Journal of Capital Medical University ›› 2018, Vol. 39 ›› Issue (3): 314-319.doi: 10.3969/j.issn.1006-7795.2018.03.002

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Release of cytokines after joint bleeding and the formation of haemophilic arthropathy in children with severe hemophilia A

Liu Guoqing, Chen Zhenping, Tang Ling, Wu Xinyi, Zhen Yingzi, Li Gang, Wang Yan, Zhang Ningning, Zhang Jishui, Yu Guoxia, Wu Runhui   

  1. Hematology Oncology Center, Beijing Children's Hospital, Capital Medical University;Beijing Key Laboratory of Pediatric Hematology Oncology;MOE Key Laboratory of Major Diseases in Children, National Key Discipline of Pediatrics, Ministry of Education, Beijing 100045, China
  • Received:2018-03-08 Online:2018-05-21 Published:2018-06-11
  • Supported by:
    This study was supported by Natural Science Foundation of Beijing (7162059), Capital Health Research and Development of Special (2014-2-2092),Beijing Municipal Administration of Hospital Clinical Medicine Development(ZY201404), the NOVO Nordisk Funding Project.

Abstract: Objective To explore the role of inflammatory factors[interleukin-1β(IL-1β),interleukin-6 (IL-6), tumor necrosis factor-α(TNF-α)] in the formation of haemophilic arthropathy in children with severe hemophilia A, and to provide theoretical basis for further prevention and treatment target of hemophilia joint disease.Methods The eligibility hemophilia A children were enrolled from the Hemophilia Outpatient Clinic of Beijing Children Hospital during 2015-2016. Patients were divided into non-joint bleeding(NJB) group, joint bleeding(JB) group[acute joint bleeding(AJB) group, chronic joint bleeding(CJB) group]. Peripheral venous blood was collected, the expression of IL-1β, IL-6 and TNF-α in blood serum were detected by enzyme-linked immunosorbent assay (enzyme-linked immunosorbent assay, ELISA). The expression of mRNA of IL-1β, IL-6 and TNF-α was detected by reverse transcription-polymerase chain reaction (RT-PCR).Statistical analysis the levels of IL-1β, IL-6 and TNF-α in blood serum and their mRNA expression.Results A total of 47 cases were collected in the patients group, including 17cases of NJB group, 17 cases of AJB group (8 cases with target joint, 9 cases without target joint) and 13 cases of CJB group. Median age was 5.5 years (2 years to18 years). There was significant difference in the expression of mRNA of TNF-α between NJB group, JB group and AJB group(P<0.05). There was significant difference in the expression of mRNA of TNF-α between AJB group with arthropathy (n=8, 5.584±3.634) and AJB group without arthropathy (n=9, 1.680±1.590) (P=0.02).Conclusion The expression of IL-1β, IL-6 and TNF-α in children with hemophilia increased in acute joint bleeding, and the expression of TNF-α increased mainly in acute, chronic and with haemophilic arthropathy, so TNF-α is the key of cytokines in the formation of haemophilic arthropathy in children with severe hemophilia A.

Key words: children with severe hemophilia A, haemophilic arthropathy, inflammatory factors

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