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.
Abstract

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