Linkage and association analysis of genes encoding cytokines and myelin proteins in multiple sclerosis

被引:51
作者
He, B [1 ]
Xu, C [1 ]
Yang, B [1 ]
Landtblom, AM [1 ]
Fredrikson, S [1 ]
Hillert, J [1 ]
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Neurol, S-14186 Huddinge, Sweden
关键词
candidate genes; cytokines; linkage; multiple sclerosis; myelin proteins;
D O I
10.1016/S0165-5728(98)00003-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Several genetic factors are likely to play a role in the etiology of multiple sclerosis (MS). We used a candidate gene strategy in a study of polymorphic markers within or close to genes encoding cytokines (interferon-gamma (IFN-gamma), interleukin-2 (IL-2), IL-4, IL-4 receptor (IL-4R), IL-10, transforming growth factor-beta 1 and -beta 2) and myelin proteins (2',3'-cyclic-nucleotide 3'-phosphohydrolase (CNP:ase), myelin associated glycoprotein, oligodendrocyte myelin glycoprotein, proteolipid protein) in 34 Swedish multiplex MS families and in 147 sporadic MS patients and 95 healthy controls. No evidence for linkage was observed in two-point Linkage analysis. However, a slightly positive LOD score of 0.88 (theta = 0.01) for IFN-gamma was found. Affected pedigree member (APM) analysis indicated a possible Linkage with TGF-beta 2 (p = 0.008) and IL-4R (p = 0.043). None of the cytokine markers were associated with MS in case-control analysis. Our results suggest a possible importance of the TGF-beta 2, IL-4R and IFN-gamma genes in MS. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:13 / 19
页数:7
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