Impact of LDL-apheresis on inflammation and microcirculation

Atheroscler Suppl. 2009 Dec 29;10(5):56-8. doi: 10.1016/S1567-5688(09)71812-4.

Abstract

Lipid-apheresis (LIPID-A) is highly effective in reduction of pro-atherosclerotic LDL-cholesterol and lipoprotein (a). It has been demonstrated in prospective and retrospective analyses to reduce major cardiovascular events. In addition to improvement of pro-atherosclerotic lipoprotein milieu, LIPID-A exerts pleiotropic effects on inflammation and micro-circulation. Several pro-inflammatory cyto- and chemokines as well as adhesion molecules are cleared by distinct LIPID-A methods. Moreover, a single LIPID-A can induce proliferative activity of circulating endothelial progenitor cells and by this way, enhance vascular repair capacity. Microcirculation is modified by LIPID-A by influencing the balance of vasoconstrictory and -dilatative mediators, plasma viscosity and erythrocyte aggregation resulting in an activation of functional capillary reserve and blood flow.

MeSH terms

  • Atherosclerosis / blood
  • Atherosclerosis / etiology
  • Atherosclerosis / physiopathology
  • Atherosclerosis / prevention & control*
  • Biomarkers / blood
  • Blood Component Removal*
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / physiopathology*
  • Hemodynamics
  • Humans
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / complications
  • Hypercholesterolemia / physiopathology
  • Hypercholesterolemia / therapy*
  • Inflammation / blood
  • Inflammation / etiology
  • Inflammation / physiopathology
  • Inflammation / prevention & control*
  • Inflammation Mediators / blood*
  • Lipoprotein(a) / blood
  • Lipoproteins, LDL / blood*
  • Microcirculation*
  • Treatment Outcome

Substances

  • Biomarkers
  • Inflammation Mediators
  • Lipoprotein(a)
  • Lipoproteins, LDL