Role of endothelial damage in the pathogenesis of interstitial pneumonitis in patients with polymyositis and dermatomyositis

J Rheumatol. 2006 May;33(5):903-6.

Abstract

Objective: Polymyositis and dermatomyositis (PM/DM) are often complicated by interstitial pneumonitis (IP), which is an important cause of death. It has been reported that blood concentration of transforming growth factor-beta (TGF-beta), which is produced by a wide range of cells including endothelial cells and enhances the fibrotic changes in various tissues, is increased in PM/DM with IP. Endothelial damage is likely to exist in PM/DM. We studied the relationship between endothelial damage and IP in PM/DM.

Methods: Blood levels of sialylated carbohydrate antigen KL-6, TGF-beta, endothelin-1 (ET-1), thrombomodulin (TM), and plasminogen activator inhibitor-1 (PAI-1) were determined in 43 patients with PM or DM with or without IP, and the relationship between these measures was analyzed.

Results: Blood levels of KL-6 and TGF-beta were higher in the patients with IP than those without, and these measures were well correlated with each other. Levels of ET-1, TM, and PAI-1, all known to reflect the extent of endothelial damage, were also increased in patients with IP, and these measures correlated well with TGF-beta.

Conclusion: Our data suggest that endothelial damage might play an important role through the production of fibrosis-enhancing factors such as TGF-beta or ET-1 in PM/DM.

MeSH terms

  • Adult
  • Aged
  • Antigens, Neoplasm / blood
  • Antigens, Neoplasm / physiology
  • Blood Cell Count
  • Dermatomyositis / blood
  • Dermatomyositis / complications*
  • Dermatomyositis / physiopathology
  • Endothelin-1 / blood
  • Endothelin-1 / physiology
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / physiopathology*
  • Humans
  • Lung Diseases, Interstitial / blood
  • Lung Diseases, Interstitial / etiology*
  • Lung Diseases, Interstitial / physiopathology
  • Middle Aged
  • Mucin-1
  • Mucins / blood
  • Mucins / physiology
  • Plasminogen Activator Inhibitor 1 / blood
  • Plasminogen Activator Inhibitor 1 / physiology
  • Polymyositis / blood
  • Polymyositis / complications*
  • Polymyositis / physiopathology
  • Thrombomodulin / blood
  • Thrombomodulin / physiology
  • Transforming Growth Factor beta / blood
  • Transforming Growth Factor beta / physiology

Substances

  • Antigens, Neoplasm
  • Endothelin-1
  • MUC1 protein, human
  • Mucin-1
  • Mucins
  • Plasminogen Activator Inhibitor 1
  • Thrombomodulin
  • Transforming Growth Factor beta