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Association of Protective HLA-A With HLA-B*27 Positive Ankylosing Spondylitis

Authors :
Nordin, Jessika
Pettersson, Mats
Rosenberg, Lina Hultin
Mathioudaki, Argyri
Karlsson, Åsa
Murén, Eva
Tandre, Karolina
Rönnblom, Lars
Kastbom, Alf
Cedergren, Jan
Eriksson, Per
Söderkvist, Peter
Lindblad-Toh, Kerstin
Meadows, Jennifer R. S.
Nordin, Jessika
Pettersson, Mats
Rosenberg, Lina Hultin
Mathioudaki, Argyri
Karlsson, Åsa
Murén, Eva
Tandre, Karolina
Rönnblom, Lars
Kastbom, Alf
Cedergren, Jan
Eriksson, Per
Söderkvist, Peter
Lindblad-Toh, Kerstin
Meadows, Jennifer R. S.
Publication Year :
2021

Abstract

Objectives: To further elucidate the role of the MHC in ankylosing spondylitis by typing 17 genes, searching for HLA-B∗27 independent associations and assessing the impact of sex on this male biased disease. Methods: High-confidence two-field resolution genotyping was performed on 310 cases and 2196 controls using an n-1 concordance method. Protein-coding variants were called from next-generation sequencing reads using up to four software programs and the consensus result recorded. Logistic regression tests were applied to the dataset as a whole, and also in stratified sets based on sex or HLA-B∗27 status. The amino acids driving association were also examined. Results: Twenty-five HLA protein-coding variants were significantly associated to disease in the population. Three novel protective associations were found in a HLA-B∗27 positive population, HLA-A∗24:02 (OR = 0.4, CI = 0.2–0.7), and HLA-A amino acids Leu95 and Gln156. We identified a key set of seven loci that were common to both sexes, and robust to change in sample size. Stratifying by sex uncovered three novel risk variants restricted to the female population (HLA-DQA1∗04.01, -DQB1∗04:02, -DRB1∗08:01; OR = 2.4–3.1). We also uncovered a set of neutral variants in the female population, which in turn conferred strong effects in the male set, highlighting how population composition can lead to the masking of true associations. Conclusion: Population stratification allowed for a nuanced investigation into the tightly linked MHC region, revealing novel HLA-B∗27 signals as well as replicating previous HLA-B∗27 dependent results. This dissection of signals may help to elucidate sex biased disease predisposition and clinical progression.<br />Funding agencies: Swedish Research Council, FORMAS (Dnr 2012-1531), Knut and Alice Wallenberg Foundation (Dnr 2012-0268), Swedish Research Council for Medicine and Health (D0283001 and Dnr 2018-02399), the Swedish Rheumatism Association, and King Gustaf V’s 80-year Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1337542772
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.3389.fgene.2021.659042