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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
Aortic aneurysm and dissection in patients with biopsy-proven giant cell arteritis from northwestern Spain: a
Miguel A Gonzalez-Gay1, Carlos Garcia-Porrua, Angela Piñeiro
1From Divisions of Rheumatology (MAG-G, CG-P, AP) and Neurology (RP-R), Hospital Xeral-Calde, Lugo, Spain; Division of Preventive Medicine and Public Health (JL), School of Medicine, University of Cantabria, Santander, Spain; and Division of Rheumatology (GGH), Mayo Clinic, Rochester, Minnesota, United States.
Insights
Giant cell arteritis (GCA) patients with hypertension and severe inflammation face higher risks of aortic aneurysms. Early monitoring is crucial for these GCA individuals to detect aortic disease.
Area of Science:
- Rheumatology
- Cardiovascular Medicine
- Vascular Surgery
Background:
- Giant cell arteritis (GCA) classically presents with occlusive vascular disease.
- Aortic aneurysmal complications in GCA are less frequently documented than ischemic events.
Purpose of the Study:
- To determine the incidence and predictors of aortic aneurysm and dissection in biopsy-proven GCA patients.
- To compare aortic disease incidence in GCA patients from Lugo, Spain, with Olmsted County, MN data.
Main Methods:
- Retrospective analysis of biopsy-proven GCA patients diagnosed between 1981-2001.
- Inclusion of patients from a well-defined population of 250,000.
- Comparison with a 2003 Olmsted County GCA cohort.
Main Results:
- Aortic aneurysmal disease developed in 9.5% (20/210) of GCA patients.
- Incidence of aortic aneurysm/dissection was similar between Lugo (18.9/1000 person-years) and Olmsted County (18.7/1000 person-years).
- Hypertension (HR 4.73) and polymyalgia rheumatica with significant inflammation (HR 3.71) were key predictors.
Conclusions:
- Hypertension and a pronounced inflammatory response at GCA diagnosis are associated with increased aortic aneurysmal disease risk.
- GCA patients exhibiting these risk factors require vigilant monitoring for aortic aneurysm and dissection.
Abstract:
Most classical manifestations of giant cell arteritis (GCA) are the result of occlusive vascular involvement. However, unlike ischemic manifestations, aortic aneurysmal disease in patients with GCA has been less well described. We assessed the incidence and predictors of aortic aneurysm and dissection in patients with biopsy-proven GCA from the Lugo region of northwestern Spain and compared the results with those in a 2003 report from Olmsted County, MN. We performed a retrospective study of biopsy-proven GCA patients diagnosed from 1981 to 2001 at the single hospital for a well-defined population of almost 250,000 people. Twenty (9.5%) of the 210 biopsy-proven GCA patients diagnosed during the study period developed aortic aneurysmal disease. Sixteen of the 20 patients had thoracic aneurysms and 6 had abdominal aneurysms. The incidence of aortic aneurysm and/or dissection in Lugo (18.9 per 1000 person years at risk) was similar to that reported in Olmsted County (18.7 per 1000 person years at risk). Hypertension (hazard ratio: 4.73) and polymyalgia rheumatica with a marked acute inflammatory response at the time of diagnosis of GCA (hazard ratio: 3.71) were the best predictors of aortic aneurysmal disease. Our present observations suggest that a severe inflammatory response associated with hypertension at the time of diagnosis of GCA may promote the development of aortic aneurysmal disease. GCA patients having these features should be monitored for the existence of aortic aneurysm and dissection.
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