Nejentsev Sergey, Laaksonen Mikko, Tienari Pentti J, Fernandez Oscar, Cordell Heather, Ruutiainen Juhani, Wikström Juhani, Pastinen Tomi, Kuokkanen Satu, Hillert Jan, Ilonen Jorma
Department of Virology, University of Turku, Finland.
Hum Immunol. 2003 Mar;64(3):345-9. doi: 10.1016/s0198-8859(02)00825-x.
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 (Lys(469)/Lys(469)) 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 Lys(469) homozygotes (relative risk = 1.3, p = 0.002).
细胞间黏附分子-1(ICAM-1)参与了多发性硬化症(MS)的发病机制,而ICAM-1基因的序列变异可能是MS遗传易感性的原因。我们在芬兰和西班牙的病例、对照及患病家庭中研究了MS与ICAM-1基因13848A>G(K469E)多态性的关联。在这两个人群中均发现AA(Lys(469)/Lys(469))基因型的风险增加。观察到的效应在HLA-DQB1*0602阳性受试者中最为明显,这意味着MS存在遗传异质性。对所有已发表数据集的荟萃分析支持ICAM-1 Lys(469)纯合子患MS的风险增加(相对风险=1.3,p=0.002)。