Donn R P, Barrett J H, Farhan A, Stopford A, Pepper L, Shelley E, Davies N, Ollier W E, Thomson W
Arthritis Research Campaign Epidemiology Unit, Manchester, UK.
Arthritis Rheum. 2001 Apr;44(4):802-10. doi: 10.1002/1529-0131(200104)44:4<802::AID-ANR136>3.0.CO;2-G.
To investigate the involvement of candidate cytokine genes in the pathogenesis of juvenile idiopathic arthritis (JIA).
Single nucleotide polymorphisms and intragenic microsatellite markers within 8 candidate cytokine genes (interleukin-1alpha [IL-1alpha], IL-2, IL-4, IL-6, IL-10, interferon-alpha1 [IFNA1], interferon-gamma [IFNG], and interferon regulatory factor 1 [IRF-1]) were investigated in 417 Caucasian patients with clinically characterized JIA and a panel of 276 unrelated, healthy Caucasian controls, all from the United Kingdom.
A novel 3'-untranslated region (3'UTR) polymorphism in IRF-1 was found to be associated with susceptibility to JIA (corrected P = 0.002). No significant association with IL-1alpha, IL-2, IL-4, IL-6, IL-10, IFNA1, or IFNG was observed.
An association between JIA and a previously unreported 3'UTR polymorphism of IRF-1 was observed. This association was not found to be specific to any particular JIA subgroup. This suggests that IRF-1 may contribute to a common pathogenesis shared by all JIA patients, regardless of clinical phenotype. This is most likely to be a genetic contribution to the chronic inflammatory process that underlies JIA pathology.
研究候选细胞因子基因在幼年特发性关节炎(JIA)发病机制中的作用。
对417例具有临床特征的白种人JIA患者以及一组276名来自英国的无亲缘关系的健康白种人对照者,研究8个候选细胞因子基因(白细胞介素-1α [IL-1α]、IL-2、IL-4、IL-6、IL-10、干扰素-α1 [IFNA1]、干扰素-γ [IFNG]和干扰素调节因子1 [IRF-1])内的单核苷酸多态性和基因内微卫星标记。
发现IRF-1基因一个新的3'-非翻译区(3'UTR)多态性与JIA易感性相关(校正P = 0.002)。未观察到与IL-1α、IL-2、IL-4、IL-6、IL-10、IFNA1或IFNG有显著关联。
观察到JIA与IRF-1基因一个先前未报道的3'UTR多态性之间存在关联。未发现这种关联对任何特定的JIA亚组具有特异性。这表明IRF-1可能参与了所有JIA患者共有的发病机制,而不考虑临床表型。这很可能是对JIA病理基础的慢性炎症过程的一种遗传贡献。