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Published on: January 28, 2020
Antiphospholipid antibodies in patients with myocardial infarction with and without obstructive coronary arteries
Elisabet Svenungsson1, Jonas Spaak2, Karin Strandberg3
1Department of Medicine, Solna, Division of Rheumatology, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Insights
Antiphospholipid antibodies (aPL) IgG are linked to myocardial infarction (MI) in both obstructive (MICAD) and non-obstructive (MINOCA) coronary artery disease. These antibodies, particularly in MICAD, correlate with hypercoagulability, suggesting a role in clotting disorders.
Area of Science:
- Cardiology
- Immunology
- Hematology
Background:
- Prothrombotic antiphospholipid antibodies (aPL) are linked to myocardial infarction (MI) from coronary artery disease (MICAD).
- It remains unclear if aPL differ between MICAD and MI with nonobstructive coronary arteries (MINOCA).
Purpose of the Study:
- To investigate the association of aPL with MINOCA and MICAD.
- To assess if aPL correlate with hypercoagulability, measured by activated protein C-protein C inhibitor (APC-PCI) complex.
Main Methods:
- Cross-sectional case-control study including 98 MINOCA patients, 99 MICAD patients, and 100 controls.
- Analysis of IgA/G/M autoantibodies against cardiolipin and β2 glycoprotein-I using multiplexed bead technology.
- Quantification of APC-PCI complex levels to assess hypercoagulability.
Main Results:
- Prevalence and titers of IgG aPL (anti-cardiolipin and/or anti-β2 glycoprotein-I) were higher in both MINOCA and MICAD patients compared to controls.
- aPL IgG positivity was more frequent in MICAD (11%) than MINOCA (6%), though not statistically significant.
- Elevated APC-PCI levels were observed in aPL IgG-positive MICAD patients, indicating hypercoagulability.
Conclusions:
- IgG aPL are enriched in both MICAD and MINOCA patients compared to controls, with a particular enrichment in MICAD.
- Increased APC-PCI levels in aPL IgG-positive MICAD patients suggest a functional link to coagulation system disturbances.
Background:
Recent studies demonstrate that prothrombotic antiphospholipid antibodies (aPL) are overrepresented in patients with myocardial infarction (MI) due to coronary artery disease (MICAD). However, it is not known whether aPL differ between the two subsets of MI: MICAD and MI with nonobstructive coronary arteries (MINOCA).
Objectives:
To determine whether aPL are associated with MINOCA or MICAD, or with hypercoagulability as assessed by activated protein C-protein C inhibitor (APC-PCI) complex.
Methods:
Well-characterized patients with MINOCA (n = 98), age- and gender-matched patients with MICAD (n = 99), and healthy controls (n = 100) were included in a cross-sectional case-control study. Autoantibodies (IgA/G/M) targeting cardiolipin and β2 glycoprotein-I and specific nuclear antigens were analyzed by multiplexed bead technology. The concentration of APC-PCI was determined as a measure of hypercoagulability by an immunofluorometric sandwich assay.
Results:
Both prevalence and titers of aPL of the IgG isotype (anti-cardiolipin and/or anti-β2 glycoprotein-I) were higher in patients with MINOCA and MICAD than in controls. aPL IgG positivity was twice as frequent among patients with MICAD than MINOCA (11% vs. 6%, nonsignificant). We observed no group differences regarding aPL IgA/M or antibodies targeting specific nuclear antigens. Levels of APC-PCI were elevated in aPL IgG-positive compared to aPL IgG-negative MICAD patients.
Conclusions:
aPL IgG, but not IgA/M, are enriched particularly in patients with MICAD but also in patients with MINOCA, as compared to controls. Interestingly, signs of hypercoagulability-measured by increased levels of the APC-PCI complex-were present in aPL IgG-positive MICAD patients, indicating an association with functional disturbances of the coagulation system.
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