4.7 Article

Antiphospholipid antibodies in patients with myocardial infarction with and without obstructive coronary arteries

期刊

JOURNAL OF INTERNAL MEDICINE
卷 291, 期 3, 页码 327-337

出版社

WILEY
DOI: 10.1111/joim.13409

关键词

antiphospholipid antibodies; arteriosclerosis; cardiovascular risk factors; coagulation; immunology; myocardial infarction

资金

  1. Swedish Research Council [2018-02535]
  2. Swedish Society of Medicine
  3. Ingegerd Johansson Donation [SLS-713911]
  4. King Gustaf V 80th Birthday Fund [FAI-2019-0628]
  5. Swedish Heart-Lung Foundation [20170257, 20160785, 20190535, 20200552]
  6. Stockholm County Council [20200075, FoUI-948042]
  7. Swedish Rheumatism Association [R-840401]
  8. Swedish Research Council [2018-02535] Funding Source: Swedish Research Council

向作者/读者索取更多资源

Recent studies have shown an overrepresentation of prothrombotic antiphospholipid antibodies in patients with myocardial infarction due to coronary artery disease, but their association with MI with nonobstructive coronary arteries remains unclear. This study confirmed the higher levels of aPL IgG in patients with MI due to coronary artery disease, indicating a potential link with hypercoagulability.
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 beta(2)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-beta(2)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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