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: 1722

What Is the Clinical Utility of MR Imaging in the Management of Nr-Axspa Patients?

Ismail Sari1, Ahmed Omar1, Jonathan Chan2, Mohamed Bedaiwi1, Renise Ayearst1, Nigil Haroon1 and Robert D Inman3, 1Rheumatology, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada, 2Rheumatology, Spondylitis program, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada, 3Immunlogy and Institute of Medical Science, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: anti-TNF therapy, non-radiographic and spondylarthropathy

  • 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: Monday, November 9, 2015

Title: Spondylarthropathies and Psoriatic Arthritis - Comorbidities and Treatment Poster II

Session Type: ACR Poster Session B

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

Background/Purpose: The ASAS classification criteria have provided new insights in the classification of axial spondyloarthropathy (axSpA). MR imaging (MRI) is an intrinsic component of the imaging arm of the classification criteria for non-radiographic (nr)-axSpA. The scheme classifies these patients by the imaging arm if the MRI is positive or by the clinical arm if such MRI evidence is lacking. The current algorithm does not address the clinical utility of MRI in patients who meet the clinical criteria, in which B27 is mandatory. The main aim of our study was to compare clinical features and outcomes of nr-axSpA patients stratified into MRI-Pos, MRI-Neg, and MRI-ND (not done) subsets. The study provided the opportunity to define clinical commonalities and differences between these three subsets, and to address the added value of MRI in the management of nr-axSpA. 

Methods: Patients who met the criteria for nr-axSpA by the imaging arm or the clinical arm were included. Patients who met the NY criteria for AS were excluded.  X-rays and MRIs were scored by two rheumatologists, blinded to clinical diagnosis. Discordant results were settled by a third reader. Patients classified as nr-axSpA were further stratified into the imaging or clinical arms. The clinical arm was further stratified into MRI-Neg and MRI-ND groups. Clinical characteristics were then obtained for each group from the clinical database.

Results: There were 107 patients fulfilling ASAS criteria for nr-axSpA. The median age of the patients was 35.2 (18-64) years, 51.4% were male and 85% were B27+. There were 37 patients in the imaging arm and 70 patients in the clinical arm.  The intraclass correlation coefficient of the readers for right and left SIJ were 0.75 and 0.73 respectively. The kappa value of the readers for MR classification was 0.74. Age, sex distribution and disease duration were similar between the three groups (Table 1). Extra-articular features, acute phase reactants, BASDAI and BASMI were also comparable between the three groups. There were 45 (42.1%) patients who were treated with TNF inhibitors.  Subgroup analysis of the patients who received TNFi treatment showed that biological treatment utilization, biologic switch frequencies, and rates of biologic non-response were similar between the three groups.  

Conclusion: The clinical profiles of nr-axSpA patients with and without MRI confirmation are comparable, including response to biologic therapy. This suggests that there is a degree of homogeneity in the nr-axSpA cohort when patients are classified on clinical grounds alone. Including B27 as a mandatory inclusion criterion likely underlies this homogeneity, and does so to a greater extent than imaging studies.

Table 1: Clinical and demographical characteristics of the groups

 

 

MR(+), n=37

Clinical arm MR(-) n=38

Clinical arm MR ND

 n=32

p

Age (years)

33.9 (18-56)

40.4 (18-64)

37.5 (18-63)

0.42

Disease duration (years)

4 (1.5-28)

11 (1-34)

7 (1-38)

0.15

Sex (M %)

54.1

47.4

53.1

0.82

B27 (%)

56.8

100

100

<0.0001

Smoking (%)

40

29

29.6

0.59

BASFI

2.7 (0-10)

1.9 (0-8)

2.3 (0-7.8)

0.6

BASDAI

4.5 (0.6-9.8)

3 (0-9.2)

3.8 (0-9.2)

0.81

BASMI

2 (0-5)

1 (0-5)

1 (0-2)

0.19

ESR

6.5 (1-122)

5 (1-52)

6.5 (1-63)

0.81

CRP

3 (0-135)

3 (0-38)

3 (0-28)

0.62

Biologic ever (%)

43.2

47.4

34.4

0.54

Biologic switch ever (%)

43.8

44.4

36.4

0.9

Biologic switch, LOE, %

85.7

71.4

75

0.8

NSAIDs, continuous use  (%)

86.4

79.2

71.4

0.48

Arthritis (%)

48.6

47.4

59.4

0.56

Uveitis, %

16.2

28.9

34.4

0.21

Psoriasis, %

13.5

18.4

12.5

0.75

Dactilytis, %

8.1

2.7

6.3

0.59

IBD, %

8.1

2.6

3.1

0.47

Enthesitis, %

33.3

32.1

25

0.76

Family history, %

5.7

22.2

45.2

0.001

Subgroup analysis of the patients receiving TNFi treatment

 

Mr+, n=16

Mr-, n=18

Mr (ND), n=11

p value

Current TNF, %

68.8

55.6

90.9

0.14

Switch ever, %

43.8

44.4

36.4

0.9

Switch, LOE, %

85.7

71.4

75

0.8

Number of switch

2 (1-4)

2 (1-4)

1.5 (1-4)

0.87

ΔBASDAI

-1.5 (-7.8-3.2)

-2.6 (-6.6-3.4)

-3.6 (-4.8-3.8)

0.69

ΔCRP

0 (-23-0)

0 (-10-1)

-2 (-32-0)

0.13

Continous data are presented with median with minimum-maximum values


Disclosure: I. Sari, None; A. Omar, None; J. Chan, None; M. Bedaiwi, None; R. Ayearst, None; N. Haroon, None; R. D. Inman, None.

To cite this abstract in AMA style:

Sari I, Omar A, Chan J, Bedaiwi M, Ayearst R, Haroon N, Inman RD. What Is the Clinical Utility of MR Imaging in the Management of Nr-Axspa Patients? [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/what-is-the-clinical-utility-of-mr-imaging-in-the-management-of-nr-axspa-patients/. 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 2015 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/what-is-the-clinical-utility-of-mr-imaging-in-the-management-of-nr-axspa-patients/

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