Abstract

Both reactive arthritis (ReA) and undifferentiated spondyloarthritis (uSpA) belong to the group of autoinflammatory diseases called spondyloarthritis (SpA). Hypotheses have been proposed about a relationship between the intestinal mucosa and inflammation of joint tissues. The role of immunoglobulin IgA or secretory immunoglobulin A (SIgA) in the inflammatory and/or clinical activity of patients with SpA remains poorly understood. To evaluate the status of total IgA and SIgA, and the association among the levels of SIgA, IgA, IgA anti-Chlamydia trachomatis, and anti-Shigella spp. with the disease activity measures, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) levels, was compared in a cohort of patients with ReA and uSpA and healthy subjects. This was a cross-sectional study. The serum concentrations of SIgA, IgA anti-C. trachomatis, anti-Shigella spp., and total IgA were measured. Disease activity was measured in each patient by means of Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS). Statistical analysis did include as bivariate evaluation, comparisons by Student's t-test, Kruskal-Wallis test, and U Mann-Whitney test, with a multivariate evaluation by principal components analysis (PCA). A correlation analysis was carried out using the Pearson correlation coefficient and a linear regression models. All analysis were made using Stata version 11.2® for Windows, R V3.3.21. Statistical significance was defined a p-value <0.05. In all, 46 patients (78.2% men; mean age, 34.8 ± 12.3 years) and 53 controls (41% men; mean age, 32 ± 11.4 years) were included in the study. The mean serum levels of SIgA were higher in SpA patients than in healthy subjects (p < 0.001). Only SIgA levels correlated with disease activity: BASDAI (r = -0.42, p = 0.0046), ASDAS-CRP (r = -0.37, p = 0.014), and ASDAS-ESR (r = -0.45, p = 0.0021). The negative correlation between SIgA and all activity indices was higher in HLA-B27-positive patients (BASDAI r = -0.70, p = 0.0009, ASDAS-CRP r = -0.58, p = 0.0093, and ASDAS-ESR r = -0.57, p = 0.0083). The PCA showed three factors: the first component was constituted by variables referred as clinical activity measures, the second did include the serological activity markers, and the last component was compounded by age and symptoms time. Elevated serum levels of SIgA were found to be related with low disease activity in patients with ReA and uSpA.

Highlights

  • Spondyloarthritis (SpA) comprises a group of rheumatic diseases including ankylosing spondylitis (AS), arthritis/spondylitis with inflammatory bowel disease (IBD), psoriatic arthritis (PsA), reactive arthritis (ReA), and undifferentiated spondyloarthritis

  • We investigated the correlation of Secretory immunoglobulin A (SIgA), total IgA, IgA anti-C. trachomatis, and IgA anti-Shigella spp. with disease activity measurements and the erythrocyte sedimentation rate (ESR) and serum levels C-reactive protein (CRP) [43, 44]

  • We found that for every 1 μg/ ml increase of SIgA, the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) disease activity measurements decreased by about 0.12 units, the Ankylosing Spondylitis Disease Activity Score (ASDAS)-CRP decreased by about 0.4 units, and the ASDAS-ESR decreased by about 0.048 units

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Summary

Introduction

Spondyloarthritis (SpA) comprises a group of rheumatic diseases including ankylosing spondylitis (AS), arthritis/spondylitis with inflammatory bowel disease (IBD), psoriatic arthritis (PsA), reactive arthritis (ReA), and undifferentiated spondyloarthritis (uSpA). ReA is a spondyloarthropathic disorder characterized by inflammation of the joints and tissues occurring after gastrointestinal or genitourinary infections, where the arthritic process is generated about 3–4 weeks postinfectious, because of the short time of symptoms (days or weeks), many extra-articular features such as gastrointestinal involvement may not be clearly identified in the clinical setting. No differences were found in the mean concentration of serum SIgA in relation to the status of the HLA-B27 allele (p = 0.83) in SpA patients. No association was observed in the levels of SIgA with respect to osteomuscular symptoms, fatigue, or medical history (data not shown)

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