Gender- and age-dependent relationships between the E-selectin S128R polymorphism and coronary artery calcification

D L Ellsworth1, L F Bielak, S T Turner

  • 1Division of Epidemiology and Clinical Applications, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Drive MSC 7934, Bethesda, MD 20892-7934, USA. ellsworth@nih.gov

Journal of Molecular Medicine (Berlin, Germany)
|July 24, 2001
PubMed

Insights

The E-selectin S128R gene polymorphism is linked to coronary artery calcification (CAC) in younger women. This finding suggests the E-selectin 128R allele may be an early atherosclerosis risk factor in this demographic.

Area of Science:

  • Cardiovascular disease research
  • Genetics and molecular biology
  • Immunology and inflammation

Background:

  • Atherosclerosis development involves leukocyte adhesion to the vascular endothelium via cell adhesion molecules.
  • A specific polymorphism in the endothelial-leukocyte adhesion molecule 1 (E-selectin) gene (S128R) is associated with severe atherosclerotic disease.
  • This polymorphism affects E-selectin's ligand binding and increases cellular adhesion.

Purpose of the Study:

  • To investigate the association between the E-selectin S128R polymorphism and coronary artery calcification (CAC) in asymptomatic adults.
  • To determine if this genetic variation is a risk factor for atherosclerosis, particularly in younger individuals.

Main Methods:

  • The study examined 294 women (40-88 years) and 314 men (30-80 years) from the Epidemiology of Coronary Artery Calcification Study.
  • Coronary artery calcification (CAC) was detected using noninvasive electron beam computed tomography.
  • Statistical analyses adjusted for traditional cardiovascular risk factors.

Main Results:

  • No association was found between the E-selectin polymorphism and CAC in men of any age or women over 50.
  • In women aged 50 or younger, the E-selectin S128R polymorphism was significantly associated with the presence of CAC.
  • This association remained significant after adjusting for age, BMI, blood pressure, cholesterol levels, and smoking status.

Conclusions:

  • The E-selectin 128R allele may represent a risk factor for coronary atherosclerosis in younger, asymptomatic women.
  • This finding is notable as younger women often have fewer traditional risk factors and different adhesion molecule expression patterns.
  • Further research is warranted to understand the role of E-selectin genetics in early atherosclerosis development in specific demographics.

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