Patterns of Arterial Disease in Takayasu's Arteritis and Giant Cell Arteritis.
Gribbons KB., Ponte C., Carette S., Craven A., Cuthbertson D., Hoffman GS., Khalidi NA., Koening CL., Langford CA., Maksimowicz-McKinnon K., McAlear CA., Monach PA., Moreland LW., Pagnoux C., Quinn KA., Robson JC., Seo P., Sreih AG., Suppiah R., Warrington KJ., Ytterberg SR., Luqmani R., Watts R., Merkel PA., Grayson PC.
OBJECTIVE: To identify and validate, using computer-driven methods, patterns of arterial disease in Takayasu's arteritis (TAK) and giant cell arteritis (GCA). METHODS: Patients with TAK or GCA were studied from the Diagnostic and Classification Criteria for Vasculitis (DCVAS) cohort and a combined North American (NA) cohort. Case inclusion required evidence of large-vessel involvement, defined as stenosis, occlusion, or aneurysm by angiography/ultrasonography, or increased FDG uptake by positron-emission tomography (PET) in at least one of 11 specified arterial territories. K-means cluster analysis identified groups of patients based on pattern of arterial involvement. Cluster groups were identified in the DCVAS cohort and independently validated in the NA cohort. RESULTS: A total of 1,068 patients were included (DCVAS: TAK=461, GCA=217; NA: TAK=225, GCA=165). Six distinct clusters of patients were identified in DCVAS and validated in the NA cohort. Patients with TAK were more likely to have disease in the abdominal vasculature, bilateral disease of the subclavian and carotid arteries, or focal disease limited to the left subclavian artery than GCA (p<0.01). Patients with GCA were more likely to have diffuse disease, involvement of bilateral axillary/subclavian arteries, or minimal disease without a definable pattern than TAK (p<0.01). Patients with TAK were more likely to have damage by angiography, and patients with GCA were more likely to have arterial FDG-uptake by PET without associated vascular damage. CONCLUSION: Arterial patterns of disease highlight both shared and divergent vascular patterns between TAK and GCA and should be incorporated into classification criteria for large-vessel vasculitis.