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: 2145

Age At Onset Determines Severity and  choice of Treatment in Early Rheumatoid Arthritis

Lena Innala1, Bozena Möller2, Lotta Ljung3, Torgny Smedby4, Anna Södergren5, Staffan Magnusson6, Ewa H. Berglin5, Solbritt M. Rantapää-Dahlqvist7 and Solveig Wållberg-Jonsson5, 1Rheumatology, Institution of Public health and clinical medicine/ Rheumatology, University of Umeå, Rheumatology, Sweden, Umeå, Sweden, 2Department of Rheumatology, Sunderby Hospital, Luleå, Sweden, 3Clinical epidemiology unit, Karolinska Institutet, Stockholm, Sweden, 4Department of Rheumatology, Östersund hospital, Östersund, Sweden, 5Rheumatology, Institution of Public health and clinical medicine/ Rheumatology, University of Umeå, Umeå, Sweden, 6Department of Internal Medicine, Sundsvall Hospital, Sundsvall, Sweden, 7Department for Public Health and Clinical Medicine/ Rheumatology, Umeå University, Umeå, Sweden

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: rheumatoid arthritis, treatment and severity

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Title: Rheumatoid Arthritis - Clinical Aspects III: Infections/Risk Factors for Incident Rheumatoid Arthritis/Metrology/Classification/Biomarkers/Predictors of Rheumatolid Arthritis Activity & Severity

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Mortality is increased in rheumatoid arthritis (RA). Contributing factors are disease activity/severity and comorbidity. A relationship between age at onset and pharmacological treatment has been implicated. We evaluated the impact of age at onset on prognostic risk factors and given treatment  during five years from disease onset. 

Methods:

All patients from the 4 most northern counties of Sweden diagnosed with RA (<12 months symptoms) are consecutively included in a large survey on the progress of the disease and its co-morbidies. Up till now 950 (649f, 301m) patients have been included. Median age at disease onset was 58 years (range 18-89). All patients have been followed on a regular basis; a survey of co-morbidities was made at inclusion and after 5 years, measures of disease activity (ESR, CRP, tender joints, swollen joints, VAS pain and VAS global, DAS28, HAQ) and X-ray of hands (erosions, Larsen score) were assessed regularly. Disease severity (extraarticular disease, rheumatoid nodules), co-morbidities and pharmacological treatment (DMARDs, corticosteroids, biologics, NSAIDs, COX2-inhibitors) were registered. Autoantibodies (RF, ANA, ACPAs) and genetic markers (HLA-shared epitope, PTPN22 T-variant) were analysed. Young (YORA)/late (LORA) onset of RA was defined as below/above median age (58 years) at disease onset. Data analyses were based on stratification of the patients in YORA  and LORA.

Results:

Patients with LORA had higher ESR (34.3 vs. 26.0 mm/h, p<0.001), VAS global (47.8 vs. 42.9, p=0.085) and HAQ (1.0 vs 0.8, p=0.075) at baseline and significantly higher accumulated disease activity (AUC for DAS28) at 6 (p=10.0), 12 (p<0.01) and 24 months (p<0.05) compared to YORA. Patients with YORA had more often ACPAs (72.4% vs 65%; p<0.01) and PTPN22 T-variant (37,8 vs 29.5, p=0.056). Presence of extraarticular disease was similar however nodules tended to be more common at young onset (p=0.069) and YORA had significantly higher Larsen score (p<0.001 at 0 and 24 mo). Patients with LORA were significantly more often treated with corticosteroids (77.5 vs. 68.8%; p<0.01), significantly less with methotrexate (81.9 vs. 90.2%; p<0.01) and with biologics (7.6 vs. 24.9%, <0.001). Patients with YORA were treated with DMARDs earlier (within 3 months from inclusion; 94.0% vs. 85.8%; p<0.01) and overall (98.9 vs. 96.7, p=0.05). NSAID was more common in the early onset group (90 vs. 75.9%, p<0.001) with no difference for COX2 inhibitors. 

Conclusion:

Patients with young onset of RA presented with more risk factors for poor prognosis but those with late onset had higher disease activity. YORA were treated with more DMARDs in early disease whilst those with LORA were treated more often with corticosteroids. This may have implications for development of co-morbidities.


Disclosure:

L. Innala,
None;

B. Möller,
None;

L. Ljung,
None;

T. Smedby,
None;

A. Södergren,
None;

S. Magnusson,
None;

E. H. Berglin,
None;

S. M. Rantapää-Dahlqvist,
None;

S. Wållberg-Jonsson,
None.

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2012 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/age-at-onset-determines-severity-and-choice-of-treatment-in-early-rheumatoid-arthritis/

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