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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.
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.
Objectives:
Female sex and anticitrullinated protein antibodies (ACPA) are associated with higher disease activity in rheumatoid arthritis (RA). Since disease-related inflammation is linked to cardiovascular risk, we explored whether sex and ACPA influenced the association between disease activity at study entry and cardiovascular risk in established RA.
Methods:
We evaluated 4008 patients with prevalent RA from an international observational cohort enrolled between 1985 and 2012. Outcomes included major adverse cardiovascular events (MACE: cardiovascular death, myocardial infarction and stroke) and ischaemic cardiovascular events (iCVE: MACE, angina, revascularisation, transient ischaemic attack and peripheral arterial disease). Follow-up accrued from enrolment until the first event or censoring. Multivariable Cox models stratified by centre risk evaluated disease activity, sex, ACPA and their interactions.
Results:
We documented 193 MACE and 299 iCVE. Disease activity and sex were associated with MACE (all p≤0.017) and iCVE (p≤0.005) but ACPA was only associated with MACE (p=0.043). A three-way interaction on MACE (p=0.034) but not iCVE was noted. Among ACPA-negative patients, disease activity was associated with MACE in males (HR 1.57 (95% CI 1.14 to 2.16)) but not females (p-for-interaction=0.022). Among ACPA-positive patients, neither the disease activity x sex interaction (p=0.929), nor main effect of disease activity on MACE (p=0.124) was significant, but male sex was (HR 1.61 (95% CI 1.15 to 2.27)). Among females, neither disease activity x ACPA interaction (p=0.523) nor disease activity (p=0.319) was significant for MACE, but ACPA was (HR 1.57 (95% CI 1.02 to 2.42)).
Conclusions:
The effect of disease activity at enrolment on cardiovascular risk in prevalent RA varies across patient groups with different sex and ACPA characteristics.
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