Abstract

BackgroundAnti-citrullinated protein antibodies (ACPA) are central to rheumatoid arthritis (RA) pathogenesis and may develop at inflamed mucosa. We investigated whether asthma, a disease of airway mucosal inflammation, was associated with elevated ACPA before RA diagnosis.MethodsWe performed a nested case-control study among women in two prospective cohorts, the Nurses’ Health Study (NHS; 1976–2014) and NHSII (1989–2015). Blood was obtained on a subset (NHS: 1989–1990; NHSII: 1996–1999). Cases met 1987 ACR or 2010 ACR/EULAR RA criteria by medical record review and were classified as seropositive (ACPA+ or rheumatoid factor positivity) or seronegative by clinical laboratory testing at diagnosis. We identified RA cases with blood drawn before the date of RA diagnosis (index date), matching each to three controls by age, cohort, year, time from blood draw to index date, and menopause. Pre-RA ACPA elevation for cases was defined as >99th percentile of the control distribution on a research assay composed of autoantibodies targeting citrullinated protein epitopes or positivity on the second-generation commercial assay for cyclic citrullinated peptide. Asthma status and covariates were obtained through biennial questionnaires before blood draw. Conditional logistic regression estimated ORs and 95%CIs for RA by pre-RA ACPA and clinical serostatus, adjusted for matching factors, smoking pack-years, passive smoking, and body mass index (BMI).ResultsWe identified 284 incident RA cases and 849 matched controls; mean age at the index date was 61.2 years (SD 10.1). Blood was drawn 9.7 years (mean; SD 5.8) before the index date. We identified 96 (33.8%) RA cases with elevated pre-RA ACPA. At blood draw, 17.7% of pre-RA ACPA+ cases and 6.3% of matched controls (p = 0.0008) reported clinician-diagnosed asthma. After adjusting for matching factors, smoking pack-years, passive smoking, and BMI, asthma was significantly associated with pre-RA ACPA+ RA (OR 3.57, 95%CI 1.58,8.04). Asthma was not associated with overall RA (OR 1.45, 95%CI 0.91,2.31), but was significantly associated with seropositive RA (OR 1.79, 95%CI 1.01,3.18).ConclusionsAsthma was strongly associated with ACPA elevation in blood drawn prior to RA diagnosis, independent of smoking. Chronic mucosal airway inflammation may contribute to ACPA development and RA pathogenesis.

Highlights

  • The mucosal paradigm for seropositive rheumatoid arthritis (RA) pathogenesis postulates that RA may develop after loss of immune tolerance due to environmental triggers at mucosal surfaces in genetically susceptible individuals [1, 2]

  • We investigated the association between asthma and RA, overall and defined by RA phenotype at the time of blood draw, based on serologic status by medical record review time of clinical diagnosis

  • Study sample Characteristics of the study sample (n = 1133) at the time of blood draw are shown in Table 2 according to pre-RA Anti-citrullinated protein antibodies (ACPA) status by the sensitive definition for RA cases (n = 96) and their matched controls (n = 286)

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Summary

Introduction

The mucosal paradigm for seropositive rheumatoid arthritis (RA) pathogenesis postulates that RA may develop after loss of immune tolerance due to environmental triggers at mucosal surfaces in genetically susceptible individuals [1, 2]. Smoking is an established risk factor for seropositive RA [3, 4]. The biologic effect of smoking or other inhalants (such as cadmium in pollution [5], asbestos [6], silica [7], textile dust [8], coal [9], or diesel fumes [10]) on RA risk may be due to induction of local pulmonary mucosal inflammation at the bronchioles and alveoli, leading to protein citrullination [11] and the aberrant formation of anti-citrullinated protein antibodies (ACPA) in those with the HLA-DRB1 shared epitope [12,13,14,15,16,17,18]. Anti-citrullinated protein antibodies (ACPA) are central to rheumatoid arthritis (RA) pathogenesis and may develop at inflamed mucosa. A disease of airway mucosal inflammation, was associated with elevated ACPA before RA diagnosis

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