Impact of Biologics on Cardiovascular Events in Ankylosing Spondylitis: A Meta-Analysis

Huijiao Yin1, Yingying Wang1, Zhongqin Chen1

  • 1Rheumatology and Immunology Department, Changxing People's Hospital, Huzhou, Zhejiang, China.

Insights

Biologic therapy may lower cardiovascular event risk in ankylosing spondylitis (AS) patients, reducing myocardial infarction and ischemic heart disease. Further research is needed for specific drug effects and other event types.

Area of Science:

  • Rheumatology
  • Cardiology
  • Pharmacology

Background:

  • Ankylosing spondylitis (AS) is a chronic inflammatory disease.
  • Cardiovascular events (CEs) are a concern in AS patients.
  • The role of biologic therapies in mitigating CEs in AS is under investigation.

Purpose of the Study:

  • To conduct a meta-analysis evaluating the impact of biologic therapies on the incidence of cardiovascular events (CEs) in patients diagnosed with ankylosing spondylitis (AS).

Main Methods:

  • Comprehensive literature searches were conducted across major databases (Embase, Web of Science, PubMed, Cochrane Library) up to March 28, 2025.
  • Quality assessment of included studies utilized the Newcastle-Ottawa Scale and Cochrane Risk of Bias tool.
  • Data analysis was performed using STATA 15.0.

Main Results:

  • The meta-analysis included 23 studies with 92,623 participants.
  • Biologic therapy was associated with a significantly lower overall risk of CEs (RR=0.61, p=0.003), including myocardial infarction (RR=0.42, p<0.001) and ischemic heart disease (RR=0.09, p<0.001).
  • No significant differences in heart failure risk or CEs with etanercept, ixekizumab, or golimumab were observed.

Conclusions:

  • Biologic use appears to reduce the risk of CEs, particularly ischemic heart disease and myocardial infarction, in AS patients.
  • The findings suggest a potential cardiovascular benefit of biologics in AS management.
  • Further large randomized controlled trials are warranted to investigate specific CE subtypes and individual biologic drug effects.
Abstract

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