ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 186

Asthma, Chronic Obstructive Pulmonary Disease, and Subsequent Risk for Incident Rheumatoid Arthritis Among Women: A Prospective Cohort Study

Julia Ford1, Xinyi Liu 1, Su H. Chu 2, Bing Lu 1, Michael Cho 1, Edwin Silverman 1, Karen Costenbader 1, Carlos Camargo 3 and Jeffrey Sparks 1, 1Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Massachusetts General Hospital, Boston, MA

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: asthma and chronic obstructive pulmonary disease, Rheumatoid arthritis (RA)

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 10, 2019

Title: Epidemiology & Public Health Poster I: RA

Session Type: Poster Session (Sunday)

Session Time: 9:00AM-11:00AM

Background/Purpose: While RA patients are known to have excess respiratory morbidity and mortality, less is known about the role of chronic respiratory diseases in the development of RA. Prior studies using retrospective cohort or case-control studies suggest an association between asthma and increased RA risk, but were limited by potential for recall bias and lack of data on smoking and RA serostatus. Chronic obstructive pulmonary disease (COPD) as a risk factor for incident RA has not previously been studied. We investigated whether asthma or COPD are associated with subsequent risk of developing RA, independent of smoking.

Methods: We performed a prospective cohort study investigating asthma, COPD, and incident RA risk in two prospective cohorts, the Nurses’ Health Study (NHS, 1988-2014) and NHSII (1991-2015). Self-reported asthma and COPD were confirmed using validated supplemental respiratory questionnaires. Medical record review determined incident RA (meeting 1987 ACR or 2010 ACR/EULAR criteria), serostatus, and date of diagnosis. Covariates including smoking pack-years were self-reported every 2 years. Two separate pooled analyses were performed: 1) asthma as primary exposure, and 2) COPD as primary exposure, each compared to women who never reported asthma or COPD. Cox regression models estimated hazard ratios (HR) and 95% confidence intervals (CI) for RA (overall and by serostatus), adjusting for smoking and other potential confounders. We performed subgroup analyses among never and ever smokers and by age to evaluate possible effect modification for asthma and RA risk by smoking and age.

Results: We identified 1,060 incident RA cases (63% seropositive) during 4,384,471 person-years of follow-up. In the asthma analysis, the RA incident rate (IR) for 15,148 women with validated asthma was 0.38 per 1000 person-years compared to an IR of 0.23 per 1000 person-years for women without asthma or COPD. Asthma was associated with increased risk for all RA (HR 1.53, 95%CI 1.24, 1.88) compared to no asthma/COPD after adjusting for covariates including continuous pack-years and smoking status (Table 1). Among never-smokers, asthma was associated with increased risk for all RA (HR 1.53, 95%CI 1.14, 2.06) and seronegative RA (HR 1.91, 95%CI 1.22, 2.97), but not seropositive RA. In the COPD analysis, the RA IR for 3,573 women with validated COPD was 0.66 per 1000 person-years. COPD was associated with increased risk of all RA (HR 1.89, 95%CI 1.31, 2.75) and seropositive RA (HR 2.07, 95%CI 1.31, 3.25) after adjusting for covariates including continuous pack-years and smoking status (Table 2). The association of COPD with seropositive RA was most pronounced in the subgroup of ever-smokers who were >55 years old (HR 2.71, 95%CI 1.55,4.76).

Conclusion: In this large prospective cohort study, asthma and COPD were both associated with increased risk for incident RA, independent of smoking status/intensity. Identifying asthma and COPD patients as at-risk populations for RA can help develop prevention and screening strategies as well as provide insight into the role of chronic airway inflammation in RA pathogenesis.


Disclosure: J. Ford, None; X. Liu, None; S. Chu, None; B. Lu, None; M. Cho, GlaxoSmithKline, 2, Genentech, 5; E. Silverman, GlaxoSmithKline, 2, 9; K. Costenbader, Astra-Zeneca, 2, Glaxo Smith Kline, 2, Janssen Scientific Affairs, LLC, 2, Lupus Foundation of America, 2, Lupus Research Alliance, 2, Merck, 2; C. Camargo, None; J. Sparks, None.

To cite this abstract in AMA style:

Ford J, Liu X, Chu S, Lu B, Cho M, Silverman E, Costenbader K, Camargo C, Sparks J. Asthma, Chronic Obstructive Pulmonary Disease, and Subsequent Risk for Incident Rheumatoid Arthritis Among Women: A Prospective Cohort Study [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/asthma-chronic-obstructive-pulmonary-disease-and-subsequent-risk-for-incident-rheumatoid-arthritis-among-women-a-prospective-cohort-study/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2019 ACR/ARP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/asthma-chronic-obstructive-pulmonary-disease-and-subsequent-risk-for-incident-rheumatoid-arthritis-among-women-a-prospective-cohort-study/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology