中性粒细胞明胶酶相关脂质运载蛋白、白细胞介素33、肿瘤坏死   因子α对非常早产儿支气管肺发育不良的早期预测作用

邹巧巧, 王慧琴

中国儿童保健杂志 ›› 2020, Vol. 28 ›› Issue (12) : 1389-1392.

PDF(500 KB)
PDF(500 KB)
中国儿童保健杂志 ›› 2020, Vol. 28 ›› Issue (12) : 1389-1392. DOI: 10.11852/zgetbjzz2020-0284
临床研究与分析

中性粒细胞明胶酶相关脂质运载蛋白、白细胞介素33、肿瘤坏死   因子α对非常早产儿支气管肺发育不良的早期预测作用

  • 邹巧巧, 王慧琴
作者信息 +

Role of neutrophils gelatinase-associated lipid delivery protein, interleukin-33 and tumor necrosis factor-α in the early prediction of bronchopulmonary dysplasia in very premature infants

  • ZOU Qiao-qiao, WANG Hui-qin
Author information +
文章历史 +

摘要

目的 研究血清中性粒细胞明胶酶相关质运载蛋白(NGAL)、白介素33(IL-33)、肿瘤坏死因子α(TNF-α)对非常早产儿支气管肺发育不良(BPD)的早期预测作用。方法 选取安徽医科大学附属妇幼保健院2018年3月-2019年9月收治的非常早产儿,根据诊断标准分为BPD组和非BPD组。分别检测生后第1、14、28天血清IL-33、TNF-α和NGAL的水平,进行比较分析;并制作受试者工作特征曲线(ROC),判断各个指标早期预测效能。结果 1)共纳入非常早产儿66例,BPD组25例,发生率37.9%,其中轻度15例,中度8例,重度2例;2)不同时间段BPD组血清IL-33、TNF-α和NGAL水平均明显高于非BPD组,差异均有统计学意义(P<0.05),且三者在出生后14 d内的表达水平逐渐升高(P<0.05);3)重度BPD组患儿在第14、28天血清IL-33的表达水平明显高于轻、中度BPD患儿,差异有统计学意义(F=8.220、15.763,P<0.05); 4)ROC 曲线显示NGAL(第1天)、IL-33(第1天)、TNF-α(第1天)、NGAL(第14天)、IL-33(第14天)、TNF-α(第14天)AUC值分别为 0.768、0.752、0.760、0.875、0.978、0.975。结论 IL-33、NGAL、TNF-α均可早期预测BPD的发生,且在生后第1天NGAL早期预测效能最高,第14天IL-33预测效能最高,IL-33还可能是作为评估BPD严重程度的一项指标。

Abstract

Objective To explore the role of serum neutrophil gelatinase-associated carrier protein(NGAL), interleukin 33(IL-33), and tumor necrosis factor alpha(TNF-α) in the early prediction of bronchopulmonary dysplasia(BPD) in very preterm infants. Methods The very premature infants admitted in Maternal and Child Health Hospital of Anhui Medical University from March 2018 to September 2019 were enrolled in this study and were divided into BPD group and non-BPD group according to the diagnostic criteria.The serum levels of IL-33, TNF-α and NGAL on the 1st, 14th and 28th day after birth were tested for comparative analysis, and receiver operating characteristic(ROC) curves were prepared to obtain early predictive efficacy of various indicators. Results 1) A total of 66 very premature infants were included, of whom 25 cases(37.9%) were in the BPD group, including 15 cases of mild BPD, 8 cases of moderate BPD, and 2 cases of severe BPD.2) The serum levels of IL-33, TNF-α and NGAL in the BPD group at different time periods were significantly higher than those in the non-BPD group(P<0.05), and the expression levels of the three indicators gradually increased during 14 days after birth(P<0.05).3) Children in severe BPD group had significantly higher levels of serum IL-33 on the 14th days and 28th days after birth than those with mild to moderate BPD(F=8.220, 15.763, P<0.05).4) ROC curve showed that the areas under curve(AUC) of serum levels of NGAL, IL-33, TNF-α on the 1st and 14th day after birth were 0.768, 0.752, 0.760, 0.875, 0.978 and 0.975, respectively. Conclusions IL-33, NGAL, and TNF-α are all early predictors of BPD, with the highest prediction efficiency of NGAL level on the 1st day after birth, and highest prediction efficiency of IL-33 level on the 14th day.Moreover, IL-33 may also be used as an indicator to assess the severity of BPD.

