Association between the HLA-DRB1 with the disease activity parameters among Egyptian RA patients
Rheumatoid factor (RF) and anti-cyclic citrullinated peptide (ACCP), key markers of seropositivity in rheumatoid arthritis (RA), have been linked to the HLA-DRB1 allele. This study aimed to determine the prevalence of HLA-DRB1 in RA patients in tertiary hospitals and assess its association with disease severity. A total of 47 patients diagnosed according to the 2010 EULAR/ACR criteria were enrolled in this cross-sectional study. Participants underwent comprehensive clinical assessments, laboratory investigations—including RF, ACCP, CRP, ESR, liver enzymes, and HLA-DRB1 genotyping via PCR—and were evaluated using the DAS28-CRP score. Results showed that patients positive for HLA-DRB1 had significantly higher DAS28-CRP scores, elevated CRP, RF, and ACCP levels, and increased counts of swollen and tender joints compared to HLA-DRB1-negative individuals. Despite these findings, there was no statistically significant difference in disease activity classification between the two groups. Univariate logistic regression revealed a strong association between disease severity and elevated inflammatory markers. Multivariate analysis identified CRP >6 mg/L as the most significant independent predictor of moderate to severe disease (OR = 144.000, 95% CI: 11.589–178.248, P = 0.001). In conclusion, the presence of HLA-DRB1 is associated with more severe RA, reflected by higher inflammatory markers and joint involvement. However, no association was observed between HLA-DRB1 and extra-articular manifestations or comorbid conditions.
Authors
- Ali S. Mohamed (ORCID: https://orcid.org/0000-0001-8623-6345)
- Fatma Mohamed Badr
- Dahlia A. Hussein
- Mostafa Mahmoud Elnakib
Institutions
- Rheumatology Consultants (US)
- Center for Rheumatology (US)
Publication Details
- Journal
- ARCADEs of MEDICINE
- Published
- 2025-08-30
- DOI
- https://doi.org/10.21608/arcmed.2025.405779.1148
- Primary Topic
- Systemic Lupus Erythematosus Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00