>
网站首页期刊介绍通知公告编 委 会投稿须知电子期刊广告合作联系我们
最新消息:
肺炎支原体肺炎患儿外周血miR-106a、miR-20a表达与胸部X线表现及炎症的相关性
作者:赵肖依  耿思思  张雅尚  吕晓倩 
单位:衡水市人民医院小儿内科, 河北 衡水 053000
关键词:miR-106a miR-20a 肺炎支原体肺炎 胸部X线 炎症 
分类号:R725.6
出版年·卷·期(页码):2024·43·第一期(25-33)
摘要:

目的: 探讨肺炎支原体肺炎(MPP)患儿外周血微小RNA(miR)-106a、miR-20a表达与胸部X线(CXR)表现及炎症的相关性。方法: 选取2020年1月至2021年12月本院收治的393例MPP患儿作为研究对象。采用全自动血细胞分析仪检测白细胞计数、红细胞计数、血小板计数、中性分叶核白细胞等,免疫透射比浊法检测C反应蛋白(CRP)水平。采用实时定量聚合酶链反应法检测外周血miR-106a和miR-20a表达。所有患儿均在入组后接受CXR检查。结果: MPP患儿外周血miR-106a和miR-20a的表达水平分别为1.00(0.61,2.11)、1.06(0.73,1.67)。根据中位值分组,与miR-106a和miR-20a低表达组相比,高表达组患儿CRP水平和肺实变患儿比例明显更高(P<0.05);miR-20a高表达组患儿胸腔积液患儿比例也显著高于低表达组(P<0.05)。MPP患儿外周血miR-106a和miR-20a与CRP呈显著正相关(r值分别为0.212、0.230,均P<0.001)。肺实变组外周血miR-106a和miR-20a表达水平均显著高于非肺实变组(P<0.05)。经ROC曲线分析,外周血miR-106a和miR-20a预测MPP肺实变的曲线下面积(AUC)为0.811(95%CI: 0.767~0.855)、0.807(95%CI: 0.762~0.852),灵敏度分别为75.3%和77.4%,特异度分别为76.5%和76.4%,对应的截断值为1.20和1.18。Logistic回归分析显示,外周血miR-106a和miR-20a高表达是MPP肺实变的独立影响因素(P<0.05)。结论: MPP患儿外周血miR-106a和miR-20a过表达与CXR严重表现和炎症加重有关,两者可作为指示MPP严重程度和炎症进展的标志物。

Objective: To investigate the correlation between peripheral blood microrna(miR)-106a and miR-20a expression and chest X-ray(CXR) manifestations and inflammation in children with Mycoplasma pneumoniae pneumonia(MPP). Methods: 393 children with MPP admitted to our hospital from January 2020 to December 2021 were selected as research objects. White blood cell count,red blood cell count,platelet count and neutral lobed nucleus leukocyte were measured by automatic blood cell analyzer,and C-reactive protein(CRP) was detected by immunoturbidimetry. The expression of miR-106a and miR-20a in peripheral blood was detected by real-time quantitative polymerase chain reaction. All patients underwent CXR examination after enrollment. Results: The expression levels of miR-106a and miR-20a in peripheral blood of MPP patients were 1.00(0.61,2.11) and 1.06(0.73,1.67),respectively. After grouping based on median values,compared with miR-106a and miR-20a low expression groups,the level of CRP and the proportion of lung consolidation patients in the high expression group were significantly higher(P<0.05). Moreover,the proportion of children with pleural effusion in the high expression group of miR-20a was significantly higher than that in the low expression group(P<0.05). There was a significant positive correlation between peripheral blood miR-106a and miR-20a in MPP patients and CRP(r=0.212,0.230,P<0.001). The expression levels of miR-106a and miR-20a in peripheral blood of the lung consolidation group were significantly higher than those of the non lung consolidation group(P<0.05). According to ROC curve analysis,the area under the curve(AUC) of peripheral blood miR-106a and miR-20a for predicting MPP lung consolidation were 0.811(95%CI:0.767-0.855) and 0.807(95%CI:0.762-0.852),with a sensitivity of 75.3% and 77.4%,a specificity of 76.5% and 76.4%,and corresponding cutoff values of 1.20 and 1.18,respectively. Logistic regression analysis showed that high expression of miR-106a and miR-20a in peripheral blood was an independent influencing factor for MPP pulmonary consolidation(P<0.05).Conclusion: The overexpression of miR-106a and miR-20a in peripheral blood of children with MPP is associated with severe CXR manifestations and increased inflammation,which may be used as markers to indicate the severity of MPP and the progression of inflammation.

