Table 1

Clinical characteristics of the patients with and without GCA

Demographic, clinical and laboratory characteristicsTMIILANEG
Number4277
Age at disease onset, median (IQR), years78 (69–80)70 (65–82)75 (68–78)
Males/females, n9/333/44/3
Any cranial symptoms*, n (%)41 (98)7 (100)5 (71)
Any visual symptoms†, n (%)8 (19)3 (43)3 (43)
Systemic signs/symptoms‡, n (%)31 (74)4 (57)3 (43)
Polymyalgia rheumatica, n (%)13 (31)1 (14)2 (29)
ESR, median (IQR), mm/hour90 (74–116)38 (7–102)30 (24–44)
CRP, median (IQR), mg/dL§8.35 (3.83–15.70)6.73 (1.63–13.18)1.06 (0.22–1.41)
Prednisone at TABs, n (%)0 (0)4 (57)0 (0)
  • *At least one of the following: headache, scalp tenderness, jaw claudication.

  • †At least one of the following: sight loss, diplopia, amaurosis fugax.

  • ‡At least one of the following: fever, fatigue, anorexia, weight loss of at least 4 kg.

  • §Upper limit of the normal reference range=0.5 mg/dL.

  • CRP, C reactive protein; ESR, erythrocyte sedimentation rate; GCA, giant cell arteritis; ILA, inflammation limited to adventitia; NEG, normal temporal artery biopsies without inflammation from patients without GCA; TAB, temporal artery biopsy; TMI, transmural inflammation.