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首发外周关节炎的强直性脊柱炎患者的临床和遗传学特征。

Clinical and genetic characteristics of ankylosing spondylitis patients with peripheral arthritis at disease onset.

机构信息

Department of Rheumatology, IDIPHIM University Hospital Puerta de Hierro Research Institute, Madrid, Spain.

I+D Department, Progenika Biopharma SA, Bizkaia, Spain.

出版信息

Clin Exp Rheumatol. 2019 Mar-Apr;37(2):215-221. Epub 2018 Sep 17.

Abstract

OBJECTIVES

The aim of this study was to assess the clinical and genetic characteristics associated with the presence of peripheral arthritis (PA) at disease onset in patients with ankylosing spondylitis (AS).

METHODS

456 Spanish AS patients, diagnosed according to the modified New York Criteria, who had at least ten years of follow-up since initial disease onset were selected from the National Spondyloarthropathies Registry (REGISPONSER). 18.9% of AS patients initially presented PA. Clinical variables and 384 single nucleotide polymorphisms (SNPs) distributed in 190 genes were analysed. SNP genotyping was performed using the Illumina GoldenGate genotyping platform. Association tests for allele frequencies and for categorical clinical variables were performed by the χ2 test and with the unpaired t-test for continuous variables. p-values of <0.05 were considered statistically significant.

RESULTS

AS patients with PA showed an earlier age of disease onset (p=0.021), longer disease duration (p=0.020) and longer duration of AS symptoms from onset (p=0.034) than AS patients without PA. We found significant associations with the presence of PA at disease onset in 14 SNPs located in 10 genes: HLA-DQB2 (rs2857210 and rs9276615), HLA-DOB (rs2857151, rs2621332 and rs1383261), JAK2 (rs7857730), IL-23R (rs11209008 and rs10489630), CYP1B1 (rs1056836), NELL1 (rs8176786), KL (rs564481), and MEFV (rs224204), IL-2RB (rs743777) and IL-1A (rs1800587).

CONCLUSIONS

Both clinical and genetic factors are associated with the presence of PA at disease onset in Spanish AS patients. The results suggest that this subset of AS patients with PA at disease onset might have differentiation factors involved in disease pathogenesis.

摘要

目的

本研究旨在评估与强直性脊柱炎(AS)患者发病时出现外周关节炎(PA)相关的临床和遗传特征。

方法

从国家脊柱关节病登记处(REGISPONSER)中选择了 456 名西班牙 AS 患者,这些患者根据改良的纽约标准诊断,自疾病初始发作以来至少有 10 年的随访。18.9%的 AS 患者最初出现 PA。分析了临床变量和分布在 190 个基因中的 384 个单核苷酸多态性(SNP)。SNP 基因分型使用 Illumina GoldenGate 基因分型平台进行。通过 χ2 检验和未配对 t 检验对等位基因频率和分类临床变量进行关联检验。p 值<0.05 被认为具有统计学意义。

结果

PA 发病的 AS 患者发病年龄更小(p=0.021)、疾病持续时间更长(p=0.020)、从发病到出现 AS 症状的持续时间更长(p=0.034)。我们发现,在 10 个基因中的 14 个 SNP 中存在与发病时 PA 存在显著相关的位置:HLA-DQB2(rs2857210 和 rs9276615)、HLA-DOB(rs2857151、rs2621332 和 rs1383261)、JAK2(rs7857730)、IL-23R(rs11209008 和 rs10489630)、CYP1B1(rs1056836)、NELL1(rs8176786)、KL(rs564481)、MEFV(rs224204)、IL-2RB(rs743777)和 IL-1A(rs1800587)。

结论

临床和遗传因素均与西班牙 AS 患者发病时出现 PA 相关。这些结果表明,发病时存在 PA 的这组 AS 患者可能具有涉及发病机制的分化因素。

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