## Objective: Mice deficient in beta2-microglobulin (beta2m), but expressing the human major histocompatibility complex (mhc) class i molecule hla-b27, have been reported to develop spontaneous inflammatory arthritis (sa). we sought to determine whether, under certain conditions, beta2m deficiency
Fine mapping of a major histocompatibility complex in ankylosing spondylitis: Association of the HLA–DPA1 and HLA–DPB1 regions
✍ Scribed by Roberto Díaz-Peña; Ana M. Aransay; Jacome Bruges-Armas; Antonio López-Vázquez; Naiara Rodríguez-Ezpeleta; Iñaki Mendibil; Alejandra Sánchez; Juan Carlos Torre-Alonso; Bruno F. Bettencourt; Juan Mulero; Eduardo Collantes; Carlos López-Larrea
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 307 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0004-3591
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✦ Synopsis
Abstract
Objective
To investigate the potential association of major histocompatibility complex (MHC) markers other than HLA–B27 with ankylosing spondylitis (AS).
Methods
A total of 603 patients with AS and 542 healthy control subjects, all of whom were HLA–B27 positive, were selected for this study based on clinical criteria. First, high‐density genotyping across the MHC region (2,360 single‐nucleotide polymorphisms [SNPs]) was performed in a cohort of 191 patients and 241 control subjects. After a fine‐mapping study, 5 SNPs from the HLA–DPA1/DPB1 region were validated in a second cohort of 412 patients with AS and 301 healthy control subjects.
Results
Seventeen SNPs located within or near the HLA–DPA1 and HLA–DPB1 loci showed association with AS (P = 1.38 × 10^−5^ to 0.05). In addition, multimarker tests, both linkage disequilibrium and sliding windows, showed association of some groups of adjacent SNPs within the HLA–DPA1/DPB1 region with AS (P = 1.0 × 10^−4^ to 3.96 × 10^−7^). We validated the association by genotyping 5 SNPs from the DPA1/DPB1 region in an additional cohort and obtained P values from 6.42 × 10^−5^ to 0.01 in the analysis of the combined cohorts. Subtyping analysis of HLA–DPA1 and HLA–DPB1 showed that HLA–DPA1*01:03, A1*02:01, and B1*13:01 were the subtypes most susceptible to AS.
Conclusion
HLA markers and linkage disequilibrium blocks near HLA–DPA1 and HLA–DPB1 are statistically associated with AS. We identified a region located around the HLA–DPA1 and HLA–DPB1 loci associated with AS, another region within the MHC that is different from HLA–B27.
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