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: 2880

Clinical Evolution of Patients with Inflammatory Back Pain: A Population-Based Longitudinal Cohort Study

Runsheng Wang1, Cynthia S. Crowson2, Kerry Wright3 and Michael Ward4, 1Rheumatology, Columbia University Medical Center, New York, NY, 2Health Sciences Research, Mayo Clinic College of Medicine and Science, Rochester, MN, 3Rheumatology, Mayo Clinic, Rochester, MN, 4NIH/NIAMS, Bethesda, MD

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Ankylosing spondylitis (AS), inflammatory back pain, longitudinal studies, population studies and spondylarthritis

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

Date: Tuesday, November 7, 2017

Title: Spondyloarthropathies and Psoriatic Arthritis – Clinical Aspects and Treatment IV

Session Type: ACR Concurrent Abstract Session

Session Time: 4:30PM-6:00PM

Title: Clinical Evolution of Patients with Inflammatory Back Pain: a Population-Based Longitudinal Cohort Study

Authors: Runsheng Wang1, Cynthia Crowson2, Kerry Wright2, Michael Ward3

1.       Columbia University Medical Center, New York, NY

2.       Mayo Clinic, Rochester, MN

3.       NIH/NIAMS, Bethesda, MD

Background/Purpose:   Inflammatory back pain (IBP) is an early manifestation and a key feature of spondyloarthritis (SpA).  However the natural history of IBP has not been well defined.  Significant differences exist between the prevalence of IBP (3-6%) and prevalence of SpA (0.5-1%), suggesting either that IBP often resolves or is due to conditions other than SpA.  The objective of this study was to investigate the long-term outcomes of IBP, and clinical predictors of progression to SpA.    

Methods: A population-based cohort of patients with incident IBP in 2000-2003 among residents of a geographically defined area was established retrospectively. Using diagnostic codes for back pain on clinic visits, we screened and validated the presence of new-onset IBP among patients age 16 to 35 via manual medical record review.  Verified patients either met the Calin, Berlin, or ASAS criteria, or were considered by their treating rheumatologist to have IBP. We collected data on clinical SpA features, HLA-B27 status, inflammatory markers, and imaging, and followed their outcomes until July 2016. Aalen-Johansen methods (a multistate generalization of cumulative incidence with adjustment for competing risks) were used to examine their evolution to one of 3 outcomes: progression to SpA, progression to a non-SpA diagnosis, or resolution of back pain. Recursive partitioning with a time to event outcome was used to identify predictors for progression to SpA.    

Results:   After screening 5304 patients, we identified 124 subjects with new-onset IBP from 2000 to 2003.  After a median of 13.2 years of follow up, progression to SpA occurred in 39 patients (Figure).  The probability of having SpA at 5, 10, 15 years was 24%, 30%, and 33%, respectively.  In almost half of the patients, their IBP resolved during follow up.  Progression was seen in 85% of 13 patients with a history of uveitis, and 26% of 111 patients without history of uveitis by 15 years after IBP incidence.  Among those without a history of uveitis, progression was seen in 32% of men and 14% of women by 15 years.     

Conclusion:   Less than 1/3 of patients with new-onset IBP progress to SpA over more than a decade of follow up, while many resolve.  History of uveitis is the most important predictor for progression. 

Figure. Progression from IBP to SpA, non-SpA conditions, back pain resolved, and persistent back pain. 


Disclosure: R. Wang, None; C. S. Crowson, None; K. Wright, None; M. Ward, None.

To cite this abstract in AMA style:

Wang R, Crowson CS, Wright K, Ward M. Clinical Evolution of Patients with Inflammatory Back Pain: A Population-Based Longitudinal Cohort Study [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/clinical-evolution-of-patients-with-inflammatory-back-pain-a-population-based-longitudinal-cohort-study/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/clinical-evolution-of-patients-with-inflammatory-back-pain-a-population-based-longitudinal-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