Catalán Diego, Soto Lilian, Neira Óscar, Cuéllar-Gutiérrez María C, Díaz-Peña Roberto, Aravena Octavio, Palou Eduard, Carrascal Montserrat, Aguillón Juan C, Maggi Jaxaira
Immune Regulation and Tolerance Research Group (IRT Group), Programa Disciplinario de Inmunología, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
Sección Reumatología, Departamento de Medicina Interna, Hospital Clínico de la Universidad de Chile, Santiago, Chile.
Front Immunol. 2025 May 13;16:1594723. doi: 10.3389/fimmu.2025.1594723. eCollection 2025.
Rheumatoid arthritis (RA) is an autoimmune disease influenced by genetic factors, particularly alleles. The objective of this study was to characterize the distribution of alleles in Chilean RA patients and healthy controls (HC) and evaluate associations with susceptibility or protection, autoantibody seropositivity, and disease activity.
We genotyped 367 RA patients and 623 HC for using PCR-SSO. Then, we examined allele frequencies and distribution, including known RA risk alleles of the "Shared Epitope" (SE) of HLA-DRB1 and protective (PR) alleles, using the Chi-square or Fisher's exact tests. Odds ratios with 95% confidence intervals were calculated to measure the degree of association, and unpaired T-tests were used to compare continuous variables.
The most frequent SE alleles among RA patients were * (16.1%), * (13.9%), and * (11.7%). SE alleles *, *, *, *, and *, along with non-SE alleles * and *, were associated with RA susceptibility. In addition, allele * showed an association with the presence of anti-cyclic citrullinated peptides (anti-CCP) antibodies. Meanwhile, PR alleles * (14.8%) and * (9.8%) were observed most frequently in HC and RA patients, respectively. PR alleles *, *, and *, as well as the non-PR alleles *, *, *, *, and *, were associated with protection from RA, and showed no significant associations with autoantibody seropositivity.
This study provides a comprehensive overview of allele distribution in the Chilean population, identifying both well-known and novel allele associations with RA susceptibility, protection, and disease activity.
类风湿性关节炎(RA)是一种受遗传因素影响的自身免疫性疾病,尤其是等位基因。本研究的目的是描述智利RA患者和健康对照(HC)中等位基因的分布情况,并评估其与易感性或保护性、自身抗体血清阳性以及疾病活动度的关联。
我们使用聚合酶链反应-序列特异性寡核苷酸探针(PCR-SSO)对367例RA患者和623例HC进行基因分型。然后,我们使用卡方检验或Fisher精确检验来检查等位基因频率和分布,包括HLA-DRB1“共享表位”(SE)的已知RA风险等位基因和保护性(PR)等位基因。计算95%置信区间的比值比以衡量关联程度,并使用非配对t检验比较连续变量。
RA患者中最常见的SE等位基因是*(16.1%)、(13.9%)和(11.7%)。SE等位基因*、、、和,以及非SE等位基因和与RA易感性相关。此外,等位基因与抗环瓜氨酸肽(抗CCP)抗体的存在相关。同时,PR等位基因(14.8%)和*(9.8%)分别在HC和RA患者中最常观察到。PR等位基因*、和,以及非PR等位基因*、、、和与预防RA相关,且与自身抗体血清阳性无显著关联。
本研究全面概述了智利人群中等位基因的分布情况,确定了与RA易感性、保护性和疾病活动度相关的知名和新的等位基因关联。