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and * Alleles Confer a Protective Effect Against ACPA-Positive Rheumatoid Arthritis in a Latin American Admixed Population. | LitMetric

AI Article Synopsis

  • Shared epitope (SE) alleles are linked to a higher risk of developing anti-citrullinated protein antibodies (ACPA)-positive rheumatoid arthritis (RA), especially in Caucasian populations.
  • The study involved 289 ACPA-positive RA patients and 510 healthy controls from a Latin American (LA) population, revealing that certain HLA-DRB1 alleles and SNPs were associated with either an increased or decreased risk of ACPA-positive RA.
  • Findings suggest protective effects from specific alleles in LA populations, contributing to a broader understanding of RA across different ethnic groups and highlighting the need to explore genetic variations in disease susceptibility globally.

Article Abstract

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 , and was increased in ACPA-positive RA patients compared with healthy controls ( < 0.0001, < 0.001 and < 0.01, respectively), whereas and was associated with a decreased risk of ACPA-positive RA ( < 0.001 and < 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 and alleles in ACPA-positive RA patients in a LA population for the first time. Identifying relationships between alleles and RA is important for identifying disease associations in different ethnic groups in order to reach a better understanding of RA worldwide.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765073PMC
http://dx.doi.org/10.3390/biology9120467DOI Listing

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