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Updated: Jun 13, 2025

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Aortic and Carotid Complications in Patients With Giant Cell Arteritis
J Anthony Chacko1, Muhammad Z Chauhan1, Paul H Phillips1
1From the Jones Eye Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA (J.A.C., M.Z.C., P.H.P., J.G.C.).
Purpose:
To assess the risk of developing aortic aneurysms (AAs) and carotid artery stenosis (CAS) in patients with giant cell arteritis (GCA), particularly among those presenting with and without visual symptoms.
Design:
Retrospective cohort study.
Subjects:
A total of 7294 patients aged ≥50 years with biopsy-proven GCA (temporal artery biopsy within 2 weeks of diagnosis and ≥3 prednisone refills) were identified and compared with 265 948 control patients presenting with tension-type headache using the TriNetX US Collaborative Network. A secondary comparison was performed between patients with GCA with (n = 2390) and without (n = 5222) visual symptoms (eg, diplopia, amaurosis fugax, vision loss).
Methods:
GCA was defined using International Classification of Diseases, 10th Revision codes M31.5 and M31.6. Patients with a history of other vasculitides, prior AAs, or major thrombotic events were excluded. Propensity score matching was used to balance demographics, socioeconomic factors, comorbidities, substance use, and laboratory/vital parameters, resulting in matched cohorts for each comparison. Adjusted hazard ratios (aHRs) and 95% CIs were estimated using Cox proportional hazards models to account for time to onset of vascular complications.
Main Outcome Measures:
Primary outcomes were the 5-year risks of (1) thoracic AAs, (2) thoracoabdominal AAs, (3) abdominal AAs, and (4) CAS.
Results:
After matching, 7252 patients remained in each arm for the primary GCA versus control comparison. Patients with GCA had a significantly higher 5-year risk of any AA (3.59% vs 1.75%; aHR, 1.98; 95% CI, 1.59-2.45), including thoracic (2.23% vs 1.02%; aHR, 2.01; 95% CI, 1.59-2.77), thoracoabdominal (0.32% vs 0.14%; aHR, 3.68; 95% CI, 1.50-9.05), and abdominal (1.80% vs 0.82%; aHR, 2.03; 95% CI, 1.49-2.77). CAS was also elevated in GCA (7.20% vs 4.37%; aHR, 1.59; 95% CI, 1.38-1.84). In the subanalysis of patients with GCA, the 5-year risk of any AA was comparable between those with and without visual symptoms (3.58% vs 3.23%; aHR, 1.14; 95% CI, 0.83-1.57). However, CAS occurred more frequently in patients with GCA presenting with visual symptoms (8.95% vs 7.43%; aHR, 1.24; 95% CI, 1.01-1.53).
Conclusions:
Patients with GCA demonstrate a substantially increased risk of AAs, particularly thoracic AAs, compared with matched controls. Although having visual symptoms did not correlate with additional aortic risk, they were associated with a higher risk of CAS.
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