Is Giant Cell Arteritis Associated with Increased Risk of Cardiovascular Disease? A Meta-Analysis

Hritvik Jain1, Maryam Shahzad2, Nandan Patel1

  • 1From the Department of Cardiology, All India Institute of Medical Sciences (AIIMS), Jodhpur, India.

PubMed

Insights

Giant cell arteritis (GCA) significantly increases cardiovascular risks. Patients with GCA face higher chances of myocardial infarction, stroke, and peripheral arterial disease, highlighting the need for early risk management.

Area of Science:

  • Rheumatology
  • Cardiology
  • Epidemiology

Background:

  • Giant cell arteritis (GCA) is the predominant vasculitis affecting individuals over 50.
  • The association between GCA and adverse cardiovascular events remains debated, with conflicting evidence in existing literature.

Purpose of the Study:

  • To conduct a meta-analysis investigating the risks of myocardial infarction (MI), stroke, and peripheral arterial disease (PAD) in patients diagnosed with GCA.

Main Methods:

  • A systematic literature search was performed across major databases (PubMed, EMBASE, Google Scholar, SCOPUS, Web of Science) up to November 1, 2024.
  • Data from 10 studies, encompassing 518,402 participants (28,707 with GCA), were analyzed using a random-effects model in RevMan 5.4.
  • Pooled hazard ratios (HR) with 95% confidence intervals (CI) were calculated to assess cardiovascular risks.

Main Results:

  • GCA was significantly associated with an elevated risk of MI (HR, 1.74; 95% CI, 1.34-2.25).
  • A heightened risk of stroke was observed in GCA patients (HR, 1.43; 95% CI, 1.33-1.54).
  • GCA patients demonstrated a substantially increased risk of PAD (HR, 1.98; 95% CI, 1.53-2.57).

Conclusions:

  • This meta-analysis confirms that GCA patients have a significantly higher risk of major adverse cardiovascular events, including MI, stroke, and PAD.
  • Findings underscore the importance of proactive cardiovascular risk assessment and management in individuals with GCA.
  • Further prospective research is recommended to validate these elevated cardiovascular risks and inform clinical practice.