| Literature DB >> 33327594 |
Patricia Castro-Santos1,2, Jordi Olloquequi1, Ricardo A Verdugo3,4, Miguel A Gutiérrez5,6, Carmen Pinochet7, Luis A Quiñones8,9, Roberto Díaz-Peña1.
Abstract
HLA-DRB1 shared epitope (SE) alleles are important genetic contributors for the risk of developing anti-citrullinated protein antibodies (ACPA)-positive rheumatoid arthritis (RA), particularly in Caucasians. We aimed to analyze the contribution of HLA-DRB1 alleles and single nucleotide polymorphisms (SNPs) within the major histocompatibility complex (MHC) region to the susceptibility to develop ACPA-positive RA in a Latin American (LA) population with admixed ancestry. A total of 289 ACPA-positive RA patients and 510 controls were enrolled in this study. The presence of HLA-DRB1*04:01, *09:01 and *10:01 was increased in ACPA-positive RA patients compared with healthy controls (p < 0.0001, p < 0.001 and p < 0.01, respectively), whereas DRB1*07:01 and *08:02 was associated with a decreased risk of ACPA-positive RA (p < 0.001 and p < 0.01, respectively). These results showed a strong correlation with estimates from studies in Asians but not in Caucasian populations. The present study describes the protective effects of the HLA-DRB1*07:01 and *08:02 alleles in ACPA-positive RA patients in a LA population for the first time. Identifying relationships between HLA-DRB1 alleles and RA is important for identifying disease associations in different ethnic groups in order to reach a better understanding of RA worldwide.Entities:
Keywords: ACPA; HLA; HLA-DRB1; Latin American; admixed population; rheumatoid arthritis
Year: 2020 PMID: 33327594 DOI: 10.3390/biology9120467
Source DB: PubMed Journal: Biology (Basel) ISSN: 2079-7737