Elevated plasma levels of soluble platelet glycoprotein VI (GPVI) in patients with thrombotic microangiopathy

Yoshiki Yamashita1, Katsuki Naitoh2, Hideo Wada3

  • 1Departments of Hematology and Oncology, Mie University Hospital and Mie University Graduate School of Medicine, Tsu, Japan.

Thrombosis Research
|December 12, 2013
PubMed
Abstract

Insights

Soluble platelet glycoprotein VI (sGPVI) levels are elevated in thrombotic microangiopathy (TMA) and disseminated intravascular coagulation (DIC). Measuring sGPVI aids in diagnosing and evaluating TMA, especially when ADAMTS13 levels are not markedly reduced.

Area of Science:

  • Hematology
  • Vascular Biology
  • Thrombosis Research

Background:

  • Thrombotic microangiopathy (TMA) encompasses diverse conditions.
  • Pathologies include reduced ADAMTS13 activity, endothelial cell injury, and platelet activation.
  • Platelet activation is a key factor in thrombotic states.

Purpose of the Study:

  • To investigate soluble platelet glycoprotein VI (sGPVI) levels in TMA patients.
  • To assess the role of sGPVI as a marker of platelet activation in thrombosis.

Main Methods:

  • Plasma levels of sGPVI were measured.
  • ADAMTS13 activity, von Willebrand factor (VWF), and VWF propeptide (VWFpp) were also quantified.
  • Patient cohorts included TMA, disseminated intravascular coagulation (DIC), and postoperative groups.

Main Results:

  • Significantly higher sGPVI levels were observed in TMA, DIC, and postoperative patients compared to non-thrombotic controls.
  • Elevated sGPVI was most pronounced in TMA patients with normal or near-normal ADAMTS13 activity.
  • Plasma exchange led to a significant reduction in sGPVI levels in TMA patients.

Conclusions:

  • sGPVI is a sensitive indicator of platelet activation in thrombotic conditions.
  • sGPVI measurement is valuable for diagnosing and monitoring TMA.
  • The marker is particularly useful in TMA cases not primarily driven by severe ADAMTS13 deficiency.

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