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Anti-cardiolipin antibodies and endothelial function in patients with coronary artery disease
Ibrahim Marai1, Michael Shechter, Pnina Langevitz
1Heart Institute, Sheba Medical Center, Tel Hashomer, Israel.
Insights
Cardiovascular disease patients exhibit endothelial dysfunction and higher anticardiolipin antibodies (aCL). This suggests a link between aCL and atherosclerosis, impacting vascular health.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Vascular Biology
Background:
- Endothelial dysfunction is a key indicator and prognostic marker in atherosclerosis.
- Antiphospholipid antibodies (aPL) are prothrombotic and increasingly linked to atherosclerosis development.
Purpose of the Study:
- To investigate the association between endothelial dysfunction and various antiphospholipid autoantibodies.
- To compare these markers in patients with cardiovascular disease (CVD) and healthy controls.
Main Methods:
- Prospective, single-center study involving 107 subjects (45 patients with CVD, 62 healthy controls).
- Assessed endothelial function via flow-mediated dilatation (FMD) and smooth muscle function via nitroglycerin-mediated vasodilatation (NMD).
- Measured autoantibodies including anticardiolipin (aCL; IgG, IgM, IgA), antinuclear antibody, anti-beta2-glycoprotein I (IgG, IgM, IgA), and oxidized LDL.
Main Results:
- Patients with CVD showed significantly lower FMD compared to healthy controls (p=0.012), indicating endothelial dysfunction.
- NMD was nonsignificantly lower in patients (p=0.084).
- Elevated levels of IgG anticardiolipin (aCL) were found in patients with CVD compared to controls.
Conclusions:
- Patients with cardiovascular disease exhibit endothelial dysfunction.
- Elevated levels of immunoglobulin G anticardiolipin antibodies are associated with cardiovascular disease.
- Findings support previous reports linking aCL to atherosclerosis and highlight its role in endothelial dysfunction.
Abstract:
Endothelial dysfunction is considered an important marker in atherosclerosis, having a prognostic value. Antiphospholipid antibodies are considered prothrombotic and have recently been reported to be associated also with atherosclerosis. This study was conducted to investigate a possible association of endothelial dysfunction with various antiphospholipid autoantibodies in healthy subjects and patients with cardiovascular disease. In a single-center, prospective study, 2 groups were included. The study group included patients with cardiovascular diseases (coronary disease and/or cerebrovascular disease) and healthy subjects without apparent heart disease who were referred to the endothelial function laboratory for the assessment of endothelial function. Flow-mediated dilatation, which indicates endothelial function, and nitroglycerin-mediated vasodilatation, which indicates smooth-muscle function, were measured. The 2 groups were evaluated for autoantibodies, including anticardiolipin (aCL; immunoglobulin G [IgG], immunoglobulin M [IgM], and immunoglobulin A [IgA]), antinuclear antibody, anti-beta2-glycoprotein I (IgG, IgM, and IgA), and oxidized low-density lipoprotein. One hundred seven subjects were included in the study: 45 patients (42%) and 62 healthy controls (58%). Flow-mediated dilatation was significantly lower in patients compared with healthy controls (8.0 +/- 9.5% vs 8.0 +/- 13.5%, p = 0.012). In addition, nitroglycerin-mediated vasodilatation was nonsignificantly lower in patients than in healthy controls (8.0 +/- 13.4% vs 11.0 +/- 16.7%, p = 0.084). The mean levels of anti-beta2-glycoprotein I (IgG, IgM, and IgA), aCL (IgM and IgA), antinuclear antibody, and oxidized low-density lipoprotein were not different between groups. However, the mean level of IgG aCL was significantly higher in patients than in healthy controls. In conclusion, in accordance with previous reports of an association between aCL and atherosclerosis, patients with cardiovascular disease had endothelial dysfunction and elevated levels of aCL.
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