ESR vs CRP for Polymyalgia Rheumatica (PMR)
Both ESR and CRP should be measured in the diagnostic evaluation of PMR, with CRP being a more sensitive indicator of current disease activity, though ESR is a superior predictor of relapse. 1, 2
Diagnostic Value of ESR and CRP in PMR
Initial Diagnosis
- Both ESR and CRP are important inflammatory markers in the diagnostic workup for PMR 3, 1
- Laboratory evaluation should include:
- Complete blood count
- ESR and CRP
- Rheumatoid factor
- Anti-cyclic citrullinated peptide antibodies
- Basic biochemistry 1
Comparative Sensitivity
- CRP is more sensitive than ESR for detecting current disease activity:
- Only 1% of PMR patients have normal CRP at diagnosis
- 6% of PMR patients may have normal ESR at diagnosis 2
- CRP is elevated in 62% of relapse episodes where ESR is normal 2
Clinical Scenarios and Special Considerations
PMR with Normal Inflammatory Markers
- PMR can present with normal ESR (≤30 mm/h) in approximately 6-14% of patients 4, 2
- Patients with normal ESR but PMR typically:
- When ESR is normal, CRP is still elevated in 90% of these cases 2
- In rare cases where both ESR and CRP are normal (14% in one study), serum amyloid A (SAA) may be elevated and can be used as an alternative marker 4
Monitoring Disease Activity and Predicting Relapse
- ESR >40 mm/h at diagnosis has twice the relative risk (4.9) for predicting relapse compared to CRP >7.8 mg/dL (relative risk 2.1) 2
- CRP normalizes more quickly than ESR with effective treatment, making it more responsive to short-term changes in disease activity 2, 6
Recommendations for Clinical Practice
Initial Diagnosis:
- Measure both ESR and CRP as part of the diagnostic workup
- Do not exclude PMR diagnosis based on normal ESR alone
- Consider ultrasound to demonstrate bursitis in patients with normal inflammatory markers 4
Disease Monitoring:
- Use both ESR and CRP for monitoring disease activity
- CRP is preferred for assessing immediate treatment response
- ESR is more valuable for predicting long-term outcomes and relapse risk 2
Follow-up Schedule:
- Monitor patients every 4-8 weeks in the first year
- Every 8-12 weeks in the second year
- Assess both clinical response and inflammatory markers 1
Pitfalls to Avoid
- Excluding PMR diagnosis solely based on normal ESR
- Failing to measure both ESR and CRP in the initial workup
- Not considering alternative inflammatory markers (like SAA) when both ESR and CRP are normal in clinically suspicious cases
- Relying exclusively on inflammatory markers without clinical correlation
Remember that response to low-dose glucocorticoids (15-20 mg/day of prednisone) with significant improvement within 24-72 hours remains a key confirmatory element of PMR diagnosis, regardless of baseline inflammatory marker levels 1, 7.