887.
[8] Paton MCB,McDonald CA,Allison BJ,et al.Perinatal brain injury as a consequence of preterm birth and intrauterine inflammation:designing targeted stem cell therapies[J].Front Neurosci,2017,11:200.
[9] Leviton A,Allred EN,Kuban KCK,et al.Microbiologic and histologic characteristics of the extremely preterm infant′s placenta predict white matter damage and later cerebral palsy the ELGAN study[J].Pediatr Res,2010,67(1):95-101.
[10] Mallard C,Tremblay ME,Vexler ZS.Microglia and neonatal brain injury[J].Neuroscience,2019,405:68-76.
[11] Kunze M,Klar M,Morfeld CA,et al.Cytokines in noninvasively obtained amniotic fluid as predictors of fetal inflammatory response syndrome[J].Am J Obstet Gynecol,2016,215(1):96-98.
[12] Lu HY,Zhang Q,Wang QX,et al.Contribution of histologic chorioamnionitis and fetal inflammatory response syndrome to increased risk of brain injury in infants with preterm premature rupture of membranes[J].Pediatr Neurol,2016,61:94-98.
[13] 张强,卢红艳,王金秀,等.胎盘炎症及胎儿炎症反应综合征与早产儿脑损伤的关系研究[J].中国当代儿科杂志,2015,17(3):217-221.
[14] Bonestroo HJ,Heijnen CJ,Groenendaal F,et al.Development of cerebral gray and white matter injury and cerebral inflammation over time after inflammatory perinatal asphyxia[J].Dev Neurosci,2015,37(1):78-94.
[15] Schmidt AF,Kannan PS,Chougnet CA,et al.Intra-amniotic LPS causes acute neuroinflammation in preterm rhesus macaques[J].Neuroinflammation,2016,13(1):238.
[16] 卢红艳,张强,常明,等.脐血及羊水生物学标志预测胎膜早破早产儿脑损伤的价值[J].中华实用儿科临床杂志,2016,31(6):452-456.
[17] Li X,Zhang X,Zhang Q,et al.miR-182 contributes to cell proliferation,invasion and tumor growth in colorectal cancer by targeting DAB2IP[J].Int J Biochem Cell Biol,2019,111:27-36.
[18] Li Y,Zhang H,Gong H,et al.miR-182 suppresses invadopodia formation and metastasis in non-small cell lung cancer by targeting cortactin gene[J].Exp Clin Cancer Res,2018,37(1):141.
[19] Jin Y,Zhang ZL,Huang Y,et al.MiR-182-5p inhibited proliferation and metastasis of colorectal cancer by targeting MTDH[J].Eur Rev Med Pharmacol Sci,2019,23(4):1494-1501.
[20] Hanke M,Hoefig K,Merz H,et al.A robust methodology to study urine microRNA as tumor marker:microRNA-126 and microRNA-182 are related to urinary bladder cancer[C].Urol Oncol,2010,28(6):655-661.
[21] Stitrich AB,Haftmann C,Sgouroudis E,et al.The microRNA miR-182 is induced by IL-2 and promotes clonal expansion of activated helper T lymphocytes[J].Nat Immunol,2010,11(11):1057-1062.
[22] Yi H,Huang Y,Yang F,et al.MicroRNA-182 aggravates cerebral ischemia injury by targeting inhibitory member of the ASPP family (iASPP)[J].Arch Biochem Biophys,2016,620:52-58.

基金

镇江市社会发展项目(SH2017009)

PDF(535 KB)

Accesses

Citation

Detail

段落导航
相关文章

/