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HLA-DRB1 等位基因对日本成人Still 病患者易感性和临床表现的影响。

Effects of HLA-DRB1 alleles on susceptibility and clinical manifestations in Japanese patients with adult onset Still's disease.

机构信息

Department of Rheumatology, Fukushima Medical University School of Medicine, 1 Hikarigaoka, Fukushima, Fukushima, 960-1295, Japan.

Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, 305-8575, Japan.

出版信息

Arthritis Res Ther. 2017 Sep 12;19(1):199. doi: 10.1186/s13075-017-1406-x.

Abstract

BACKGROUND

HLA-DRB1 alleles are major determinants of genetic predisposition to rheumatic diseases. We assessed whether DRB1 alleles are associated with susceptibility to particular clinical features of adult onset Still's disease (AOSD) in a Japanese population by determining the DRB1 allele distributions.

METHODS

DRB1 genotyping of 96 patients with AOSD and 1,026 healthy controls was performed. Genomic DNA samples from the AOSD patients were also genotyped for MEFV exons 1, 2, 3, and 10 by direct sequencing.

RESULTS

In Japanese patients with AOSD, we observed a predisposing association of DRB115:01 (p = 8.60 × 10, corrected p (Pc) = 0.0002, odds ratio (OR) = 3.04, 95% confidence interval (95% CI) = 1.91-4.84) and DR5 serological group (p = 0.0006, OR = 2.39, 95% CI = 1.49-3.83) and a protective association of DRB109:01 (p = 0.0004, Pc = 0.0110, OR = 0.34, 95% CI = 0.18-0.66) with AOSD, and amino acid residues 86 and 98 of the DRβ chain were protectively associated with AOSD. MEFV variants were identified in 49 patients with AOSD (56.3%). The predisposing effect of DR5 was confirmed only in patients with AOSD who had MEFV variants and not in those without MEFV variants. Additionally, DR5 in patients with AOSD are associated with macrophage activation syndrome (MAS) and steroid pulse therapy.

CONCLUSION

The DRB115:01 and DR5 are both associated with AOSD susceptibility in Japanese subjects. A protective association between the DRB109:01 allele and AOSD was also observed in these patients. Our data also highlight the effects of DRB1 alleles in susceptibility to AOSD.

摘要

背景

HLA-DRB1 等位基因是风湿性疾病遗传易感性的主要决定因素。我们通过确定 DRB1 等位基因的分布,评估了 DRB1 等位基因是否与日本人群成年发病Still 病(AOSD)的特定临床特征的易感性相关。

方法

对 96 例 AOSD 患者和 1026 例健康对照者进行了 DRB1 基因分型。对 AOSD 患者的基因组 DNA 样本还进行了 MEFV 外显子 1、2、3 和 10 的直接测序,以确定 MEFV 基因型。

结果

在日本 AOSD 患者中,我们观察到 DRB115:01(p=8.60×10,校正 p(Pc)=0.0002,比值比(OR)=3.04,95%置信区间(95%CI)=1.91-4.84)和 DR5 血清学组(p=0.0006,OR=2.39,95%CI=1.49-3.83)与 AOSD 存在易感性相关,DRB109:01(p=0.0004,Pc=0.0110,OR=0.34,95%CI=0.18-0.66)与 AOSD 存在保护性相关,DRβ 链的氨基酸残基 86 和 98 与 AOSD 存在保护性相关。在 49 例 AOSD 患者中发现了 MEFV 变异(56.3%)。只有在携带 MEFV 变异的 AOSD 患者中,DR5 的易感性作用才得到确认,而在没有 MEFV 变异的患者中则没有。此外,AOSD 患者中的 DR5 与巨噬细胞活化综合征(MAS)和皮质类固醇脉冲治疗相关。

结论

DRB115:01 和 DR5 均与日本人群的 AOSD 易感性相关。在这些患者中,我们还观察到 DRB109:01 等位基因与 AOSD 之间存在保护性关联。我们的数据还强调了 DRB1 等位基因在 AOSD 易感性中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1703/5596459/325990535eff/13075_2017_1406_Fig1_HTML.jpg

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