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Published on: February 8, 2019
Risk factors for severe cranial ischaemic complications in giant cell arteritis
Alojzija Hočevar1,2, Rok Ješe1, Matija Tomšič1,2
1Department of Rheumatology, University Medical Centre Ljubljana.
Insights
Risk factors for severe cranial ischemic complications (sCIC) in Giant Cell Arteritis (GCA) include increasing age, jaw claudication, and smoking. Higher C-reactive protein (CRP) levels were found to decrease the risk of sCIC.
Area of Science:
- Neurology
- Rheumatology
- Ophthalmology
Background:
- Giant Cell Arteritis (GCA) is a systemic vasculitis that can lead to severe cranial ischemic complications (sCIC), including vision loss and stroke.
- These complications significantly increase morbidity and mortality in GCA patients.
Purpose of the Study:
- To identify the key risk factors associated with the development of sCIC in patients diagnosed with GCA.
- To differentiate predictors for severe vision complications versus ischemic stroke within the GCA cohort.
Main Methods:
- A prospective analysis of 295 GCA patients diagnosed between September 2011 and August 2019.
- Comparison of clinical and laboratory data between patients with and without sCIC, defined as severe vision complications or stroke.
Main Results:
- Of 295 GCA patients, 61 (20.7%) developed sCIC.
- Multivariable analysis revealed that increasing age (OR 1.08), jaw claudication (OR 3.43), and smoking (OR 1.92) were significant predictors of sCIC.
- Higher C-reactive protein (CRP) levels were associated with a decreased risk of sCIC (OR 0.99).
- Age and jaw claudication increased the risk of severe vision complications, while polymyalgia rheumatica, constitutional symptoms, and higher CRP decreased it.
- Atrial fibrillation was the sole independent predictor of ischemic stroke.
Conclusions:
- Increasing age, jaw claudication, and smoking are significant risk factors for sCIC in GCA.
- Elevated CRP levels may confer a protective effect against sCIC in GCA patients.
- Identifying these risk factors can aid in early detection and prevention strategies for GCA complications.
Objectives:
Vision complications and a stroke represent severe cranial ischaemic complications (sCIC) associated with increased morbidity and mortality in GCA. We aimed to determine the risk factors for sCIC in GCA.
Methods:
We analysed the medical records of prospectively enrolled GCA patients diagnosed between September 2011 and August 2019, and compared the clinical and laboratory characteristics of patients with and without sCIC defined as either severe vision complications (diplopia, transient vision loss, permanent partial vision field/acuity defect and permanent visual loss) or stroke.
Results:
During the 96-month observation period, we identified 295 new GCA patients [65.4% female, median (interquartile range) age 74.7 (67.3-80.0) years]. Sixty-one (20.7%) patients developed sCIC (52 isolated severe vision complications, 5 isolated ischaemic strokes and 4 patients with both complications). In a multivariable logistic regression model jaw claudication [odds ratio (OR) 3.43 (95% CI: 1.84, 6.42), P < 0.001], smoking [OR 1.92 (95% CI: 1.01, 3.65), P = 0.046] and increasing age [OR 1.08 (95% CI: 1.04, 1.13), P < 0.001] were significantly associated with sCIC. Higher CRP [OR 0.99 (0.99-1.00), P = 0.011] decreased the risk of sCIC. When considered separately, the odds for severe vision complications increased with age and jaw claudication, and decreased with polymyalgia rheumatica, constitutional symptoms and higher CRP. Atrial fibrillation emerged as the sole independent predictor of ischaemic stroke.
Conclusion:
Increasing age, jaw claudication and smoking predicted sCIC, while higher CRP decreased the risk of sCIC in our GCA cohort.
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