Giant cell arteritis: laboratory predictors of a positive temporal artery biopsy

Matthew D Walvick1, Michael P Walvick

  • 1PGY-2 Internal Medicine, University of California San Francisco-Fresno, Fresno, California 93701, USA. mwalvick@gmail.com

Ophthalmology
|January 15, 2011
PubMed

Insights

C-reactive protein (CRP) and thrombocytosis are significant predictors of a positive temporal artery biopsy in giant cell arteritis. Elevated CRP and platelet counts are more strongly associated with positive biopsies than erythrocyte sedimentation rate.

Area of Science:

  • Rheumatology
  • Internal Medicine
  • Pathology

Background:

  • Giant cell arteritis (GCA) is a systemic vasculitis affecting large and medium-sized arteries.
  • Temporal artery biopsy (TAB) is a key diagnostic tool for GCA.
  • Identifying reliable predictors of a positive TAB is crucial for timely diagnosis and treatment.

Purpose of the Study:

  • To identify laboratory predictors associated with a positive temporal artery biopsy.
  • To evaluate the predictive value of erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and platelet count for GCA diagnosis.

Main Methods:

  • Retrospective cross-sectional study utilizing electronic health records from 1997-2006.
  • Analysis of 3001 patients who underwent TAB.
  • Calculation of odds ratios for ESR, CRP, and platelet count in relation to positive TAB results.

Main Results:

  • A positive TAB was associated with an erythrocyte sedimentation rate (ESR) between 47-107 mm/hr (OR 1.5).
  • A C-reactive protein (CRP) level >2.45 mg/dL increased the odds of a positive TAB by 5.3 times.
  • Platelet count >400,000/μL was associated with 4.2 times greater odds of a positive TAB.

Conclusions:

  • CRP levels >2.45 mg/dL are significant predictors of a positive TAB in GCA.
  • CRP and thrombocytosis (elevated platelet count) appear to be stronger predictors of a positive TAB than ESR.
  • These findings support the utility of CRP and platelet count in the diagnostic workup of suspected GCA.
Abstract

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