What is polymyalgia rheumatica (PMR)?

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Last updated: April 29, 2025View editorial policy

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From the Guidelines

Polymyalgia rheumatica (PMR) should be treated with low-dose corticosteroids, specifically prednisone starting at 12.5-25 mg daily, with a gradual taper over 1-2 years, and regular monitoring of symptoms and inflammatory markers (ESR and CRP) to guide treatment adjustments, as recommended by the 2015 European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) collaborative initiative 1.

Key Considerations

  • The initial prednisone dose should be based on the patient's risk factors for relapse and side effects, with a higher dose (up to 25 mg daily) recommended for patients with a higher risk of relapse and a lower dose (12.5 mg daily) for patients with a higher risk of side effects 1.
  • Methotrexate may be added as a steroid-sparing agent, particularly in patients with a high risk of relapse or side effects, as it has been shown to be effective in reducing the cumulative glucocorticoid dose and improving outcomes in PMR patients 1.
  • Regular monitoring of symptoms and inflammatory markers (ESR and CRP) is essential to guide treatment adjustments and minimize the risk of relapse and side effects 1.
  • Patients with PMR should be educated on the importance of exercise and lifestyle modifications to manage their condition and prevent complications 1.

Treatment Algorithm

  • Initial treatment: prednisone 12.5-25 mg daily, with a gradual taper over 1-2 years 1.
  • Monitoring: regular assessment of symptoms and inflammatory markers (ESR and CRP) to guide treatment adjustments 1.
  • Steroid-sparing agents: methotrexate may be added in patients with a high risk of relapse or side effects 1.
  • Relapse therapy: increase dose to the previously effective dose, and consider adding methotrexate if not already used 1.

Prognostic Factors

  • Female sex, high ESR, and peripheral inflammatory arthritis have been associated with a higher risk of relapse and prolonged therapy in some studies, but the evidence is not consistent across all studies 1.
  • Patients with these risk factors may require closer monitoring and more aggressive treatment to minimize the risk of relapse and side effects.

From the Research

Treatment of Polymyalgia Rheumatica

  • The primary treatment for polymyalgia rheumatica (PMR) is corticosteroids, with prednisone being the most commonly used steroid 2, 3, 4.
  • The initial dose of prednisone is typically 10-20 mg/day, which yields clinical improvement in the majority of patients with PMR within 7 days 3, 4.
  • Methotrexate is often used as a corticosteroid-sparing agent, particularly in patients with relapses or those at high risk for steroid-related toxicity 2, 3, 5, 4.
  • The use of methotrexate has been shown to reduce the cumulative prednisone dose and allow for shorter prednisone treatment 2, 5.

Disease Management

  • The main goals of PMR treatment are to induce remission and prevent relapse 6.
  • Patients with isolated PMR typically experience a rapid response to prednisone treatment, with remission achieved in most patients at a dose of 15 mg/d 4.
  • Relapses are not uncommon when the dose of prednisone is reduced to 5 mg/day or lower 3.
  • Methotrexate is the most commonly used disease-modifying antirheumatic drug for PMR management, although its effect is often modest 6.

Alternative Therapies

  • Anti-interleukin-6 receptor antibody tocilizumab has shown efficacy in PMR in case series and retrospective studies, but controlled trials are needed to fully establish its efficacy 6.
  • Janus-kinase inhibitors may have a potential beneficial effect in PMR, but further research is needed to determine their efficacy 6.
  • Antitumor necrosis factor agents are not supported by randomized controlled trials for use in PMR 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Medical management of polymyalgia rheumatica.

Expert opinion on pharmacotherapy, 2010

Research

Treatment of polymyalgia rheumatica: a systematic review.

Archives of internal medicine, 2009

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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