IL-1 genes in myasthenia gravis:: IL-1A-889 polymorphism associated with sex and age of disease onset

被引:17
|
作者
Sciacca, FL
Ferri, C
Veglia, F
Andreetta, F
Mantegazza, R
Cornelio, F
Franciotta, D
Piccolo, G
Cosi, V
Batocchi, AP
Evoli, A
Grimaldi, LME
机构
[1] AUSL2, Dept Neurosci, Caltanissetta, Italy
[2] Natl Neurol Inst, Neuromusc Dis Dept, Milan, Italy
[3] Ist Sci San Raffaele, Neuroimmunol Unit, I-20132 Milan, Italy
[4] Inst Sci Interchange Fdn, Turin, Italy
[5] C Mondino Fdn, Neurol Inst, Pavia, Italy
[6] Catholic Univ, Dept Neurol, Rome, Italy
关键词
interleukin-1; polymorphism; myasthenia gravis; age of onset;
D O I
10.1016/S0165-5728(01)00449-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Myasthenia gravis (MG) is a multifactorial autoimmune disease of the neuromuscular junction. We investigated the relation between four polymorphisms of the interleukin (IL)-1 gene cluster on 2q12-22, and MG susceptibility and clinical features in a large cohort of individuals. No polymorphism was associated with MG susceptibility. However, the IL-1A - 889 CC genotype was associated with early disease onset (p = 0.0044) in the whole MG group and the subgroup of CC males developed MG about 18 years earlier than males carrying other IL-1A - 889 genotypes (p = 0.022). This finding suggests that IL-1A is a disease modifier in MG. or is in linkage disequilibrium with an unknown locus on chromosome 2. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:94 / 99
页数:6
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