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: 2750

Utility of Methotrexate in Polymyalgia Rheumatica

María Laura de la Torre1, Anabella Rodriguez2, Micaela Ana Cosatti3 and Cecilia N. Pisoni4, 1Internal Medicine, Rheumatology and Immunology, CEMIC, Buenos Aires, Argentina, 2Internal Medicine, Hospital General de Agudos “Juan A. Fernández”, Buenos Aires, Argentina, 3Internal Medicine, Rheumatology and Immunology, CEMIC, CABA, Argentina, 4Internal Medicine, CEMIC, Rheumatology and Immunology, CEMIC, Buenos Aires, Argentina

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: Methotrexate (MTX) and polymyalgia rheumatica

  • 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, October 23, 2018

Title: Vasculitis Poster III: Immunosuppressive Therapy in Giant Cell Arteritis and Polymyalgia Rheumatica

Session Type: ACR Poster Session C

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

Background/Purpose:

Polymyalgia rheumatica (PMR) is a frequent inflammatory condition in patients over 50 years old. Nearly 60% of patients experience relapses of the symptoms during steroids tapering and steroids dependency is frequent. There is a need to find other therapeutic options to avoid the risks of long term steroid treatment. Methotrexate (MTX) use in PMR has been studied with contradictory results regarding reduction of relapses.

Our objective was to evaluate the efficacy of MTX to reduce relapses and recurrences in patients with PMR.

Methods:

This is an observational longitudinal cohort study. We included 94 consecutive patients with PMR fulfilling EULAR/ACR 2012 criteria. Clinical symptoms, laboratory results, treatment received and disease course information were extracted from the medical records.

Patients were assigned to 3 groups according to the treatment prescribed by the treating physician. Group 1: treated with steroids alone, group 2: treated with steroids initially and MTX following a relapse or recurrence and group 3: treated with steroids and MTX from diagnosis.

Definitions:

  • Relapse: recurrence of symptoms and an increase of erythrocyte sedimentation rate (ESR) or C reactive protein (CRP) in patients still receiving steroids.
  • Remission: time of discontinuing prednisone.
  • Recurrence: recurrence of the original symptoms and an increase of ESR or CRP after discontinuing prednisone.

We studied predictors of relapse in the total population. To evaluate MTX effect, patients from group 2 were analyzed comparing outcomes during the first period with corticosteroids alone with the second period with steroids and MTX.

Results:

Ninety four patients were included, 77.6% women, mean age 75.6 years old (SD 8.1). The median time of follow up was 21.3 months (IQR 11.7-56.2).

Patients were assigned to one of 3 groups according to their treatment: 53 (56.4%) were treated only with steroids (group 1), 33 (35.1%) received initially steroids and later on MTX (group 2) and 8 (8.5 %) had steroids and MTX from diagnosis (group 3). Table 1 shows a comparison between groups.

We found a tendency of ESR to predict relapses (p 0.07) in the total population.

In group 2, we identified 35 relapses during the period of treatment with steroids alone and only 8 relapses during the period of combined treatment (p 0.0001). MTX reduced the dose of corticosteroids used and reduced the time to remission in this group of patients (Table 2).

Table 1

GROUP 1

GROUP 2

GROUP 3

N

53

33

8

One relapse, n (%)

12 (22.6)

28 (84.8)

4 (50)

More than 1 relapse, n (%)

3 (5.6)

11 (33.3)

2 (25)

Time to the first relapse, months, median (IQR)

9.2 (6.7-10.7)

8.6 (6-14.9)

21.5 (9.6-92.8)

Remission, n (%)

20 (37.7)

14 (42.4)

3 (37.5)

Time to remission, m (IQR)

12.9 (11.8-21.6)

21.2 (15-25.2)

13.3 (12.4-99.8)

Duration of remission, m (SD)

1.8 (0-15.2)

6.6 (2.8-17.6)

19.5 (4.4-40.5)

Recurrence, n (%)

4 (7.5)

11 (33.3)

0 (0)

Total dose of steroids, g, mean (SD)

3.7 (4.8)

5.6 (3.3)

12 (14.6)

Table 2

pre MTX

post MTX

p

Relapses, n

35

8

0.0001

Time to first relapse, months, median (ICR)

13.2 (6.4-16.8)

9.2 (6.2-17.4)

0.12

Time free of relapse, months, median (ICR)

8.6 (5.3-14.9)

7.5 (4.6-17.4)

0.25

Dose of steroids at first relapse, mg/day, mean (SD)

5.1 (2.3)

3 (1.5)

0.02

Remission, n

7

9

0.73

Time to remission, months, median (ICR)

22.9 (18.1-30.1)

8.7 (7-12.2)

0.01

Duration of remission, months, mean (SD)

14.7 (17.4)

13.9(20.9)

0.53

Recurrences, n

7

4

0.36

Conclusion:

The use of MTX in PMR patients who already had a relapse reduces the number of future relapses and reduced the time to achieve remission. Starting MTX allowed a reduction of corticosteroids dose.


Disclosure: M. L. de la Torre, None; A. Rodriguez, None; M. A. Cosatti, None; C. N. Pisoni, None.

To cite this abstract in AMA style:

de la Torre ML, Rodriguez A, Cosatti MA, Pisoni CN. Utility of Methotrexate in Polymyalgia Rheumatica [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/utility-of-methotrexate-in-polymyalgia-rheumatica/. 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 2018 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/utility-of-methotrexate-in-polymyalgia-rheumatica/

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