In a patient suspected of ankylosing spondylitis, which blood test is more important: erythrocyte sedimentation rate (ESR) or high‑sensitivity C‑reactive protein (hs‑CRP)?

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Neither ESR nor hs-CRP is Superior for Diagnosing Ankylosing Spondylitis

Neither ESR nor high-sensitivity CRP should be used as primary screening tests for ankylosing spondylitis, as both have poor sensitivity (~50%) and are not suitable screening parameters. 1 Instead, clinical features (inflammatory back pain) and HLA-B27 testing are the recommended screening tools in primary care. 1

Why Acute Phase Reactants Are Poor Screening Tests

Limited Diagnostic Performance

  • ESR and CRP have only 50% sensitivity in patients with AS and early AS, meaning half of patients with the disease will have normal values 1
  • The post-test probability with elevated ESR/CRP is only about 11-12%, making them unsuitable for screening 1
  • Both markers received an overall rating of "0" (not suitable) as primary screening parameters due to low sensitivity 1

Lack of Superiority Between the Two Tests

  • Multiple studies demonstrate that neither CRP nor ESR is superior to the other for assessing disease activity in AS 2, 3
  • Correlation coefficients between ESR/CRP and disease activity measures (BASDAI, physician assessment) range from only 0.06-0.48, indicating poor to moderate correlation 3
  • In a study of 191 AS patients, sensitivity ranged from 44-100% and specificity from 44-84% for both markers, with no clear advantage of one over the other 3

When to Use Each Marker (If Ordered)

Slight Advantage of CRP in Specific Contexts

  • CRP may be marginally more sensitive and specific than ESR for detecting active disease episodes 4, 5
  • One older study found CRP was significantly elevated in active AS while ESR values were not statistically different between active and inactive disease 5
  • High-sensitivity CRP (hs-CRP) correlates better than routine CRP with clinical disease activity parameters in established AS, particularly in patients with negative routine CRP (<6 mg/L) 6

ESR Considerations

  • ESR correlates with CRP (correlation coefficient ~0.30-0.50) but adds little independent information 2, 3
  • ESR is affected by confounding factors like anemia and azotemia that artificially elevate values 7, 8

Recommended Diagnostic Approach

Primary Screening Parameters (Not Laboratory Tests)

For patients with chronic low back pain >3 months with onset <45 years, use these screening criteria: 1

  1. Inflammatory back pain features (sensitivity 75%, post-test probability 14%):

    • Morning stiffness >30 minutes
    • Pain at night/early morning
    • Improvement with exercise 1
  2. HLA-B27 testing (sensitivity 90%, post-test probability 32%):

    • Only 3 HLA-B27 positive patients need referral to diagnose 1 case of axial SpA
    • This is the ideal screening test with a likelihood ratio of 9 1

Role of Imaging Over Laboratory Tests

  • MRI of sacroiliac joints has 90% sensitivity and 90% specificity, far superior to ESR/CRP 1
  • Sacroiliitis on imaging (X-ray or MRI) in a young patient with chronic back pain is a valid referral criterion 1

Clinical Pitfall to Avoid

Do not rely on normal ESR or CRP to exclude ankylosing spondylitis. With only 50% sensitivity, half of patients with active AS will have normal acute phase reactants. 1 If clinical suspicion is high based on inflammatory back pain features or HLA-B27 positivity, refer to rheumatology regardless of ESR/CRP values. 1

Monitoring vs. Diagnosis Distinction

While ESR and CRP are poor for diagnosis, they may have limited utility for monitoring disease activity in established AS:

  • Multiple studies show modest correlations (0.32-0.68) between CRP and disease activity scores in longitudinal monitoring 1
  • However, many studies also show no significant correlation (NS) between inflammatory markers and clinical measures 1

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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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