Table 1

Baseline characteristics

GCA+* (n=53)GCA−* (n=80)P value
Age (years), mean (SD)72.4 (8.8)68.1 (8.5)0.64
Female, n (%)35 (66.0)50 (62.5)0.68
Clinical, n (%)
 Morning stiffness in shoulders26 (49.1)34 (42.5)0.34
 Sudden visual loss13 (24.5)13 (16.3)0.24
 Jaw claudication21 (39.6)5 (6.3)<0.001
 New temporal headache45 (84.9)57 (71.3)0.07
 Scalp tenderness27 (50.9)25 (31.3)0.02
 Abnormal examination of the temporal artery27 (50.9)16 (21.3)<0.001
Laboratory, n (%)
 Maximum ESR ≥50 mm/hour28 (52.8)16 (20.0)<0.001
 Maximum CRP ≥10 mg/liter44 (83.0)36 (45.0)<0.001
 High ESR (≥50 mm/hour) or CRP (≥10 mg/L)47 (88.7)38 (47.5)<0.001
TAB and imaging, n (%)
 TAB performed8 (15.1)3 (3.8)
  Definitive vasculitis on TAB7 (13.2)0 (0.0)0.001
 Ultrasound performed52 (98.1)80 (100)
  Halo sign on temporal artery ultrasound37 (69.8)1 (1.3)<0.001
 Positive TAB or halo sign on temporal artery ultrasound40 (75.5)1 (1.3)<0.001
 FDG-PET/CT performed31 (58.5)32 (40.0)
  FDG-PET activity throughout aorta7 (13.2)1 (1.3)<0.001
 MRA performed29 (54.7)31 (38.8)
 Bilateral axillary involvement on imaging16 (30.2)1 (1.3)<0.001
  Bilateral axillary involvement on ultrasound12 (22.6)1 (1.3)<0.001
  Bilateral axillary involvement on FDG-PET11 (20.8)0 (0.0)<0.001
  • Definitions of classification criteria were used as described in the 2022 ACR/EULAR classification criteria.1

  • *Diagnosis after 6 months of follow-up according to the treating physician.

  • ACR, American College of Rheumatology; CRP, C reactive protein; ESR, Erythrocyte Sedimentation Rate using Westergren method; FDG, fluorodeoxyglucose; GCA−, Patients suspected of but not diagnosed with giant cell arteritis; GCA, giant cell arteritis; GCA+, Patients diagnosed with giant cell arteritis; MRA, magnetic resonance angiography; PET, positron emission tomography; TAB, temporal artery biopsy.