参考文献:

[1] 杨旭,李颖,马艳玲.血清miR-195-5p、IL-17对小儿支原体肺炎早期诊断价值的研究[J].现代医学,2022,50(7):875-879.
[2] 李琳楠,王永芳,程艳波,等.血清中IL-17、NF-κB表达水平对儿童肺炎支原体肺炎肺实变的早期诊断作用[J].新医学,2023,54(5):350-353.
[3] JIA Z,SUN Q,ZHENG Y,et al.The immunogenic involvement of miRNA-492 in mycoplasma pneumoniae infection in pediatric patients[J].J Pediatr(Rio J),2023,99(2):187-192.
[4] YIN L,MA Y,WANG W,et al.The critical function of miR-1323/Il6 axis in children with Mycoplasma pneumoniae pneumonia[J].J Pediatr(Rio J),2021,97(5):552-558.
[5] DONDE M J,ROCHUSSEN A M,KAPOOR S,et al.Targeting non-coding RNA family members with artificial endonuclease XNAzymes[J].Commun Biol,2022,5(1):1010-1019.
[6] 李丽,张静,郭锦涛.微小RNA-106 a靶向PTEN通路对胃癌细胞的增殖与凋亡的调控作用[J].实用癌症杂志,2021,36(1):20-23,27.
[7] AHMED MOHMMED E,SHOUSHA W G,EL-SAIID A S,et al.A clinical evaluation of circulating miR-106a and Raf-1 as breast cancer diagnostic and prognostic markers[J].Asian Pac J Cancer Prev,2021,22(11):3513-3520.
[8] SANCTUARY M R,HUANG R H,JONES A A,et al.miR-106a deficiency attenuates inflammation in murine IBD models[J].Mucosal Immunol,2019,12(1):200-211.
[9] ZHU D,PAN C,LI L,et al.MicroRNA-17/20a/106a modulate macrophage inflammatory responses through targeting signal-regulatory protein ɑ[J].J Allergy Clin Immunol,2013,132(2):426-436.e8.
[10] ZHAO H,GONG N.miR-20a regulates inflammatory in osteoarthritis by targeting the IκBβ and regulates NK-κB signaling pathway activation[J].Biochem Biophys Res Commun,2019,518(4):632-637.
[11] BAI Y,LI H,DONG J.Up-regulation of miR-20a weakens inflammation and apoptosis in high-glucose-induced renal tubular cell mediating diabetic kidney disease by repressing CXCL8 expression[J].Arch Physiol Biochem,2022,128(6):1603-1610.
[12] 胡正权,孙欣娜,杨青.microRNA 20a通过核因子-κB信号通路影响肺炎模型幼鼠炎症水平的机制研究[J].临床和实验医学杂志,2020,19(8):815-819.
[13] 中华人民共和国国家卫生健康委员会.儿童肺炎支原体肺炎诊疗指南(2023年版)[J].国际流行病学传染病学杂志,2023,50(2):79-85.
[14] MOHAMED H A,ABDELKAFY A E,KHAIRY R M M,et al.MicroRNAs and cytokines as potential predictive biomarkers for COVID-19 disease progression[J].Sci Rep,2023,13(1):3531-3541.
[15] SHEN Y,YU J,JING Y,et al.MiR-106a aggravates sepsis-induced acute kidney injury by targeting THBS2 in mice model[J].Acta Cir Bras,2019,34(6):e201900602.
[16] FUENTES N,ROY A,MISHRA V,et al.Sex-specific microRNA expression networks in an acute mouse model of ozone-induced lung inflammation[J].Biol Sex Differ,2018,9(1):18-30.
[17] 刘会永,李彦,黄燕.溃疡性结肠炎患者血浆miR-106a和miR-363-3p表达水平的变化及意义[J].国际消化病杂志,2019,39(5):341-346.
[18] HENG J,WU D,LU S,et al.miR-106a targets anoctamin 1(ANO1) to regulate lipopolysaccharide(LPS)-induced inflammatory response in macrophages[J].Med Sci Monit,2020,26:e922479.
[19] YANG J,CHEN Y,JIANG K,et al.MicroRNA-106a provides negative feedback regulation in lipopolysaccharide-induced inflammation by targeting TLR4[J].Int J Biol Sci,2019,15(11):2308-2319.
[20] 刘春艳,柯文玲,柴林,等.血清中microRNA 20a与小儿肺炎炎症反应进展的相关性研究[J].中国儿童保健杂志,2019,27(8):881-884.
[21] LIU Z,YU H,GUO Q.MicroRNA-20a promotes inflammation via the nuclear factor-κB signaling pathway in pediatric pneumonia[J].Mol Med Rep,2018,17(1):612-617.
[22] GONG Y,XU W,CHEN Y,et al.miR-20a-5p regulates pulmonary surfactant gene expression in alveolar type II cells[J].J Cell Mol Med,2019,23(11):7664-7672.

服务与反馈:
文章下载】【发表评论】【查看评论】【加入收藏
提示:您还未登录,请登录!点此登录
您是第 413084 位访问者


copyright ©《东南大学学报(医学版)》编辑部
联系电话:025-83272481 83272483
电子邮件:
bjb@pub.seu.edu.cn

苏ICP备09058364