What are the signs and symptoms, diagnosis, and treatment of Polymyalgia Rheumatica (PMR)?

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Polymyalgia Rheumatica: Signs, Symptoms, Diagnosis, and Treatment

Clinical Presentation

PMR presents with bilateral shoulder pain and morning stiffness in patients over 60 years old, typically with dramatically elevated inflammatory markers. 1

Key Signs and Symptoms:

  • Bilateral shoulder girdle pain with severe morning stiffness (hallmark feature) 2
  • Neck and hip girdle involvement (though hip involvement is not mandatory for diagnosis) 3, 2
  • Age >60 years (average onset 73 years) 4
  • Acute or subacute onset of symptoms 4
  • Possible hand and knee swelling 1

Red Flags for Atypical Presentation (Requiring Specialist Referral):

  • Age <60 years 1
  • Peripheral inflammatory arthritis 1
  • Systemic symptoms 1
  • Low or normal inflammatory markers 1

Diagnostic Workup

Start with ESR and CRP measurement—both are elevated in >90% of PMR cases, with ESR being the preferred long-term monitoring marker. 5, 4

Essential Laboratory Tests:

  • ESR and CRP (typically markedly elevated; ESR >40 mm/hr associated with higher relapse risk) 1, 5, 6
  • Rheumatoid factor and anti-CCP antibodies to exclude rheumatoid arthritis 3
  • Creatine kinase (CK) to rule out inflammatory myositis 1

Additional Testing to Exclude Mimics:

  • Antinuclear antibodies (ANA) 1
  • ANCA or tuberculosis tests if clinically indicated 1
  • Chest radiographs at physician discretion 1

Imaging Considerations:

  • Ultrasound of affected joints can aid diagnosis 1, 4
  • MRI may be helpful in uncertain cases 4

Comorbidity Assessment Before Starting Glucocorticoids:

  • Hypertension, diabetes, glucose intolerance 1, 3
  • Cardiovascular disease, dyslipidemia 1, 3
  • Osteoporosis (particularly recent fractures) 1, 3
  • Peptic ulcer disease 1, 3
  • Cataracts or glaucoma risk factors 1
  • Chronic or recurrent infections 1

Note: Female sex is associated with higher risk of both glucocorticoid side effects and disease relapse. 1, 3

Treatment

Initiate prednisone at 12.5-25 mg daily—this is the evidence-based starting range that balances efficacy with safety. 1, 3

Initial Dosing Strategy:

  • Use 12.5-25 mg prednisone equivalent daily as starting dose 1
  • Choose higher end (20-25 mg) for patients with high relapse risk (female sex, ESR >40 mm/hr, peripheral arthritis) and low adverse event risk 1, 3
  • Choose lower end (12.5-15 mg) for patients with diabetes, osteoporosis, glaucoma, or other glucocorticoid risk factors 1
  • Never use initial doses ≤7.5 mg/day (inadequate) or >30 mg/day (excessive adverse effects) 1

Tapering Protocol:

Phase 1 (Initial Tapering):

  • Taper to 10 mg/day within 4-8 weeks 1

Phase 2 (Slow Tapering):

  • Decrease by 1 mg every 4 weeks (or 1.25 mg using alternate-day schedules like 10/7.5 mg) until discontinuation 1
  • Tapering slower than 1 mg/month reduces relapse rates 7

Relapse Management:

  • Increase to pre-relapse dose 1
  • Gradually decrease back to the dose where relapse occurred over 4-8 weeks 1

Alternative Glucocorticoid Formulations:

  • Intramuscular methylprednisolone (120 mg every 3 weeks) is an acceptable alternative to oral prednisone 1
  • Modified-release prednisone (10 mg at bedtime) may provide better IL-6 suppression than morning dosing 8
  • Single daily dose preferred over divided doses, except for prominent night pain during low-dose tapering 1

Glucocorticoid-Sparing Agents:

Consider methotrexate early in specific situations: 1

  • Relapses or prolonged therapy anticipated 1
  • High risk of glucocorticoid-related adverse effects 1
  • PMR refractory to glucocorticoid therapy 1

Methotrexate dosing: 10 mg/week or higher shows efficacy 7

NSAIDs:

Do NOT use NSAIDs as primary treatment for PMR—glucocorticoids are strongly preferred. 1

  • NSAIDs may be used short-term for pain from other conditions 1
  • Mild arthritis may respond to NSAIDs alone 1

Monitoring Schedule

Follow patients every 4-8 weeks in year 1, every 8-12 weeks in year 2, and as needed thereafter. 1

At Each Visit Document:

  • Disease activity and pain scores 1
  • ESR and CRP 1
  • Evidence of glucocorticoid side effects 1
  • Comorbidity status 1

Expected Treatment Duration:

  • Typically 2-3 years, but may be longer 4
  • Some patients require <1 year if low baseline ESR and rapid response 6

Common Pitfalls

Beware of partial responders: Patients with persistently elevated IL-6 despite ESR improvement and higher baseline pain scores may require longer treatment duration and higher cumulative glucocorticoid doses. 6

Screen for giant cell arteritis: Approximately 20% of PMR patients develop GCA, and up to two-thirds of GCA patients have PMR symptoms—maintain high vigilance for new headache, jaw claudication, or visual symptoms. 4

Ensure rapid access to care: Patients need direct access to healthcare providers to report flares and adverse events promptly. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Polymyalgia rheumatica--diagnosis and classification.

Journal of autoimmunity, 2014

Guideline

Polymyalgia Rheumatica Diagnosis and Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Diagnostics and treatment of polymyalgia rheumatica].

Zeitschrift fur Rheumatologie, 2016

Guideline

ESR as a Preferred Marker for Polymyalgia Rheumatica

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Corticosteroid requirements in polymyalgia rheumatica.

Archives of internal medicine, 1999

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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