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Arterial lesions in giant cell arteritis: A longitudinal study
Authors:Tanaz A. Kermani  Sehriban Diab  Antoine G. Sreih  David Cuthbertson  Renée Borchin  Simon Carette  Lindsy Forbess  Curry L. Koening  Carol A. McAlear  Paul A. Monach  Larry Moreland  Christian Pagnoux  Philip Seo  Robert F. Spiera  Kenneth J. Warrington  Steven R. Ytterberg  Carol A. Langford  Peter A. Merkel  Nader A. Khalidi
Affiliation:1. Division of Rheumatology, University of California Los Angeles, 2020 Santa Monica Boulevard, Suite 540 Santa Monica, CA 90404;2. Division of Rheumatology, St. Joseph’s Healthcare, McMaster University, Hamilton, ON, Canada;3. Division of Rheumatology, University of Pennsylvania, Philadelphia, PA;4. Department of Biostatistics and Informatics, Department of Pediatrics, University of South Florida, Tampa, FL;5. Division of Rheumatology, Mount Sinai Hospital, Toronto, ON, Canada;6. Division of Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA;7. Division of Rheumatology, University of Utah, Salt Lake City, UT;8. Section of Rheumatology, Boston University School of Medicine, Boston, MA;9. Division of Rheumatology, University of Pittsburgh, Pittsburgh, PA;10. Division of Rheumatology, Johns Hopkins University, Baltimore, MD;11. Division of Rheumatology, Hospital for Special Surgery, New York, NY;12. Division of Rheumatology, Mayo Clinic College of Medicine, Rochester, MN;13. Department of Rheumatic and Immunologic Diseases, Cleveland Clinic, Lerner College of Medicine, Cleveland, OH;14. Division of Rheumatology and the Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA
Abstract:

Objectives

To evaluate large-vessel (LV) abnormalities on serial imaging in patients with giant cell arteritis (GCA) and discern predictors of new lesions.

Methods

Clinical and imaging data from patients with GCA (including subjects diagnosed by LV imaging) enrolled in a prospective, multicenter, longitudinal study and/or a randomized clinical trial were included. New arterial lesions were defined as a lesion in a previously unaffected artery.

Results

The study included 187 patients with GCA, 146 (78%) female, mean (±SD) age at diagnosis 68.5 ± 8.5 years; 39% diagnosed by LV imaging. At least one arterial lesion was present in 123 (66%) on the first study. The most frequently affected arteries were subclavian (42%), axillary (32%), and thoracic aorta (20%). In 106 patients (57%) with serial imaging, new arterial lesions were noted in 41 patients (39%), all of whom had a baseline abnormality, over a mean (±SD) follow-up of 4.39 (2.22) years. New abnormalities were observed in 33% patients by year 2; clinical features of active disease were present at only 50% of these cases. There were no differences in age, sex, temporal artery biopsy positivity, or disease activity in patients with or without new lesions.

Conclusions

In this cohort of patients with GCA, LV abnormalities on first imaging were common. Development of new arterial lesions occurred in patients with arterial abnormalities at first imaging, often in the absence of symptoms of active disease. Arterial imaging should be considered in all patients with GCA at diagnosis and serial imaging at least in patients with baseline abnormalities.
Keywords:ACR  American College of Rheumatology  CTA  computed tomography angiography  ESR  erythrocyte sedimentation rate  GCA  giant cell arteritis  LV  large-vessel  MRA  magnetic resonance angiography  Giant cell arteritis  Computed tomography angiography  Magnetic resonance angiography  Large-artery stenosis  Aortic aneurysm  Disease activity
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