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Giant Cell Arteritis (GCA)

Also Known As: Temporal arteritis, Cranial arteritis, Horton’s disease
System: Immune System and Heart and Vascular System
Autoantibodies:
  • No specific autoantibody associated with GCA

  • Diagnosis is based on clinical signs and inflammation markers

Primary Organ or Body Part Affected:

Arteries, especially:

  • Temporal arteries

  • Ophthalmic arteries

  • Aorta and its branches (in some cases)

Acceptance as Autoimmune: Confirmed
Giant Cell Arteritis

What is Giant Cell Arteritis (GCA)?

Giant Cell Arteritis (GCA) is a chronic inflammatory autoimmune disease that affects the large and medium-sized arteries, especially those in the head, neck, and upper body. Most commonly, it involves the temporal arteries on the sides of the head.

The inflammation can narrow or block blood flow, leading to symptoms like headache, scalp tenderness, jaw pain, and vision problems. Without treatment, GCA can lead to permanent vision loss or stroke.

What are the signs and symptoms of Giant Cell Arteritis (GCA)?

  • New, persistent headache (especially at the temples)

  • Scalp tenderness (pain when brushing hair)

  • Jaw pain when chewing (jaw claudication)

  • Vision changes, including blurred vision or sudden blindness in one eye

  • Fatigue, fever, or weight loss

  • Muscle aches (especially shoulders and hips, may overlap with polymyalgia rheumatica)

  • Tender or thickened temporal arteries

What are the causes of Giant Cell Arteritis (GCA)?

GCA is an autoimmune vasculitis, meaning the immune system attacks the blood vessels.
The exact cause is unknown, but contributing factors include:

  • Aging (almost exclusively affects adults over 50)

  • Genetics (certain HLA types)

  • Environmental factors, such as infections, may trigger onset

Diagnosis

  • Blood tests:

    • Elevated ESR (erythrocyte sedimentation rate)

    • Elevated CRP (C-reactive protein)

    • Mild anemia

  • Temporal artery biopsy (confirms diagnosis)

  • Ultrasound of the temporal arteries

  • MRI or PET scans for large-vessel involvement

Treatment

  • High-dose corticosteroids (e.g., prednisone) – started immediately to prevent vision loss

  • Tapering over time under close monitoring

  • Tocilizumab (Actemra) – a biologic approved for GCA in some cases

  • Aspirin may be used to reduce stroke risk

  • Bone protection (calcium, vitamin D, bisphosphonates) if on long-term steroids

Prognosis

  • With early treatment, most people recover well and avoid complications

  • Long-term steroid use may lead to side effects like osteoporosis or diabetes

  • Vision loss, if it occurs, is often permanent

  • Relapses are common and require careful monitoring

Prevalence

  • Estimated at 200 per 100,000 people over age 50

  • Most common in older adults, especially women of Northern European descent

  • Rare in people under 50

Citations

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