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. 2022 Jan 5;8(1):e001977. doi: 10.1136/rmdopen-2021-001977

Table 1.

Clinical characteristics of included patients

Total LVV TAK LV-GCA
n=100 n=53 n=47
Age (years) at diagnosis, median (IQR) 48 (29.5–62.5) 31 (23–38) 63 (57–71)
Sex, n (%), Male 22 (22%) 6 (11.3%) 16 (34.0%)
Female 78 (78%) 47 (88.7%) 31 (66.0%)
Newly diagnosed (%) 25 (25%) 6 (11.3%) 19 (40.4%)
Disease activity, n (%), Inactive 57 (57%) 34 (64.2%) 23 (48.9%)
Active 43 (43%) 19 (35.8%) 24 (51.1%)
ESR (mm/hour), median (IQR), missing=1 27 (13–64) 22 (11–40) 33.5 (14–81)
CRP (mg/dL), median (IQR), missing=2 0.84 (0.3–3.1) 0.8 (0.3–2.0) 1.68 (0.3–6.9)
Vascular symptoms, n (%), missing=1 23 (23.2%) 14 (26.4%) 9 (19.6%)
Systemic symptoms, n (%), missing=1 22 (22.2%) 7 (13.2%) 15 (32.6%)
Cranial symptoms, n (%), missing=1 7 (7.1%) 2 (3.8%) 5 (10.9%)
Visual manifestations, n (%), missing=1 2 (2.0%) 1 (1.9%) 1 (2.2%)
Polymyalgia rheumatica, n (%), missing=1 7 (7.1%) 0 (0.0%) 7 (15.2%)
Patients with at least one synchronous stenosis or dilation, n (%) 57 (57%) 34 (64.2%) 23 (48.9%)
Patients with at least one follow-up CTA / MRA performed between 6 and 30 months from baseline PET, n (%) 28 (28%) 20 (37.7%) 8 (17%)
Patients with at least one incident stenosis or dilation, n (%) 4 (14%) 4 (20%) 0 (0%)

Clinical characteristics of the overall LVV population and of the subgroups with TAK and LV-GCA at baseline assessment, and outcome measures.

CRP, C reactive protein; CTA, CT angiography; ESR, erythrocyte sedimentation rate; LV-GCA, large vessel-giant cell arteritis; LVV, large vessel vasculitis; MRA, MR angiography; PET, positron emission tomography; TAK, Takayasu arteritis; WBC, white blood cell.