Abstract
Intercellular adhesion molecule-1 (ICAM-1) is involved in the pathogenesis of multiple sclerosis (MS), whereas sequence variations in the ICAM-1 gene could potentially be responsible for the genetic susceptibility to MS. We studied an association of MS with the 13,848A>G (K469E) polymorphism of the ICAM-1 gene in Finnish and Spanish cases and controls and affected families. An increased risk for the AA (Lys469/Lys469) genotype was found in both populations. The effect observed was found to be strongest among the HLA-DQB1*0602-positive subjects, which implies genetic heterogeneity of MS. Meta-analysis of all published datasets supports increased risk of MS for the ICAM-1 Lys469 homozygotes (relative risk = 1.3, p = 0.002). © American Society for Histocompatibility and Immunogenetics, 2003. Published by Elsevier Science Inc.
Author supplied keywords
Cite
CITATION STYLE
Nejentsev, S., Laaksonen, M., Tienari, P. J., Fernandez, O., Cordell, H., Ruutiainen, J., … Ilonen, J. (2003). Intercellular adhesion molecule-1 K469E polymorphism: Study of association with multiple sclerosis. Human Immunology, 64(3), 345–349. https://doi.org/10.1016/S0198-8859(02)00825-X
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.