Abstract

ObjectiveTo investigate the risk of immune-mediated inflammatory diseases (IMIDs) in patients with ankylosing spondylitis (AS).MethodsUsing 2003–2012 claims data from the Taiwanese National Health Insurance Research Database, we identified 30,911 newly diagnosed AS patients requiring medical therapy from 2006 to 2012. In addition, we randomly selected 309,110 non-AS individuals matching (1:10) the AS patients with regard to age, sex and the year of the index date. After excluding subjects with the corresponding prior IMIDs, we calculated the incidence rates (IRs) of various IMIDs in the AS and non-AS cohorts and estimated the hazard ratios (HRs) with 95% confidence intervals after adjusting for age, sex, the Charlson comorbidity index, the frequency of ambulatory visits during the follow-up period and medications. We conducted sensitivity analyses by excluding those who developed IMIDs within 3 months after the index date.ResultsIn the follow-up period, we found that newly diagnosed AS patients had significantly increased risks of acute anterior uveitis, psoriasis, Sjögren’s syndrome, thromboangiitis obliterans, Behcet’s disease and sarcoidosis. However, the risk of Sjögren’s syndrome did not increase in AS patients in the sensitivity analysis. In the same period, this study found no significant differences in the risks of Crohn’s disease, ulcerative colitis, systemic lupus erythematosus, systemic sclerosis, dermatomyositis, polymyositis, pemphigus and vitiligo between newly diagnosed AS patients and non-AS individuals. AS patients had a significantly reduced risk of rheumatoid arthritis.ConclusionNewly diagnosed Taiwanese AS patients had increased risks of acute anterior uveitis, psoriasis, thromboangiitis obliterans, Behcet’s disease and sarcoidosis, but a reduced risk of rheumatoid arthritis.

Highlights

  • Immune-mediated inflammatory disease (IMID) is a term that covers a group of disorders characterised by altered immune regulation causing chronic inflammation in targeted organs or systems

  • The present study aimed to investigate the incidences of various IMIDs, including SpA concept-related EAMs (i.e. acute anterior uveitis (AAU), psoriasis, Crohn’s disease (CD) and ulcerative colitis (UC)), systemic lupus erythematosus (SLE), Sjögren’s syndrome (SS), rheumatoid arthritis (RA), systemic sclerosis (SSc), polymyositis (PM), dermatomyositis (DMtis), thromboangiitis obliterans (TAO), Behcet’s disease (BD), sarcoidosis, pemphigus and vitiligo in a Taiwanese nationwide ankylosing spondylitis (AS) cohort compared with a matched non-AS cohort, using the National Health Insurance Research Database (NHIRD)

  • Multivariable Cox regression analyses for the associations between AS and the development of IMIDs after the index date Crude and multivariable Cox regression analyses for the relative risks of various IMIDs occurring after the index date in AS patients when compared with non-AS individuals are shown in Additional file 1: Table S1

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Summary

Introduction

Immune-mediated inflammatory disease (IMID) is a term that covers a group of disorders characterised by altered immune regulation causing chronic inflammation in targeted organs or systems. Chen et al Arthritis Research & Therapy (2019) 21:196 articular manifestations, acute anterior uveitis (AAU), psoriasis and inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), are most strongly associated with AS [11]. To our knowledge, no prior study had concurrently assessed the risks of developing various IMIDs in addition to SpA concept-related IMIDs (i.e. AAU, psoriasis, CD and UC) among AS patients. The present study aimed to investigate the incidences of various IMIDs, including SpA concept-related EAMs (i.e. AAU, psoriasis, CD and UC), systemic lupus erythematosus (SLE), Sjögren’s syndrome (SS), rheumatoid arthritis (RA), systemic sclerosis (SSc), polymyositis (PM), dermatomyositis (DMtis), thromboangiitis obliterans (TAO), Behcet’s disease (BD), sarcoidosis, pemphigus and vitiligo in a Taiwanese nationwide AS cohort compared with a matched non-AS cohort, using the NHIRD

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