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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Persistent aortic inflammation in patients with giant cell arteritis
Mahmut S Kaymakci1, Nicholas A Boire2, Melanie C Bois3
1Division of Rheumatology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Insights
Giant cell arteritis (GCA) patients undergoing thoracic aorta surgery often show active inflammation, even years after diagnosis. This chronic aortitis may lead to aortic aneurysm and dissection, increasing mortality risk.
Area of Science:
- Vascular Surgery
- Rheumatology
- Pathology
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis that can affect large arteries, including the aorta.
- Thoracic aorta aneurysm and dissection are serious complications that can occur in patients with GCA.
Purpose of the Study:
- To investigate the clinicopathologic features of patients with GCA who underwent thoracic aorta surgery.
- To determine the prevalence of active aortitis in GCA patients with thoracic aorta pathology.
- To assess the long-term survival outcomes in GCA patients after thoracic aorta surgery.
Main Methods:
- Retrospective review of patients who underwent thoracic aorta surgery between 2000 and 2021 at Mayo Clinic.
- Screening for prior GCA diagnosis using diagnostic codes and electronic text search.
- Pathologic re-evaluation of thoracic aorta tissues and analysis of clinicopathologic features.
Main Results:
- Of 4621 thoracic aorta surgery patients, 49 had a GCA diagnosis.
- Active aortitis was found in 82% of GCA patients (40/49) during surgery, a median of 6 years post-GCA diagnosis.
- GCA patients had a significantly increased standardized mortality ratio (1.55) compared to the general population.
Conclusions:
- Active aortitis persists in the thoracic aorta of most GCA patients, even when in clinical remission.
- Chronic, smoldering inflammation of the aorta is a likely contributor to aneurysm and dissection development in GCA.
- These findings highlight the importance of long-term surveillance for aortic complications in GCA patients.
Objectives:
To investigate the clinicopathologic features of patients with giant cell arteritis (GCA) who had thoracic aorta aneurysm or dissection surgery.
Methods:
Patients who had thoracic aorta surgery between January 1, 2000, and December 31, 2021, at the Mayo Clinic, Rochester, Minnesota, were identified with current procedural terminology (CPT) codes. The identified patients were screened for a prior diagnosis of GCA with diagnostic codes and electronic text search. The available medical records of all the patients of interest were manually reviewed. Thoracic aorta tissues obtained during surgery were re-evaluated in detail by pathologists. The clinicopathologic features of these patients were analyzed. Overall observed survival was compared with lifetable rates from the United States population.
Results:
Of the 4621 patients with a CPT code for thoracic aorta surgery, 49 had a previous diagnosis of GCA. Histopathologic evaluation of the aortic tissue revealed active aortitis in most patients with GCA (40/49, 82%) after a median (IQR) of 6.0 (2.6-10.3) years from GCA diagnosis. All patients were considered in clinical remission at the time of aortic surgery. The overall mortality compared to age and sex-matched general population was significantly increased with a standardized mortality ratio of 1.55 (95% CI, 1.05-2.19).
Conclusion:
Histopathologic evaluation of the thoracic aorta obtained during surgery revealed active aortitis in most patients with GCA despite being considered in clinical remission several years after GCA diagnosis. Chronic, smoldering aortic inflammation likely contributes to the development of aortic aneurysm and dissection in GCA.
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