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Updated: Aug 2, 2026

Analysis of Physiologic E-Selectin-Mediated Leukocyte Rolling on Microvascular Endothelium
Published on: February 11, 2009
Circulating soluble E-selectin levels and the Ser 128Arg polymorphism in individuals from different ethnic groups
Michelle A Miller1, Sally M Kerry, Yanbin Dong
1Department of Community Health Sciences, St George's Hospital Medical School, Cranmer Terrace, London SW17 ORE, UK. mmiller@sghms.ac.uk
The E-selectin gene Ser128 Arg polymorphism is less frequent in people of African origin, who have lower coronary heart disease risk. This polymorphism did not affect soluble E-selectin levels in this multiethnic study.
Area of Science:
- Genetics
- Cardiovascular Disease
- Immunology
Background:
- A prior study linked the Ser128 Arg polymorphism in the E-selectin gene to coronary heart disease (CHD) in white individuals.
- The E-selectin gene plays a role in inflammatory processes relevant to vascular disease.
Purpose of the Study:
- To investigate the association between the E-selectin gene Ser128 Arg polymorphism and soluble E-selectin levels.
- To examine these associations in a multiethnic population.
Main Methods:
- Genotyping for the E-selectin Ser128 Arg polymorphism (A to C mutation) was performed.
- Plasma soluble E-selectin levels were measured.
- The study included healthy individuals of white, African, and South Asian origin.
Main Results:
- The A to C mutation frequency was significantly lower in individuals of African origin (3.7%) compared to white (9.6%) and South Asian (7.9%) individuals (p=0.005).
- No significant association was found between the E-selectin gene polymorphism and plasma soluble E-selectin levels across all ethnic groups.
Conclusions:
- The lower frequency of the Ser128 Arg polymorphism in people of African origin aligns with their lower CHD risk.
- The polymorphism is not associated with circulating soluble E-selectin levels.
- Further research is needed to determine if this polymorphism influences vascular disease risk through mechanisms other than soluble E-selectin levels, potentially involving leukocyte recruitment.
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