关键词

支气管肺发育不良 / 早期预测 / 非常早产儿

Key words

bronchopulmonary dysplasia / early prediction / very premature

引用本文

导出引用
邹巧巧, 王慧琴. 中性粒细胞明胶酶相关脂质运载蛋白、白细胞介素33、肿瘤坏死   因子α对非常早产儿支气管肺发育不良的早期预测作用[J]. 中国儿童保健杂志. 2020, 28(12): 1389-1392 https://doi.org/10.11852/zgetbjzz2020-0284
ZOU Qiao-qiao, WANG Hui-qin. Role of neutrophils gelatinase-associated lipid delivery protein, interleukin-33 and tumor necrosis factor-α in the early prediction of bronchopulmonary dysplasia in very premature infants[J]. Chinese Journal of Child Health Care. 2020, 28(12): 1389-1392 https://doi.org/10.11852/zgetbjzz2020-0284
中图分类号: R722.6   

参考文献

[1] 王卫平, 孙锟, 常立文.儿科学[M].9版.北京: 人民卫生出版社,2018:86.
[2] Fonseca LT, Senna DC, Silveira RC, et al.Associationbetweenbreast milk and bronchopulmonary dysplasia: a single center observational study[J].Am J Perinatol, 2017, 34(3):264-269.
[3] Mowitz ME, Ayyagari R, Gao W, et al.Health care burden of bronchopulmonary dysplasia among extremely preterm infants[J].Front Pediatr, 2019, 7(12):510.
[4] Lapcharoensap W, Bennett MV, Xu X, et al.Hospitalization costs associated with bronchopulmonary dysplasia in the first year of life[J].J Perinatol, 2020, 40(1):130-137.
[5] 吴汉项.血脂质运载蛋白、CysC检测在急性肾损伤患者早期诊断的应用[J].中国医学工程, 2019, 27(11):24-27.
[6] 宋醒良, 程艳梅, 黄俊,等.中性粒细胞明胶酶相关脂质运载蛋白在心肾综合征中的早期诊断价值[J].中国当代医药, 2019, 26(27):143-146.
[7] 陈红, 郭晓理.尿KIM-1和NGAL对新生儿窒息肾损伤的诊断研究[J].南通大学学报:医学版, 2019, 39(4):302-304.
[8] Jung M,Mertens C, Bauer R, et al.Lipocalin-2 and iron trafficking in the tumor microenvironment[J].Pharmacol Res, 2017, 120:146-156.
[9] 贺晓雯, 徐玉祥, 张九芝,等.血sCD14-ST联合尿NGAL对早期诊断脓毒血症并发AKI患者的临床价值[J].河北医学, 2019, 25(11):1765-1769.
[10] Inoue H,Ohga S, Kusuda T, et al.Serum neutrophil gelatinase-associated lipocalin as a predictor of the development of bronchopulmonary dysplasia in preterm infants[J].Early Hum Dev, 2013, 89(6):425-429.
[11] Page-McCaw A,Ewald AJ, Werb Z.Matrix metalloproteinases and the regulation of tissue remodelling[J].Nat Rev Mol Cell Biol,2007,8(3):221-233.
[12] Capoluongo E, Vento G, Lulli P, et al.Epithelial lining fluid neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus[J].Int J Im-munopathol Pharmacol, 2008, 21(1):173-179.
[13] Byers DE, Alexander-Brett J, Patel AC, et al.Long-term IL-33-producing epithelial progenitor cells in chronic obstructive lung disease[J].J Clin Invest, 2013, 123(9):3967-3982.
[14] Kamekura R, Kojima T, Takano K, et al.The role of IL-33 and its receptor ST2 in human nasal epithelium with allergic rhinitis[J].Clin Exp Allergy, 2012, 42(2):218-228.
[15] Tang XQ.Interleukin-33(IL-33) increaseshyperoxia-induced bronchopulmonary dysplasia in newborn mice by regulation of inflammatory mediators[J].Med Sci Monit,2018,24: 6717-6728.
[16] Drake LY,Squillace D, Iijlma K, et al.Early life represents a vulnerable time window for IL-33-induced peripheral lung pathology[J].J Immunol, 2019, 203(7):1952-1960.
[17] Cakir U, Tayman C.A novel diagnostic marker for the severity of bronchopulmonary dysplasia in very low birth weight infants: interleukin-33[J].Pediatr Allergy Immunol Pulmonol, 2019, 32(1):12-17.
[18] 屈文静.TNF-α在支气管肺发育不良患儿血浆中的水平及临床意义[J].中国妇幼保健, 2016, 31(1):104-105.
[19] 任平香, 王献华, 蒋建妹, 等.肿瘤坏死因子-α与肺纤维化[J].中国煤炭工业医学杂志, 2007, 10(3):242-244.
[20] 莫炜明, 姚臻, 赵善和,等.早产儿应用rhEPO治疗支气管肺发育不良前后血液中IL-1β、TNF-α变化及意义[J].当代医学, 2015, 21(2):18-19.
[21] 王刚.支气管肺发育不良早产儿血清IL-8和TNF-α水平变化的临床意义[J].中国妇幼保健, 2017, 32(6):1210-1212.

基金

安徽医科大学校科研基金项目(2019xkj171)

PDF(500 KB)

Accesses

Citation

Detail

段落导航
相关文章

/