The Link between Arterial Atherosclerotic Disease and Venous Thromboembolic Disease

Pavel Poredos1,2, Peter Poredos2,3, Mateja K Jezovnik4

  • 1Department of Vascular Disease, University Medical Center Ljubljana, Slovenia.

PubMed

Insights

Arterial atherosclerotic and venous thromboembolic diseases share common risk factors and similar inflammatory mechanisms. This suggests a unified approach to prevention and treatment could improve outcomes for both vascular conditions.

Area of Science:

  • Cardiovascular Medicine
  • Vascular Biology
  • Thrombosis Research

Background:

  • Arterial atherosclerotic (AA) and venous thromboembolic (VTE) diseases are traditionally viewed as distinct entities.
  • Emerging evidence highlights significant links and shared characteristics between AA and VTE.
  • Understanding these connections is crucial for comprehensive vascular disease management.

Purpose of the Study:

  • To review the relationship between arterial and venous vascular diseases.
  • To explore common risk factors and etiological mechanisms.
  • To discuss the implications for unified prevention and treatment strategies.

Main Methods:

  • Narrative review of existing literature.
  • Analysis of shared risk factors (dyslipidemia, metabolic syndrome, thrombophilia).
  • Examination of common pathogenetic mechanisms, particularly inflammation.

Main Results:

  • Shared risk factors like dyslipidemia and metabolic syndrome are prevalent in both AA and VTE.
  • Inflammation plays a key role in the pathogenesis of both conditions, promoting coagulation.
  • Evidence links preclinical/clinical atherosclerosis with VTE, suggesting atherosclerosis may induce VTE or share common drivers.
  • Pharmacological interventions like antiplatelets, anticoagulants, and statins show efficacy in preventing both AA and VTE.

Conclusions:

  • Arterial and venous diseases share fundamental pathophysiological mechanisms and common risk factors.
  • A unified approach to the prevention and treatment of these vascular conditions is warranted.
  • Addressing shared pathways may lead to improved patient outcomes in both arterial and venous diseases.

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