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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
[Latest advances in diagnosis and therapy of giant cell arteritis (Horton's disease)]
1Service d'immunologie et allergologie, Centre hospitalier universitaire vaudois et Université de Lausanne, 1011 Lausanne.
Insights
Giant cell arteritis (GCA), a condition affecting large arteries in those over 50, is diagnosed using clinical signs, inflammatory markers, and imaging. Treatment relies on corticosteroids, with new therapies aiming to reduce their use.
Area of Science:
- Rheumatology
- Vascular Medicine
Background:
- Giant cell arteritis (GCA), also known as Horton's disease, is a subacute vasculitis impacting large arteries.
- It predominantly affects individuals over 50, with incidence rising with age.
Purpose of the Study:
- To review the latest recommendations for diagnosing and treating GCA.
- To highlight advancements in diagnostic techniques and therapeutic strategies.
Main Methods:
- Review of current literature and clinical guidelines.
- Discussion of diagnostic criteria including clinical presentation, inflammatory markers, imaging, and histology.
- Evaluation of evolving treatment approaches, including corticosteroids and novel therapies.
Main Results:
- Diagnosis relies on a combination of clinical findings, elevated inflammatory markers, and imaging.
- Temporal artery biopsy, the traditional gold standard, is increasingly supplemented by non-invasive imaging like Doppler ultrasound and PET.
- Corticosteroids are the primary treatment, but newer agents are being developed to minimize steroid-related side effects.
Conclusions:
- Accurate diagnosis of GCA involves integrating multiple data points.
- Non-invasive imaging is becoming crucial in GCA diagnosis, complementing or replacing biopsy.
- Current and emerging treatments aim for effective GCA management while reducing corticosteroid burden.
Abstract:
Giant cell arteritis (GCA, Horton's disease) is a subacute vasculitis of large-size arteries. GCA affects individuals above 50 years and its frequency increases with age. The key elements for diagnosis are clinical presentation, elevated inflammatory markers, imaging, and histology. Temporal artery biopsy is the gold standard for confirming GCA, but is gradually being replaced by non-invasive imaging techniques such as Doppler ultrasound and positron emission tomography. While corticosteroids remain the cornerstone of treatment, new therapies are helping to reduce their dosage and duration of use. In this review, the key aspects of diagnosing and treating GCA, based on the latest recommendations are discussed in this article.
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