Pathogenesis of cardiovascular events in BCR-ABL1-negative myeloproliferative neoplasms

Leukemia. 2021 Apr;35(4):935-955. doi: 10.1038/s41375-021-01170-z. Epub 2021 Mar 3.

Abstract

Thrombosis, both in arterial and venous territories, is the major complication of myeloproliferative neoplasms and is responsible for a high rate of morbidity and mortality. The currently accepted risk factors are an age over 60 years and a history of thrombosis. However, many complex mechanisms contribute to this increased prothrombotic risk, with involvement of all blood cell types, plasmatic factors, and endothelial cells. Besides, some cardiovascular events may originate from arterial vasospasm that could contribute to thrombotic complications. In this review, we discuss recent results obtained in mouse models in the light of data obtained from clinical studies. We emphasize on actors of thrombosis that are currently not targeted with current therapeutics but could be promising targets, i.e, neutrophil extracellular traps and vascular reactivity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Blood Cells / immunology
  • Blood Cells / metabolism
  • Blood Coagulation
  • Blood Coagulation Factors / metabolism
  • Blood Vessels / metabolism
  • Cardiovascular Diseases / diagnosis
  • Cardiovascular Diseases / epidemiology
  • Cardiovascular Diseases / etiology*
  • Cardiovascular Diseases / therapy
  • Disease Management
  • Disease Models, Animal
  • Disease Susceptibility*
  • Fusion Proteins, bcr-abl / genetics*
  • Hemostasis
  • Humans
  • Mutation
  • Myeloproliferative Disorders / complications*
  • Myeloproliferative Disorders / diagnosis
  • Myeloproliferative Disorders / epidemiology
  • Myeloproliferative Disorders / genetics*
  • Risk Assessment
  • Risk Factors
  • Signal Transduction
  • Thrombosis / blood
  • Thrombosis / diagnosis
  • Thrombosis / etiology

Substances

  • BCR-ABL1 fusion protein, human
  • Biomarkers
  • Blood Coagulation Factors
  • Fusion Proteins, bcr-abl