A panel of microRNAs as a new biomarkers for the detection of deep vein thrombosis
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  • 作者:Jizheng Qin (1) (2)
    Hongwei Liang (3)
    Dongquan Shi (1) (2)
    Jin Dai (1) (2)
    Zhihong Xu (1) (2)
    Dongyang Chen (1) (2)
    Xi Chen (3)
    Qing Jiang (1) (2)
  • 关键词:Deep vein thrombosis ; MicroRNA ; Biomarker ; Serum
  • 刊名:Journal of Thrombosis and Thrombolysis
  • 出版年:2015
  • 出版时间:February 2015
  • 年:2015
  • 卷:39
  • 期:2
  • 页码:215-221
  • 全文大小:318 KB
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  • 作者单位:Jizheng Qin (1) (2)
    Hongwei Liang (3)
    Dongquan Shi (1) (2)
    Jin Dai (1) (2)
    Zhihong Xu (1) (2)
    Dongyang Chen (1) (2)
    Xi Chen (3)
    Qing Jiang (1) (2)

    1. The Center of Diagnosis and Treatment for Joint Disease, Drum Tower Hospital Affiliated to Medical School of Nanjing University, Zhongshan Road 321, Nanjing, 210008, Jiangsu, People鈥檚 Republic of China
    2. Joint Research Center for Bone and Joint Disease, Model Animal Research Center (MARC), Nanjing University, Nanjing, Jiangsu, People鈥檚 Republic of China
    3. Jiangsu Engineering Research Center for microRNA Biology and Biotechnology, State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, Jiangsu, People鈥檚 Republic of China
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Cardiology
    Hematology
  • 出版者:Springer Netherlands
  • ISSN:1573-742X
文摘
Deep vein thrombosis is one of the common complications of orthopedic surgery, and pulmonary embolism which is one of its lethal complications can lead to mortality. Numerous efforts have been made to identify reliable and predictive biomarkers to detect the early signs of deep vein thrombosis. These studies have, however, not delivered any more informative candidates than the D-dimer that have been available. Cell-free microRNAs are present in a range of body fluids and have recently been shown to be useful biomarkers in many diseases. Therefore, the purpose of present study was to identify potential microRNA biomarkers of deep vein thrombosis that are present in serum. Serum samples were taken from 18 deep vein thrombosis patients and 20 age- and sex-matched controls. TaqMan microRNA array was used for an initial screening. Real-time PCR assay was implemented to confirm the concentrations of candidate microRNAs. We found that the serum levels of miR-582, miR-195 and miR-532 of deep vein thrombosis patients were higher than those of controls. miR-582 yielded an AUC (the areas under the ROC curve) of 0.959, and the other two microRNAs yielded an AUC of 1.000 in discriminating deep vein thrombosis from controls. These data hint that serum miR-582, miR-195 and miR-532 might have potential to be a novel noninvasive biomarkers for detection of DVT. And this is the first study suggesting that serum microNRAs might be used as biomarkers for deep vein thrombosis.

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