Skip to content

How old do you have to be to get temporal arteritis? The answer for seniors

Temporal arteritis, also known as giant cell arteritis, is a condition that almost never occurs in adults under the age of 50. The answer to how old do you have to be to get temporal arteritis is therefore critically linked to the senior population, with most diagnoses happening in the 70s.

Quick Summary

Temporal arteritis is a condition that overwhelmingly affects adults over the age of 50, with the peak incidence observed in the seventh and eighth decades of life. It is extremely rare in younger individuals, though some rare exceptions exist.

Key Points

  • Age is the primary risk factor: Temporal arteritis almost exclusively affects adults over 50, with a mean age of onset typically in the 70s.

  • Rapid vision loss risk: The most feared complication is sudden, irreversible blindness, making prompt diagnosis and treatment essential.

  • Distinctive symptoms: Look for new-onset headache, scalp tenderness, jaw pain with chewing (jaw claudication), and vision changes.

  • Polymyalgia Rheumatica link: Many GCA patients also have PMR, which causes muscle pain and stiffness, particularly in the shoulders and hips.

  • Immediate treatment needed: If GCA is suspected, high-dose corticosteroids are started immediately to prevent vision loss; this often happens before biopsy results are confirmed.

  • Rarity in younger individuals: While a rare juvenile form exists, the classic form of GCA is extremely uncommon in people under 50.

In This Article

Understanding the Age Factor in Temporal Arteritis

Temporal arteritis (TA), also referred to as giant cell arteritis (GCA), is a serious inflammatory disease of the arteries. While it can affect various medium and large arteries, it most famously impacts the temporal arteries in the head, hence its name. Age is the most significant and well-documented risk factor for this condition, with the vast majority of cases occurring in people over 50. The incidence of GCA increases steadily with age, peaking between the ages of 70 and 79.

Experts theorize that the connection to aging might be due to age-related changes in the immune system. As the body's immune response changes over time, it may become more prone to attacking its own blood vessels in a misguided inflammatory reaction. This makes GCA fundamentally a disease of the elderly, and healthcare providers use this age cutoff as a key piece of information when considering a diagnosis.

Key Risk Factors Beyond Age

While age is the primary factor, other characteristics can increase a person's risk of developing temporal arteritis:

  • Sex: Women are roughly two to three times more likely to develop GCA than men.
  • Race and Geographic Location: The condition is most common among white populations of Northern European or Scandinavian descent. Incidence is lower in other ethnic groups, including those of African and Asian descent.
  • Polymyalgia Rheumatica (PMR): A person with PMR, another inflammatory condition causing muscle stiffness and pain, has an increased risk of also developing GCA. In fact, between 40% and 60% of people with GCA also have PMR.
  • Family History: A family history of GCA can increase an individual's likelihood of developing the disease, suggesting a potential genetic predisposition.

Recognizing the Symptoms: What to Look For

Many of the symptoms of temporal arteritis are tied to the inflammation and narrowing of arteries, which reduces blood flow to different parts of the body. It is critical for older adults and their caregivers to recognize these signs early, as the most serious complications, particularly vision loss, can occur rapidly.

Common signs of temporal arteritis include:

  • New, Persistent Headaches: Often a severe, throbbing headache located in the temples or forehead, but it can also occur in other areas of the head.
  • Scalp Tenderness: The scalp, especially around the temples, may become sensitive to the touch, making it painful to brush hair or rest one's head.
  • Jaw Claudication: Pain in the jaw muscles that worsens when chewing. This is a tell-tale sign of reduced blood flow to the jaw muscles.
  • Vision Disturbances: This is a medical emergency. Symptoms can include blurred vision, double vision, temporary loss of vision (amaurosis fugax), or sudden, irreversible blindness in one or both eyes.
  • Systemic Symptoms: These can mimic a flu-like illness and include fever, fatigue, weight loss, and general malaise.
  • Polymyalgia Rheumatica Symptoms: If coexisting with PMR, patients may experience pain and stiffness in the neck, shoulders, and hips.

Diagnosing Temporal Arteritis in the Elderly

Diagnosing GCA in older patients typically involves a combination of clinical evaluation, blood tests, and potentially a biopsy. The diagnosis should be considered a priority due to the risk of vision loss.

  1. Clinical Assessment: The doctor will evaluate symptoms, focusing on the five criteria established by the American College of Rheumatology. Age of onset is the first of these criteria.
  2. Blood Tests: Erythrocyte Sedimentation Rate (ESR) and C-Reactive Protein (CRP) are inflammatory markers that are often significantly elevated in GCA.
  3. Temporal Artery Biopsy: This is considered the gold standard for confirming the diagnosis. A small section of the temporal artery is removed and examined for signs of inflammation and the characteristic "giant cells." It is important to note that treatment should be started immediately if GCA is suspected, even before biopsy results are available, to prevent vision loss.
  4. Imaging: Other diagnostic tools, such as vascular ultrasound, can help assess the arteries for inflammation.

Comparing Classical and Juvenile Temporal Arteritis

For clarity, it's helpful to distinguish between the two extremely rare forms of the disease that can affect younger people versus the common form in older adults.

Feature Classic Giant Cell Arteritis (GCA) Juvenile Temporal Arteritis (JTA)
Age at Onset Almost exclusively over 50, with peak incidence in 70s Exceedingly rare, occurs in children and young adults
Systemic Symptoms Common, including fever, fatigue, weight loss Less common; often benign prognosis
Inflammation Systemic, affecting medium and large arteries throughout the body Localized inflammatory lesion, primarily of the temporal arteries
Vision Risk Significant and serious risk of permanent vision loss Rare, usually not associated with systemic complications

Conclusion: Age and Vigilance

For anyone over the age of 50, especially women of Northern European descent, new and persistent symptoms like headaches, scalp tenderness, or jaw pain should prompt a visit to a doctor. The link between age and temporal arteritis is undeniable, and quick action can prevent irreversible complications like vision loss. Early diagnosis and immediate treatment with corticosteroids are the keys to a positive outcome.

To learn more about GCA, you can consult resources such as the Johns Hopkins Vasculitis Center.

Frequently Asked Questions

Temporal arteritis, or giant cell arteritis, is a disease of older adults that almost exclusively affects people over the age of 50. The average age of onset is typically in the 70s.

It is extremely rare for someone under 50 to get classic giant cell arteritis. While a rare, distinct juvenile form exists, it affects the temporal arteries of children and young adults but has a more benign prognosis than classic GCA.

Most people diagnosed with temporal arteritis are between the ages of 70 and 80. The disease's incidence increases significantly with age after 50.

Initial symptoms can include a new or persistent headache, often localized to the temples, fatigue, fever, weight loss, and general malaise.

A patient's age is a critical diagnostic factor, as the disease is highly age-dependent. The American College of Rheumatology criteria for diagnosis specifically include age 50 or older at onset.

Prompt treatment is essential because temporal arteritis can cause sudden, permanent, and irreversible vision loss if not addressed quickly with high-dose corticosteroids.

Yes, there is a strong link between the two conditions. Approximately 40-60% of people with giant cell arteritis also have polymyalgia rheumatica, an inflammatory condition causing muscle pain and stiffness.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice. Always consult a qualified healthcare provider regarding personal health decisions.