Publications by authors named "Matthew Kutyna"

Background: Hypoattenuated leaflet thickening (HALT) is believed to reflect leaflet thrombosis; however, no systematic histological examination of HALT has ever been performed. The aim of this study was to evaluate histological findings of explanted self-expanding transcatheter aortic bioprosthetic valves from clinical trials and to compare microCT findings of suspected HALT with histology findings of valve thrombosis and its characterization over time.

Methods: A total of 123 self-expanding transcatheter aortic valves were collected through autopsy (n=89) or surgical explant (n=34) from 11 CoreValve/Evolut clinical trials.

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  • Polygenic risk scores (PRSs) can enhance predictions of coronary artery disease (CAD) risk, and this study investigates their link to histopathologic features of CAD based on autopsy data from 4327 sudden death cases.
  • The analysis involved 954 participants, revealing that those with the highest PRS quintile exhibited significantly worse atherosclerosis characteristics, such as higher %stenosis and greater calcification rates, even when accounting for traditional risk factors.
  • The study concludes that individuals in the highest PRS quintile are at a markedly increased risk of severe atherosclerosis and CAD-related death, especially in those aged 50 and below.
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  • A study was conducted to evaluate the relationship between polygenic risk scores (PRS) for coronary artery disease (CAD) and the severity of atherosclerosis in subjects who died suddenly.
  • From over 4,300 subjects, 954 cases were analyzed, revealing that those in the highest PRS quintile exhibited more severe atherosclerosis and higher rates of critical plaque features compared to those in the lowest quintile.
  • The findings suggest that higher PRS is linked to increased odds of severe atherosclerosis and CAD-related deaths, particularly in younger individuals, marking a significant advancement in understanding CAD risk factors.
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Endothelial shear stress (ESS) plays a key role in the clinical outcomes in native and stented segments; however, their implications in bypass grafts and especially in a synthetic biorestorative coronary artery bypass graft are yet unclear. This report aims to examine the interplay between ESS and the morphological alterations of a biorestorative coronary bypass graft in an animal model. Computational fluid dynamics (CFD) simulation derived from the fusion of angiography and optical coherence tomography (OCT) imaging was used to reconstruct data on the luminal anatomy of a bioresorbable coronary bypass graft with an endoluminal "flap" identified during OCT acquisition.

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Objective: To assess the feasibility and treatment effect of pulsatile intravascular lithotripsy (PIVL) on calcified lesions in a cadaveric model of peripheral artery disease.

Background: PIVL represents a novel potential approach to intravascular lithotripsy for the treatment of vascular calcification.

Methods: In this preclinical device-feasibility study, technical success, calcium morphology and luminal expansion before and after PIVL treatment were evaluated in surgically isolated, perfused atherosclerotic lower-leg arteries and in perfused whole cadaveric lower legs.

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Major advances have been made in coronary artery stent technology over the last decades. Drug-eluting stents reduced in-stent restenosis and have shown better outcomes compared with bare metal stents, yet some limitations still exist to their use. Because they delay healing of the vessel wall, longer dual antiplatelet therapy is mandatory to mitigate against stent thrombosis and this limitation is most concerning in subjects at high risk for bleeding.

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  • - Recent studies indicate the potential benefits of 1-month dual antiplatelet therapy (DAPT) for patients using drug-eluting stents (DES), focusing on the thromboresistance of different stent types under single antiplatelet therapy (SAPT).
  • - The study compared the thrombogenicity of fluoropolymer-coated everolimus-eluting stent (FP-EES), BioLinx polymer zotarolimus-eluting stent (BL-ZES), and biodegradable polymer everolimus-eluting stent (BP-EES) using swine models and confocal microscopy techniques.
  • - Findings showed that FP-EES had significantly lower platelet and inflammatory cell adhesion than the other stents, suggesting
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  • Sudden cardiac death (SCD) without an explanation is linked to genetic factors, but the relationship between specific genetic variants and unexplained SCD in White and African American adults has not been thoroughly studied before.
  • A study involving 683 participants (413 with sequenced DNA) examined the frequency of pathogenic or likely pathogenic (P/LP) variants in genes related to inherited cardiomyopathies and arrhythmia syndromes among those who died from unexplained SCD.
  • The results revealed that 18.4% of participants carried P/LP variants; predominantly, these were linked to hypertrophic cardiomyopathy, dilated cardiomyopathy, and long QT syndrome, highlighting a significant connection between genetic risk factors and unexpl
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Background: In peripheral artery disease, two different types of calcification are frequently observed, i.e., medial and intimal calcification.

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Background: Cytokine storm-related hypercoagulation may be important in the pathogenesis of stent thrombosis in patients with SARS-CoV-2. Whether stent polymers behave differently under such conditions has never been explored.

Methods: Fluorinated polymer-nanocoated and uncoated COBRA stents (CeloNova), BioLinx-polymer-coated Resolute Onyx stents (Medtronic), and Synergy stents (Boston Scientific), which are abluminally coated with a bioabsorbable polymer, were exposed to human blood from healthy donors which was supplemented with 400 pg/mL IL-6 and 100 pg/mL TNF-α, similar to what is seen in cytokine storm caused by SARS-CoV-2.

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Background: Calcified nodule (CN) has a unique plaque morphology, in which an area of nodular calcification causes disruption of the fibrous cap with overlying luminal thrombus. CN is reported to be the least frequent cause of acute coronary thrombosis, and the pathogenesis of CN has not been well studied.

