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外周血hsa-miR-342-5p 诊断儿童结核的特异度和灵敏度

  • 周梦瑶 ,
  • 詹学 ,
  • 张祯祯
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  • 重庆医科大学附属儿童医院 儿童发育疾病研究省部共建教育部重点实验室 儿科学重庆市重点实验室 重庆市( 儿童发育重大疾病诊治与预防) 国际科技合作基地( 重庆 400014)

收稿日期: 2015-09-15

  网络出版日期: 2015-09-15

基金资助

国家自然科学基金面上项目 (No.81071406);重庆市医学科研项目计划 (No.20142046)

The sensitivity and specificity analysis of circulating hsa-miR-342-5p to diagnose childhood tuberculosis

  • ZHOU Mengyao ,
  • ZHAN Xue ,
  • ZHANG Zhenzhen
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  • The Children’s Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Chongqing 400014, China

Received date: 2015-09-15

  Online published: 2015-09-15

摘要

目的 评估外周血hsa-miR-342-5p检测对早期诊断儿童结核的价值。方法 收集初治涂片阳性、涂片阴性结核患儿,肺炎患儿和正常儿童各20例,采集静脉血,TRIzol法提取外周血总RNA,qRT-PCR检测hsa-miR-342-5p在各组间的相对表达水平,ROC曲线分析hsa-miR-342-5p诊断儿童结核的特异度和灵敏度。结果 hsa-miR-342-5p在涂片阳性结核、涂片阴性结核患儿、肺炎患儿和正常儿童四组间的差异具有统计学意义(F =21.94,P =0.00)。与正常儿童相比,hsamiR-342-5p在涂片阳性结核、涂片阴性结核和肺炎患儿中的表达水平均下调,差异有统计学意义(P 均<0.01);与肺炎患儿相比,hsa-miR-342-5p在涂片阳性结核、涂片阴性结核患儿中的表达也明显下调,差异有统计学意义(P<0.01)。对于区分涂片阳性结核和肺炎,hsa-miR-342-5p的特异度和灵敏度性均为90%;而区分涂片阴性结核和肺炎,其特异度和灵敏度分别为65%和100%。结论 外周血hsa-miR-342-5p有望成为新的分子指标用于儿童结核的早期诊断。

本文引用格式

周梦瑶 , 詹学 , 张祯祯 . 外周血hsa-miR-342-5p 诊断儿童结核的特异度和灵敏度[J]. 临床儿科杂志, 2015 , 33(9) : 784 . DOI: 10.3969 j.issn.1000-3606.2015.09.006

Abstract

 Objective  To evaluate the value of hsa-miR-342-5p for the childhood tuberculosis (TB) diagnosis. Methods   Twenty culture-positive TB, 20 culture-negative TB, 20 pneumonia and 20 healthy children were enrolled in the study. The venous blood was collected. The peripheral blood total RNA was extracted by TRIzol reagent. The expression of hsa-miR-342- 5p was detected by qRT-PCR. Receiver operating characteristic (ROC) curve was used to evaluate the sensitivity and specificity of hsa-miR-342-5p to diagnose childhood TB. Results There was a significant difference of hsa-miR-342-5p level among culture-positive TB, culture-negative TB, pneumonia and healthy controls (F=21.94, P=0.00). Compared to health control, hsamiR- 342-5p was significantly lower in culture-positive TB, culture-negative TB, and pneumonia children (P<0.01). Compared to pneumonia children, hsa-miR-342-5p was also significantly lower in culture-positive TB and culture-negative TB groups (P<0.01). For distinguish culture-positive TB and pneumonia by hsa-miR-342-5p, the sensitivity and specificity were 90% and 90% respectively. For distinguish culture-negative TB and pneumonia by hsa-miR-342-5p, the sensitivity and specificity were 65% and 100% respectively. Conclusions  The peripheral hsa-miR-342-5p is expected to become a new biomarker for early diagnosis of tuberculosis in children.
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