摘要
目的:探讨CD34、Ⅰ型胶原(collagenⅠ,COLⅠ)、CXCR4在支气管肺发育不良(bronchopulmonary dysplasia,BPD)的表达及临床意义。方法:利用流式细胞仪(flow cytometry,FCM)检测61例早产儿生后1、3、5、7、28 d外周血中CD34、COLⅠ、CXCR4的表达,并比较CD34、COLⅠ、CXCR4在BPD组及非BPD组间表达的差异。结果:BPD组患儿较非BPD组患儿CXCR4在生后第1天有明显增高[(61.4±13.37)%]。随着日龄的增大,BPD患儿COLⅠ水平在第28天达到高峰[3.42(2.87,4.98)%],而CD34、CXCR4水平降至最低[(0.67±0.25)%;(31.9±13.48)%]。重复测量设计方差分析显示,日龄的增大及CD34、COLⅠ、CXCR4水平的变化对BPD的发生存在交互作用(F=77.66,P=0.000)。ROC曲线分析显示,COLⅠ的曲线下面积(area under the curve,AUC)为0.867,高于CD34、CXCR4,且当COLⅠ值为1.3%时,敏感度为69.7%,特异度为86%。不同时间点BPD各组测量值比较均有统计学意义(P=0.000)。结论:循环纤维细胞的COLⅠ水平高表达及CD34、CXCR4水平持续降低与BPD的发生密切相关。
Objective:To investigate the expression and clinical significance of CD34,COLⅠ and CXCR4 in bronchopulmonary dysplasia(BPD). Methods:Expressions of CD34,COLⅠ and CXCR4 in peripheral blood from 44 premature infants with BPD on the 1st,3rd,5th,7th and 28 th d after birth were measured by flow cytometry(FCM)and the expression differences of CD34,COL I,CXCR4 between BPD group and the non- BPD group were compared. Results:On the 1st d after birth,the expression of CXCR4 increased greatly in BPD group compared with that of non-BPD group. With the increase of days after birth,COLⅠ level peaked on 28 th d in BPD group,while CD34 and CXCR4 levels reduced to the lowest. Data of ANOVA for repeated measurement showed that time and the changes in CD34,COL I and CXCR4 levels caused an interactive effect on the occurrence of BPD(F=77.66,P=0.000). ROC curve displayed that area under the curve of COL I was 0.867,higher than those of CD34 and CXCR4. When COL I was 1.3%,the sensitivity was 69.7% and specificity was 86%. There were statistically significances in BPD group among different time points(P =0.000).Conclusion:Circulating fibrocytes with increased level of COLⅠ as well as decreased level of CD34 and CXCR4 are closely related with the occurrence of BPD.
出处
《重庆医科大学学报》
CAS
CSCD
北大核心
2015年第4期627-631,共5页
Journal of Chongqing Medical University
基金
重庆市卫生局医学科学技术研究资助项目(编号:2008-2-159)
“国家临床重点专科-新生儿学”资助项目(编号:卫办医政函【2011】873号)
关键词
早产儿
循环纤维细胞
支气管肺发育不良
premature infants
circulating fibrocytes
bronchopulmonary dysplasia