Apheresis-inducible cytokine pattern change in children with homozygous familial hypercholesterolemia

Transfus Apher Sci. 2013 Jun;48(3):391-6. doi: 10.1016/j.transci.2013.04.024. Epub 2013 May 4.

Abstract

Familial hypercholesterolemia is a genetic disorder that leads to severe atherosclerosis related cardiovascular complications in young adults. Extracorporeal elimination is a method of LDL-lowering procedures effective in patients with homozygous or severe heterozygous FH utilized in cases. The recruitment of leucocytes into the arterial intima is dependent on a cascade of events mediated through a diverse family of adhesion molecules. Several pro-inflammatory adhesion molecules are cleared by various lipid apheresis methods. This study showed that, LDL-apheresis led to several changes in circulating inflammatory factors which induced antiinflammatory and antiatherogenic changes in the plasma profile in homozygous familial hypercholesterolemic patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Atherosclerosis
  • Blood Component Removal / methods*
  • Child
  • Cholesterol, LDL / blood*
  • Cytokines / metabolism*
  • Female
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Homozygote
  • Humans
  • Hyperlipoproteinemia Type II / genetics*
  • Hyperlipoproteinemia Type II / therapy*
  • Inflammation
  • Lipoproteins, LDL / metabolism
  • Male

Substances

  • Cholesterol, LDL
  • Cytokines
  • Lipoproteins, LDL