Baseline Platelet Activation and Reactivity in Patients with Critical Limb Ischemia

PLoS One. 2015 Jul 6;10(7):e0131356. doi: 10.1371/journal.pone.0131356. eCollection 2015.

Abstract

Background: Patients with critical limb ischemia (CLI) have a high risk to develop cardiovascular events (CVE). We hypothesized that in CLI patients platelets would display increased baseline activation and reactivity.

Objectives: We investigated baseline platelet activation and platelet reactivity in patients with CLI.

Patients/methods: In this study baseline platelet activation and platelet reactivity in response to stimulation of all major platelet activation pathways were determined in 20 CLI patients (11 using aspirin and 9 using vitamin K-antagonists) included in the Juventas-trial (clinicaltrials.gov NCT00371371) and in 17 healthy controls. Platelet activation was quantified with flow cytometric measurement of platelet P-selectin expression and fibrinogen binding.

Results: CLI patients not using aspirin showed higher baseline platelet activation compared to healthy controls. Maximal reactivity to stimulation of the collagen and thrombin activation pathway was decreased in CLI patients compared to healthy controls. In line, attenuated platelet reactivity to stimulation of multiple activation pathways was associated with several traditional risk factors for cardiovascular disease.

Conclusions: Baseline platelet activation was increased in CLI patients, whereas the reactivity of circulating platelets to several stimulatory agents is decreased. Reactivity of platelets was inversely correlated with cardiovascular risk factors.

Publication types

  • Clinical Trial

MeSH terms

  • Aspirin / therapeutic use
  • Blood Platelets / drug effects
  • Blood Platelets / metabolism
  • Blood Platelets / pathology*
  • Cardiovascular Diseases / metabolism
  • Cardiovascular Diseases / physiopathology
  • Case-Control Studies
  • Collagen / metabolism
  • Female
  • Fibrinogen / metabolism
  • Humans
  • Ischemia / drug therapy
  • Ischemia / metabolism
  • Ischemia / pathology*
  • Male
  • Middle Aged
  • Peripheral Arterial Disease / drug therapy
  • Peripheral Arterial Disease / metabolism
  • Peripheral Arterial Disease / pathology*
  • Platelet Activation / drug effects
  • Platelet Activation / physiology*
  • Risk Factors
  • Thrombin / metabolism

Substances

  • Fibrinogen
  • Collagen
  • Thrombin
  • Aspirin

Associated data

  • ClinicalTrials.gov/NCT00371371

Grants and funding

The authors have no support or funding to report.