Sex and anticitrullinated protein antibodies modify the relationship between inflammation and cardiovascular risk in

George A Karpouzas1,2, Virginia Pascual-Ramos3, Miguel A Gonzalez-Gay4,5

  • 1Harbor-UCLA Medical Center, Torrance, California, USA gkarpouzas@lundquist.org.

RMD Open
|February 2, 2026
PubMed

Insights

Cardiovascular risk in rheumatoid arthritis (RA) varies by sex and anticitrullinated protein antibodies (ACPA) status. Disease activity impacts risk differently in males and females, particularly those who are ACPA-negative.

Area of Science:

  • Rheumatology
  • Cardiology
  • Immunology

Background:

  • Rheumatoid arthritis (RA) is linked to increased cardiovascular risk due to chronic inflammation.
  • Female sex and anticitrullinated protein antibodies (ACPA) are known to influence RA disease activity.

Purpose of the Study:

  • To investigate how sex and ACPA status modify the association between RA disease activity and cardiovascular risk.
  • To analyze the impact of disease activity at study entry on major adverse cardiovascular events (MACE) and ischaemic cardiovascular events (iCVE).

Main Methods:

  • Evaluation of 4008 patients with prevalent RA from an international observational cohort.
  • Utilized multivariable Cox models to assess associations between disease activity, sex, ACPA, and cardiovascular events (MACE and iCVE).
  • Follow-up data collected from enrollment (1985-2012) until the first event or censoring.

Main Results:

  • Disease activity and sex were associated with both MACE and iCVE. ACPA was associated with MACE.
  • A significant three-way interaction between disease activity, sex, and ACPA on MACE was observed.
  • In ACPA-negative patients, higher disease activity increased MACE risk in males but not females. In ACPA-positive females, ACPA presence, not disease activity, was linked to MACE.

Conclusions:

  • The relationship between RA disease activity and cardiovascular risk is complex and depends on patient characteristics.
  • Sex and ACPA status are critical factors in stratifying cardiovascular risk in rheumatoid arthritis patients.
Abstract

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