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白细胞介素-18基因的一种启动子单倍型与日本人群中的幼年特发性关节炎相关。

A promoter haplotype of the interleukin-18 gene is associated with juvenile idiopathic arthritis in the Japanese population.

作者信息

Sugiura Tomoko, Maeno Nobuaki, Kawaguchi Yasushi, Takei Syuji, Imanaka Hiroyuki, Kawano Yoshifumi, Terajima-Ichida Hisae, Hara Masako, Kamatani Naoyuki

机构信息

Institute of Rheumatology, Tokyo Women's Medical University School of Medicine, 10-22 Kawada-cho, Shinjuku-ku, Tokyo, Japan.

出版信息

Arthritis Res Ther. 2006;8(3):R60. doi: 10.1186/ar1930. Epub 2006 Mar 17.

Abstract

Recently, we reported that genetic polymorphisms within the human IL18 gene were associated with disease susceptibility to adult-onset Still's disease (AOSD), which is characterized by extraordinarily high serum levels of IL-18. Because high serum IL-18 induction has also been observed in the systemic type of juvenile idiopathic arthritis (JIA), we investigated whether similar genetic skewing is present in this disease. Three haplotypes, S01, S02, and S03, composed of 13 genetic polymorphisms covering two distinct promoter regions, were determined for 33 JIA patients, including 17 with systemic JIA, 10 with polyarthritis, and 6 with oligoarthritis. Haplotypes were also analyzed for 28 AOSD patients, 164 rheumatoid arthritis (RA) patients, 102 patients with collagen diseases, and 173 healthy control subjects. The frequency of individuals carrying a diplotype configuration (a combination of two haplotypes) of S01/S01 was significantly higher in the JIA patients, including all subgroups, than in the healthy controls (P = 0.0045, Fischer exact probability test; odds ratio (OR) = 3.55, 95% confidence interval (CI) = 1.55-8.14). In patients with systemic JIA, its frequency did not differ statistically from that of normal controls. Nevertheless, it is possible that haplotype S01 is associated with the phenotype of high IL-18 production in systemic JIA because the patients carrying S01/S01 showed significantly higher serum IL-18 levels compared with patients with other diplotype configurations (P = 0.017, Mann-Whitney U test). We confirmed that the frequency of the diplotype configuration of S01/S01 was significantly higher in AOSD patients than in healthy control subjects (P = 0.011, OR = 3.45, 95% CI = 1.42-8.36). Furthermore, the RA patients were also more predisposed to have S01/S01 (P = 0.018, OR = 2.00, 95% CI = 1.14-3.50) than the healthy control subjects, whereas the patients with collagen diseases did not. In summary, the diplotype configuration of S01/S01 was associated with susceptibility to JIA as well as AOSD and RA, and linked to significantly higher IL-18 production in systemic JIA. Possession of the diplotype configuration of S01/S01 would be one of the genetic risk factors for susceptibility to arthritis in the Japanese population.

摘要

最近,我们报道了人类白细胞介素18(IL18)基因内的遗传多态性与成人斯蒂尔病(AOSD)的疾病易感性相关,该病的特征是血清IL-18水平异常升高。由于在全身型幼年特发性关节炎(JIA)中也观察到血清IL-18诱导水平升高,我们研究了这种疾病中是否存在类似的基因偏态。对33例JIA患者(包括17例全身型JIA、10例多关节炎型和6例少关节炎型)确定了由覆盖两个不同启动子区域的13个遗传多态性组成的三种单倍型,即S01、S02和S03。还对28例AOSD患者、164例类风湿关节炎(RA)患者、102例胶原病患者和173例健康对照者进行了单倍型分析。在包括所有亚组的JIA患者中,携带S01/S01双倍型组合(两种单倍型的组合)的个体频率显著高于健康对照者(P = 0.0045,费舍尔精确概率检验;优势比(OR) = 3.55,95%置信区间(CI) = 1.55 - 8.14)。在全身型JIA患者中,其频率与正常对照者无统计学差异。然而,单倍型S01可能与全身型JIA中高IL-18产生的表型相关,因为携带S01/S01的患者与其他双倍型组合的患者相比,血清IL-18水平显著更高(P = 0.017,曼-惠特尼U检验)。我们证实,AOSD患者中S01/S01双倍型组合的频率显著高于健康对照者(P = 0.011,OR = 3.45,95% CI = 1.42 - 8.36)。此外,RA患者也比健康对照者更易携带S01/S01(P = 0.018,OR = 2.00,95% CI = 1.14 - 3.50),而胶原病患者则不然。总之,S01/S01双倍型组合与JIA以及AOSD和RA的易感性相关,并与全身型JIA中显著更高的IL-18产生有关。拥有S01/S01双倍型组合可能是日本人群中关节炎易感性的遗传风险因素之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fae0/1526617/4b2d59943767/ar1930-1.jpg

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