Impact of markers of endothelial injury and hypercoagulability on systemic lupus erythematosus

Lupus. 2020 Feb;29(2):182-190. doi: 10.1177/0961203319899478. Epub 2020 Jan 16.

Abstract

We have explored the relationship between possible hemostatic changes and clinical manifestation of the systemic lupus erythematosus (SLE) as a function of greater or lesser disease activity according to Systemic Lupus Erythematosus Disease Activity Index-2000 (SLEDAI-2K) criteria. Endothelial injury and hypercoagulability were investigated in patients with SLE by measuring thrombomodulin (TM), D-dimer (DDi) and thrombin generation (TG) potential. A total of 90 participants were distributed into three groups: 1) women with SLE presenting with low disease activity (laSLE) (SLEDAI-2K ≤ 4), 2) women with SLE presenting with moderate to high disease activity (mhaSLE) (SLEDAI-2K > 4), and 3) a control group comprising healthy women. Levels of TM and DDi were higher both in the laSLE and mhaSLE groups compared to controls and in mhaSLE compared to the laSLE group. With respect to TG assay, lagtime and endogen thrombin potential, low concentrations of tissue factor provided the best results for discrimination among groups. Analysis of these data allow us to conclude that TM, DDi and TG are potentially useful markers for discriminating patients with very active from those with lower active disease. Higher SLE activity may cause endothelial injury, resulting in higher TG and consequently a hypercoagulability state underlying the picture of thrombosis common in this inflammatory disease.

Keywords: D-dimer; hypercoagulability; systemic lupus erythematosus; thrombin generation; thrombomodulin.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Case-Control Studies
  • Cross-Sectional Studies
  • Endothelium, Vascular / pathology*
  • Endothelium, Vascular / physiopathology
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis
  • Humans
  • Lupus Erythematosus, Systemic / blood*
  • Lupus Erythematosus, Systemic / pathology*
  • Lupus Erythematosus, Systemic / physiopathology
  • Male
  • Middle Aged
  • Severity of Illness Index
  • Thrombomodulin / blood
  • Thrombophilia / pathology*
  • Thrombophilia / physiopathology
  • Thromboplastin / analysis
  • Young Adult

Substances

  • Biomarkers
  • Fibrin Fibrinogen Degradation Products
  • Thrombomodulin
  • fibrin fragment D
  • Thromboplastin