Family history of cardiovascular events and endothelial dysfunction in children with familial hypercholesterolemia

Atherosclerosis. 2002 Jul;163(1):193-7. doi: 10.1016/s0021-9150(02)00003-5.

Abstract

Objectives: in patients with familial hypercholesterolemia (FH), the propensity towards atherosclerosis may vary considerably. In the general population, a positive family history is associated with an increased risk for cardiovascular events. Since endothelial dysfunction is predictive for future cardiovascular events, we evaluated whether FH-children with a positive family history of premature cardiovascular disease have more pronounced endothelial dysfunction compared to children with a negative family history.

Study design: 50 FH children, 10-18 years, participated in this study. Thirty-one children had a positive family history for cardiovascular events (fh(+)) and 19 children had no events in the family (fh(-)). Nineteen matched siblings participated as controls. Endothelial function was assessed by testing the flow mediated dilatation (FMD) of the brachial artery.

Results: baseline characteristics were comparable for fh(+), fh(-) and controls. Lipid levels were significantly higher in FH children. In FH, FMD was impaired compared to controls (11.7+/-4.4 vs. 15.6+/-6.8%, P<0.03). In addition, FMD was significantly lower in fh(+) compared to fh(-) (10.7+/-9.9 vs. 13.3+/-4.6%, P<0.05).

Conclusion: In FH-children, endothelial function is impaired compared to matched controls. This impairment is most pronounced in FH children with a positive family history of premature cardiovascular disease.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Adult
  • Age Distribution
  • Blood Flow Velocity
  • Cardiovascular Diseases / epidemiology*
  • Cardiovascular Diseases / genetics*
  • Case-Control Studies
  • Child
  • Endothelium, Vascular / physiopathology*
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Hyperlipoproteinemia Type II / epidemiology*
  • Hyperlipoproteinemia Type II / genetics*
  • Incidence
  • Male
  • Netherlands / epidemiology
  • Pedigree
  • Probability
  • Reference Values
  • Risk Assessment
  • Sex Distribution
  • Statistics, Nonparametric