[Latest advances in diagnosis and therapy of giant cell arteritis (Horton's disease)]

Edwin Curraj1, Camillo Ribi1

  • 1Service d'immunologie et allergologie, Centre hospitalier universitaire vaudois et Université de Lausanne, 1011 Lausanne.

Revue Medicale Suisse
|April 3, 2025
PubMed

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.

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