4.4 Article

Patients with autoimmune chronic inflammatory diseases present increased biomarkers of thromboinflammation and endothelial dysfunction in the absence of flares and cardiovascular comorbidities

期刊

JOURNAL OF THROMBOSIS AND THROMBOLYSIS
卷 53, 期 1, 页码 10-16

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SPRINGER
DOI: 10.1007/s11239-021-02517-0

关键词

Microvesicles; Autoimmune rheumatic diseases; Endothelial dysfunction; Thromboinflammation

资金

  1. European Union (European Social Fund-ESF) through the Operational Programme Human Resources Development, Education and Lifelong Learning 2014-2020 [MIS 5047870]

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The study found that patients with autoimmune rheumatic diseases have increased levels of endothelial and platelet microvesicles, even in the absence of disease flares and cardiovascular comorbidities. These microvesicles may indicate a potential risk for cardiovascular disease in these patients.
Cardiovascular risk is increased in patients with autoimmune rheumatic diseases. Endothelial, erythrocyte and platelet microvesicles (MVs) are elevated in patients with cardiovascular diseases and represent novel markers of endothelial dysfunction and thromboinflammation. We tested whether their levels are increased in patients with autoimmune rheumatic diseases (ARDs) in the absence of disease flare and cardiovascular comorbidities. Well-controlled patients with rheumatoid arthritis or systemic lupus erythematosus were studied, provided they were free from cardiovascular comorbidities and established cardiovascular disease. We additionally studied (a) a control group consisting of healthy volunteers and (b) a reference group including patients with stable coronary artery disease (CAD). MVs were measured using a standardized flow cytometry protocol. In a population of 74 participants, patients with ARDs (n = 17) presented increased levels of both endothelial (283.3 +/- 195.0/mu L vs 168.5 +/- 54.8/mu L, p = 0.029) and platelet MVs (374.0 +/- 275.3/mu L vs 225.7 +/- 101.1/mu L, p = 0.046) compared to controls (n = 34), whereas erythrocyte MVs did not significantly differ. In addition, patients with ARDs showed similar levels of endothelial MVs compared to CAD patients (n = 23) (283.3 +/- 195.0/mu L vs 297.0 +/- 211.8/mu L, p = 0.846). Platelet MVs were significantly associated with disease duration, and erythrocyte MVs with patients' perceived disease activity. In conclusion, increased levels of endothelial and platelet MVs may be evident in patients with ARDs, even in the absence of disease flares and before the establishment of cardiovascular complications. Levels of endothelial MVs resemble those of patients with profound atherothrombotic profile. The prognostic potential of MVs in terms of cardiovascular disease prevention warrants further investigation in patients with ARDs.

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