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Aspirin reduces anticardiolipin antibodies in patients with coronary artery disease
I Ikonomidis1, J Lekakis, G Vamvakou
1Second Cardiology Department, Attikon University Hospital, University of Athens, N Chalkidona, Athens, Greece. ignoik@otenet.gr
Insights
Aspirin treatment significantly reduced anticardiolipin antibody (aCL) levels in patients with chronic coronary artery disease (CAD). This reduction in immunoglobulin (Ig)A and IgG aCL correlated with decreased C-reactive protein (CRP) levels.
Area of Science:
- Cardiology
- Immunology
- Pharmacology
Background:
- Elevated anticardiolipin antibodies (aCL) are linked to adverse outcomes in coronary artery disease (CAD) due to prothrombotic activity.
- Chronic CAD patients exhibit higher immunoglobulin (Ig)A and IgG aCL levels compared to healthy individuals.
Purpose of the Study:
- To investigate the impact of aspirin on aCL levels in patients with chronic CAD.
- To explore the relationship between aspirin, aCL, and C-reactive protein (CRP) in CAD patients.
Main Methods:
- A double-blind, cross-over trial involving 40 chronic CAD patients and 40 controls.
- Patients received 300 mg daily aspirin or placebo for 12-day periods before coronary artery bypass graft surgery.
- Serum levels of IgA, IgG, IgM-aCL, and CRP were measured.
Main Results:
- Patients with CAD had higher IgA and IgG aCL levels than controls.
- Aspirin treatment significantly reduced IgA, IgG aCL, and CRP levels compared to placebo.
- The reduction in IgA and IgG aCL after aspirin was correlated with CRP reduction.
Conclusions:
- Daily aspirin (300 mg) effectively lowers serum IgA and IgG aCL levels in chronic CAD patients.
- This effect occurs in parallel with a reduction in CRP, suggesting a shared pathophysiological mechanism.
- Findings provide an additional explanation for aspirin's benefits in managing chronic CAD.
Background:
Anticardiolipin antibodies (aCL) have been found to be elevated in patients with coronary artery disease (CAD) and have been associated with an adverse outcome owing to their prothrombotic activity. The aim of this study was to investigate the effect of aspirin treatment on aCL levels in patients with chronic CAD.
Materials And Methods:
Forty patients with chronic CAD scheduled for elective coronary artery bypass graft surgery (CABG) and 40 healthy controls participated in the study. Patients were treated with 300 mg of aspirin once daily (o.d.) for the first 12 days and placebo for the following 12 days before CABG in a double-blind, cross-over trial. Immunoglobulin (Ig) G-, IgM-, IgA-aCL and C-reactive protein (CRP) levels were measured in the controls and at the end of each treatment period in the patients with CAD.
Results:
The IgA- and IgG-aCL levels were greater in patients with CAD than in the controls. Compared with the placebo, IgA, IgG subtypes and CRP levels were reduced after aspirin treatment (P = 0.001, P = 0.02, P = 0.04, respectively). The percentage reduction of IgA- and IgG-aCL was related to the percentage reduction of CRP after aspirin (P < 0.05).
Conclusion:
Aspirin treatment with 300 mg o.d. reduced the serum levels of IgA and IgG subtypes in patients with chronic CAD in parallel to a reduction in CRP. These findings offer an additional pathophysiological mechanism of the beneficial effects of aspirin in patients with chronic CAD.
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