Objectives: The purpose of this study is to provide a comprehensive morphologic assessment of the CN in addition to providing an evolutionary perspective as to how CN causes acute coronary thrombosis in patients with acute coronary syndromes.

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Background: Short-term dual antiplatelet therapy (DAPT) is a suitable strategy after stent implantation especially in patients at high risk for bleeding. The thromboresistant characteristics and the healing profile permanent polymer stents such as the Resolute Onyx- drug-eluting stent (DES) has never been tested against the current approved stents for short-term DAPT, the polymer free (PF) biolimus-eluting stent (PF-BES) and bare metal stents (BMS) in dedicated preclinical models.

Methods: An ex-vivo porcine arteriovenous shunt and in-vivo flow loop model were used to evaluate thromboresistance.

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Objective: To co-register conventional computed tomography angiography (CTA), with ex vivo micro-computed tomography (microCT) and histology of popliteal atherosclerotic plaques. Improving the non-invasive imaging capabilities may be valuable to advance patient care with peripheral arterial obstructive disease towards lesion and individual based treatment.

Methods: In this prospective observational study, 12 popliteal arteries from 11 symptomatic patients who had undergone transfemoral amputations for chronic limb threatening ischaemia and who had pre-operative CTA, were analysed ex vivo by microCT and histology.

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  • The study compares the thrombogenicity (tendency to form clots) and albumin binding of various durable polymer drug-eluting stents (DES) using a swine model and laboratory tests.
  • Results indicated that the fluoropolymer everolimus-eluting stent (FP-EES) had significantly lower platelet adherence and inflammatory cell density compared to other stents and bare metal stents (BMS).
  • FP-EES also demonstrated superior albumin retention, leading to the conclusion that different polymers affect stent performance, potentially influencing their effectiveness in short-term antiplatelet therapy.
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Objectives: The objective of this study was to comprehensively evaluate the pathology of acute and chronic femoral stenting in symptomatic atherosclerotic patients and to understand the causes of stent failure (SF) using multimodality imaging including micro-computed tomography.

Background: Although the pathology of coronary stenting has been well studied, the pathology of lower extremity femoral stenting remains poorly understood.

Methods: Twelve stented femoral lesions removed at surgery (n = 10) and at autopsy (n = 2) were obtained from 10 patients (median age 74 years; interquartile range [IQR]: 66 to 82 years) with histories of peripheral artery disease (critical limb ischemia in 7) (7 men and 3 women).

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Aims: Vascular calcification is routinely encountered in percutaneous coronary intervention (PCI) and severe coronary calcification is a known predictor of in-stent restenosis and stent thrombosis. However, the histopathologic mechanisms behind such events have not been systematically described.

Methods And Results: From our registry of 1211 stents, a total of 134 newer-generation drug-eluting stents (DES) (Xience, Resolute-Integrity, PROMUS-Element, and Synergy) with duration of implant ≥30 days were histologically analysed.

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Implantation of drug-eluting stents (DES) is the dominant treatment strategy for patients with symptomatic coronary artery disease. However, the first-generation DES had substantial drawbacks, including delayed healing, local hypersensitivity reactions and neoatherosclerosis, which all led to a steady increase in major adverse cardiovascular events over time. Subsequently, newer-generation DES were introduced with thinner struts, different scaffold designs (to improve deliverability while maintaining radial strength), different durable and biodegradable polymers - and in some cases no polymer (to improve vascular biocompatibility) - and new antiproliferative drug types and doses.

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  • Coronary artery disease is a major health issue that significantly contributes to illness and death, with factors like intraplaque hemorrhage playing a key role in plaque development.
  • The study focuses on establishing a method to assess the permeability of microvessels in fresh human coronary artery samples using the Evans Blue Dye assay, which had not been previously done.
  • The protocol includes steps for perfusion of arteries, sample collection for analysis, and optional use of a mouse model to further investigate vascular permeability in different health conditions.
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Aims: The aim of this study was to investigate the COBRA PzF stent (C-PzF) with respect to thrombogenicity and healing versus conventional drug-eluting stents (DES) in dedicated preclinical models to evaluate their suitability for short-term dual antiplatelet therapy (DAPT).

Methods And Results: To examine acute thrombogenicity, the C-PzF durable polymer drug-eluting stent (DP-DES), and a bioabsorable polymer DES (BP-DES) were compared in a porcine arteriovenous shunt model and in a rabbit model to evaluate endothelial coverage at 14 days. Barrier function at 28 days in the rabbit was assessed in the former stents as well as in a polymer-free DES (PF-BES).

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Objective- Drug-eluting stents eluting canonical mTOR (mammalian target of rapamycin) inhibitors are widely used to treat coronary artery disease but accelerate the development of atherosclerosis within the stent (neoatherosclerosis)-a leading cause of late stent failure. We recently showed that canonical mTOR inhibitors bind FKBP12.6 (12.

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Intake of hemoglobin by the hemoglobin-haptoglobin receptor CD163 leads to a distinct alternative non-foam cell antiinflammatory macrophage phenotype that was previously considered atheroprotective. Here, we reveal an unexpected but important pathogenic role for these macrophages in atherosclerosis. Using human atherosclerotic samples, cultured cells, and a mouse model of advanced atherosclerosis, we investigated the role of intraplaque hemorrhage on macrophage function with respect to angiogenesis, vascular permeability, inflammation, and plaque progression.

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