临床荟萃

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去泛素化酶Usp46基因在系统性红斑狼疮患者血液中的表达及意义

  

  1. 1.河北医科大学 病理教研室,河北 石家庄 050017;2.河北省人民医院医院 a.感染管理科;b.免疫风湿科,河北 石家庄 050051;
    3.河北医科大学第二医院 免疫风湿科,河北 石家庄 050000
  • 出版日期:2017-08-05 发布日期:2017-08-10
  • 通讯作者: 通信作者:刘淑霞,Email: susanliu1976@163.com
  • 基金资助:
    河北省自然科学基金(H2015206449);河北省卫生厅重点科技研究计划(ZD20140034);河北省大学生创新创业训练计划(201510089038)

Role of  ubiquitinspecific proteases 46  gene in blood of patients with systemic lupus erythematosus

  1. 1.Department of Pathology, Hebei Medical University, Shijiazhuang 050017,China;
    2a.Department of Nosocomial Infection Control;2b.Department of Rheumatology,
    Hebei General Hospital, Shijiazhuang 050051,China; 3.Department of Rheumatology,
    the Second Hospital of Hebei Medical University, Shijiazhuang 050000,China
  • Online:2017-08-05 Published:2017-08-10
  • Contact: Corresponding author: Liu Shuxia,Email: susanliu1976@163.com

摘要: 目的  研究泛素特异性蛋白酶46 (Usp46)基因在系统性红斑狼疮(SLE)患者及健康人外周血中的表达水平,并探讨其在SLE发病中的作用。方法 收集73例SLE患者及75 例健康人临床资料,采用Realtime PCR法检测外周血中Usp46基因 mRNA的表达情况,分析其表达水平与临床指标的关系。结果 与健康对照组相比,SLE患者血液中Usp46基因的mRNA表达水平明显升高(Z=-6.98,P<0.01);在SLE患者中Usp46基因的mRNA表达水平与红细胞沉降率(ESR)、IgG、IgM和谷丙转氨酶(ALT)呈正相关(P<0.05)。结论 Usp46基因的mRNA表达水平在SLE患者血液中明显增高,提示Usp46基因可能参与SLE疾病的发生发展过程。

关键词: 红斑狼疮, 系统性;基因;血沉;泛素特异性蛋白酶46

Abstract: Objective  To investigate the role of  ubiquitinspecific proteases 46 (Usp46) in the blood of systemic lupus erythematosus (SLE) patients and healthy population. Methods  Real  time polymerase chain reaction analysis was used to determine the Usp46 expression in the blood of 73 patients with SLE and 75 healthy controls.Results  The mRNA expression level of Usp46 was significantly increased, about 4.22(1.30,17.02)  folds, in samples from SLE patients compared to healthy population (Z=-6.98,P<0.01). In addition, there was significantly positive correlation between the expression level of Usp46 and ESR, IgG, IgM and ALT (P<0.05). Conclusion  The mRNA expression level of Usp46 was significantly higher in SLE patients than in healthy population, which indicates that Usp46 may participate in the development of SLE process.

Key words: lupus erythematosus, systemic;genes;blood sedimentation;ubiquitin specific protease 46