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Open AccessJournal ArticleDOI

Elevated levels of circulating DNA and chromatin are independently associated with severe coronary atherosclerosis and a prothrombotic state.

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TLDR
Evidence is provided demonstrating that markers of cell death and neutrophil extracellular trap formation are independently associated with coronary artery disease, prothrombotic state, and occurrence of adverse cardiac events.
Abstract
Objective—Aberrant neutrophil activation occurs during the advanced stages of atherosclerosis. Once primed, neutrophils can undergo apoptosis or release neutrophil extracellular traps. This extracellular DNA exerts potent proinflammatory, prothrombotic, and cytotoxic properties. The goal of this study was to examine the relationships among extracellular DNA formation, coronary atherosclerosis, and the presence of a prothrombotic state. Approach and Results—In a prospective, observational, cross-sectional cohort of 282 individuals with suspected coronary artery disease, we examined the severity, extent, and phenotype of coronary atherosclerosis using coronary computed tomographic angiography. Double-stranded DNA, nucleosomes, citrullinated histone H4, and myeloperoxidase–DNA complexes, considered in vivo markers of cell death and NETosis, respectively, were established. We further measured various plasma markers of coagulation activation and inflammation. Plasma double-stranded DNA, nucleosomes, and myeloperoxidase–DNA complexes were positively associated with thrombin generation and significantly elevated in patients with severe coronary atherosclerosis or extremely calcified coronary arteries. Multinomial regression analysis, adjusted for confounding factors, identified high plasma nucleosome levels as an independent risk factor of severe coronary stenosis (odds ratio, 2.14; 95% confidence interval, 1.26–3.63; P=0.005). Markers of neutrophil extracellular traps, such as myeloperoxidase–DNA complexes, predicted the number of atherosclerotic coronary vessels and the occurrence of major adverse cardiac events. Conclusions—Our report provides evidence demonstrating that markers of cell death and neutrophil extracellular trap formation are independently associated with coronary artery disease, prothrombotic state, and occurrence of adverse cardiac events. These biomarkers could potentially aid in the prediction of cardiovascular risk in patients with chest discomfort. (Arterioscler Thromb Vasc Biol. 2013;33:2032-2040.)

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Thrombosis: tangled up in NETs.

TL;DR: The biological process of NET formation and how the extracellular release of DNA and protein components of NETs, such as histones and serine proteases, contributes to coagulation and platelet aggregation are described.
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COVID-19 and multisystem inflammatory syndrome in children and adolescents.

TL;DR: In this paper, the authors reviewed the epidemiology, causes, clinical features, and current treatment protocols for multisystem inflammatory syndrome in children and adolescents associated with COVID-19.
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NLRP3 Inflammasome and the IL-1 Pathway in Atherosclerosis.

TL;DR: The mechanisms of NLRP3 inflammasome activation and proinflammatory IL-1 family cytokine production in the context of atherosclerosis are reviewed and treatment possibilities are discussed in light of the positive outcomes of the CANTOS trial.
References
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Journal ArticleDOI

Circulating Nucleosomes and Neutrophil Activation as Risk Factors for Deep Vein Thrombosis

TL;DR: The risk of deep vein thrombosis in humans is increased with higher nucleosome and elastase–&agr;1-antitrypsin complex levels, suggesting a dose-dependent relationship among circulating nucleosomes, activated neutrophils, and DVT.
Journal ArticleDOI

Additive value of semiautomated quantification of coronary artery disease using cardiac computed tomographic angiography to predict future acute coronary syndrome.

TL;DR: The semiautomated plaque quantification algorithm identified several parameters predictive for ACS and provided incremental prognostic value over clinical risk profile and conventional CT reading and the application of this tool may improve risk stratification in patients undergoing CCTA.
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The present state of coronary computed tomography angiography a process in evolution.

TL;DR: The latest available published evidence supporting the potential clinical and cost efficiency of CCTA is described, drawing attention not only to the significance but also the limitations of such studies.
Journal ArticleDOI

The effect of leukocyte elastase on tissue factor pathway inhibitor

TL;DR: Kinetic analysis suggests that HLE cleavage does not effect the affinity of the initial encounter interaction between factor Xa and TFPI, whereas it markedly reduces the affinityOf the final factor XA:TFPI complex with Ki (final) values for untreated and HLE-treated TFPi of 58 pmol/L and 4.4 nmol/ L, respectively.
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