期刊文献+

MMP-26在IPF中的水平及临床意义

MMP-26 levels in Idiopathic Pulmonary Fibrosis and clinical significance
下载PDF
导出
摘要 目的研究血清MMP-26在IPF患者中的水平,探讨其在IPF患者发病过程中的临床价值。方法收集10例IPF患者血清为实验组、10例健康成人血清为对照组。采用酶联免疫吸附法(ELISA)测定血清MMP-26含量,并与HRCT、动脉血气分析、呼吸困难程度及肺功能进行相关分析。结果健康成人血清MMP-26浓度为(7.33±1.65)μg/L,IPF患者血清MMP-26浓度为(5.72±0.55)μg/L,两者差异有统计学意义(P<0.05)。IPF患者血清MMP-26浓度与HRCT严重程度及呼吸困难严重程度呈负相关,与PaO_2呈正相关,而与P(A-a)O_2、PaCO_2、HCO_3^-浓度水平以及肺功能无明显相关性(P>0.05)。结论 MMP-26可能参与了IPF的发病过程;MMP-26可作为IPF严重程度及预后的一项参考指标。 Objective To study serum MMP-26 levels in patients with idiopathic pulmonary fibrosis( IPF) and explore its clinical significance. Methods Collect 10 patients with IPF as the experimental group,and 10 healthy adults as control group. Using enzyme-linked immunosorbent assay( ELISA) to determine the level of MMP-26 in serum,and analyze the results of high-resolution CT,arterial blood gas analysis,the degree of dyspnea and pulmonary function. Results The MMP-26 concentration( 5. 72 ± 0. 55 μg / l) from patients with IPF was lower than that of normal control group( 7. 33 ± 1. 65 μg / l),and the difference was statistically significant( P〈0. 05). The serum concentration of MMP-26 of the patients with IPF was negatively correlated to the HRCT severity and the severity of dyspnea,while positively correlated to the PaO_2,and the correlations between serum concentration of MMP-26 of the patients with IPF and P( A-a)O_2,PaCO_2,HCO_3^-concentration levels and pulmonary function were not significant. Conclusion MMP-26 may be involved in the pathogenesis of IPF.MMP-26 could be used as a reference index of IPF severity and prognosis.
作者 罗曦 赵勇
出处 《遵义医学院学报》 2016年第1期47-50,共4页 Journal of Zunyi Medical University
基金 遵义汇川区科技局资助项目(NO:209.001.122.09)
关键词 IPF MMP-26 呼吸困难 HRCT 动脉血气分析 IPF MMP-26 dyspnea HRCT arterial blood gas analysis
  • 相关文献

参考文献15

  • 1Olson A L, Swigris J J, Lezotte D C,et al. Mortality frompulmonary fibrosis increased in the United states from1992 to 2003[J]. Am J Respir Crit Care Med,2007,176(3):277 -284. 被引量:1
  • 2Battista G,Zompatori M,Fasano L,et al. Progressive wors-ening of idiopathic pulmonary fibrosis. High resolutioncomputed tomography ( HRCT ) study with functional cor-relations [ J ]. Radiol Med,2003,105(1 -2) :2-11. 被引量:1
  • 3Manali E D, Stathopoulos G T,Kollintza A,et al. TheMedical Research council chronic dyspnea score predictsthe survival of patients with idiopathic pulmonary fibrosis[J]. J Respir Med,2008,102(4) :586 -592. 被引量:1
  • 4Raghu G, Collard H R, Egan J J, et al. An official ATS/ERS/JRS/ALAT statement : idiopathic pulmonary fibosis :evidence - based guidelines for diagnosis and management[J]. Am J Respir Crit Care Med,2011,183 (6) :788 -824. 被引量:1
  • 5向敏,赵勇,王先梅.MMP-7在IPF中的水平及意义[J].遵义医学院学报,2012,35(5):400-403. 被引量:5
  • 6李振华,彭守春,康健,侯显明,于润江.特发性肺纤维化患者死亡预后因素的回顾性队列研究[J].中华结核和呼吸杂志,2010,33(12):887-891. 被引量:13
  • 7Selman M,Ruiz V,Cabrera S,et al. TIMP 一 1,- 2 , 一 3 ,and -4 in idiopathic pulmonary fibrosis. A prevailing non-degradative lung microenvironment ? [ J ]. Am J PhysiolLung Cell Mol Physiol,2000,279(3) :562 -574. 被引量:1
  • 8Marchenko G N, Ratnikov B I, Rozanov D V,et al. Char-acterization of matrix metalloproteinase -26, a novel met-alloproteinase widely expressed in cancer cells of epithelialorigin[ J]. J Biol Chem,2001,356 (Pt 3) :705 -718. 被引量:1
  • 9Uria J A, Lopez - Otin C. Matrilysin - 2, a new matrixmetalloproteinase expressed in human tumors and showingthe minimal domain organization required for secretion,latency,and activity [ J ]. Cancer Res, 2000,60(17):4745 -4751. 被引量:1
  • 10ZhaoY G,Xiao A Z,Park H I,et al. Endometase/mat-rilysin -2 in human breast ductal carcinoma in situ andits inhibition by tissue inhibitors of metalloproteinases - 2and - 4: a putative role in the initiation of breast cancerinvasion[ J]. Cancer Res, 2004,64(2) : 590 -598. 被引量:1

二级参考文献48

  • 1李振华.支气管肺泡灌洗液检查//侯显明,于润江.间质性肺病学.北京:人民卫生出版社,2003:196-197. 被引量:3
  • 2Olson AL,Swigris J J,Lezotte DC,et al.Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003.Am J Respir Crit Care Med,2007,176:277-284. 被引量:1
  • 3American Thoracic Society.Idiopathic pulmonary fibrosis:diagnosis and treatment.International consensus statement.American Thoracic Society (ATS),and the European Respiratory Society (ERS).Am J Respir Crit Care Med,2000,161 (2 Pt 1):646-664. 被引量:1
  • 4Jeon K,Chung MP,Lee KS,et al.Prognostic factors and causes of death in Korean patients with idiopathic pulmonary fibrosis.Respir Med,2006,100:451-457. 被引量:1
  • 5中华医学会呼吸病学分会.支气骨肺泡灌洗液细胞学检测技术规范(草案)[J].中华结核和呼吸杂志,2002,:25-391,390. 被引量:1
  • 6Nathan SD.Lung transplantation:disease-specific considerations for referral.Chest,2005,127:1006-1016. 被引量:1
  • 7Lynch DA,Godwin JD,Safrin S,et al.High-resolution computed tomography in idiopathic pulmonary fibrosis:diagnosis and prognosis.Am J Respir Crit Care Med,2005,172:488-493. 被引量:1
  • 8Collard HR,King TE Jr.Demystifying idiopathic interstitial pneumonia.Arch Intern Med,2003,163:17-29. 被引量:1
  • 9Lama VN,Flaherty KR,Toews GB,et al.Prognostic value of desaturation during a 6-minute walk test in idiopathic interstitial pneumonia.Am J Respir Crit Care Med,2003,168:1084-1090. 被引量:1
  • 10Antoniou KM,Hansell DM,Rubens MB,et al.Idiopathic pulmonary fibrosis:outcome in relation to smoking status.Am J Respir Crit Care Med,2008,177:190-194. 被引量:1

共引文献94

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部