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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
Do Early Diagnosis and Glucocorticoid Treatment Decrease the Risk of Permanent Visual Loss and Early Relapses in
Alojzija Hocevar1, Ziga Rotar, Rok Jese
1From the Department of Rheumatology (AH, ZR, RJ, SSS, MT); Department of Ophthalmology (MH); University Medical Centre Ljubljana, Institute of Pathology (JP); Faculty of Medicine (MT), University of Ljubljana, Ljubljana, Slovenia; and Faculty of Mathematics, Natural Science and Information Technology (SSS), University of Primorska, Koper, Slovenia.
Early diagnosis and treatment of giant cell arteritis (GCA) reduced permanent visual loss (PVL). However, GCA relapse rates remain high, predicted by baseline inflammation markers, despite prompt glucocorticoid (GC) therapy.
Area of Science:
- Rheumatology
- Ophthalmology
- Internal Medicine
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis that can lead to severe complications like permanent visual loss (PVL).
- Glucocorticoids (GCs) are the cornerstone of GCA treatment, but their long-term use is associated with significant side effects, and relapses can occur during dose tapering.
Purpose of the Study:
- To determine the incidence of permanent visual loss (PVL) in patients with giant cell arteritis (GCA).
- To assess the GCA relapse rate during glucocorticoid (GC) tapering.
- To identify factors associated with PVL and GCA relapse.
Main Methods:
- A prospective, longitudinal study conducted at a single rheumatology center in Slovenia from September 2011 to September 2014.
- Sixty-eight GCA patients were followed for a median of 104 weeks, with clinical and laboratory assessments at predetermined intervals.
- Patients were categorized into 'early GCA' (symptoms <31 days) and 'late GCA' (symptoms ≥31 days) groups.
Main Results:
- The incidence of PVL was 5.9% (4 out of 68 patients), with only one case in the early GCA group.
- GCA relapse rates were high in both early (43.6%) and late (48.3%) GCA groups.
- Relapses were predicted by significantly higher baseline levels of inflammatory markers (ESR, CRP, serum amyloid A, haptoglobin, fibrinogen).
Conclusions:
- Early GCA diagnosis and prompt GC treatment appear to decrease the PVL rate compared to historical data.
- The frequency of GCA relapses during GC tapering was not significantly impacted by early diagnosis or prompt treatment.
- High baseline inflammatory biomarker levels are predictive of GCA relapses, suggesting a need for closer monitoring in such patients.
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