Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting

Background: Peripheral artery disease (PAD) patients undergoing infrainguinal angioplasty with stenting suffer high rates of target lesion restenosis and ischemic events. Blood-based prognostic markers in these patients are currently limited. The IL-33/ST2-system is involved in atherothrombosis. Sol...

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Main Authors: Stefan Stojkovic, Svitlana Demyanets, Christoph W. Kopp, Christian Hengstenberg, Johann Wojta, Beate Eichelberger, Simon Panzer, Thomas Gremmel
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2020.605669/full
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author Stefan Stojkovic
Svitlana Demyanets
Christoph W. Kopp
Christian Hengstenberg
Johann Wojta
Johann Wojta
Johann Wojta
Beate Eichelberger
Simon Panzer
Thomas Gremmel
Thomas Gremmel
author_facet Stefan Stojkovic
Svitlana Demyanets
Christoph W. Kopp
Christian Hengstenberg
Johann Wojta
Johann Wojta
Johann Wojta
Beate Eichelberger
Simon Panzer
Thomas Gremmel
Thomas Gremmel
author_sort Stefan Stojkovic
collection DOAJ
description Background: Peripheral artery disease (PAD) patients undergoing infrainguinal angioplasty with stenting suffer high rates of target lesion restenosis and ischemic events. Blood-based prognostic markers in these patients are currently limited. The IL-33/ST2-system is involved in atherothrombosis. Soluble ST2 has been proposed as a biomarker in patients with cardiovascular disease.Aim: To investigate the association of sST2 with platelet activation and monocyte tissue factor (TF) in 316 patients undergoing elective angioplasty and stenting for cardiovascular disease, and its predictive value for ischemic outcomes following infrainguinal angioplasty with stent implantation in 104 PAD patients within this cohort.Methods and Results: Circulating levels of sST2, platelet surface P-selectin, monocyte TF expression as well as soluble P-selectin were determined in 316 consecutive patients on dual antiplatelet therapy following angioplasty and stenting. sST2 was independently associated with soluble P-selectin (B = 6.4, 95% CI 2.0–10.7, p = 0.004) and TF expression (B = 0.56, 95% CI 0.02–1.1, p = 0.041) but not with platelet surface P-selectin (B = 0.1, 95% CI −0.1–0.3, p = 0.307) after adjustment for age, sex, clinical risk factors and inflammatory parameters. During the follow-up of 24 months, the primary endpoint occurred in 41 of 104 PAD patients (39.4%). However, circulating levels of sST2 did not predict the primary endpoint in PAD patients (HR 1.1, 95% CI 0.76–1.71, p = 0.527).Conclusion: sST2 is associated with soluble P-selectin and monocyte TF expression in atherosclerosis but not with ischemic outcomes following infrainguinal angioplasty with stent implantation for PAD.
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spelling doaj.art-7684b9173ad74a409d253cb4067ba5d52022-12-21T23:18:34ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2020-12-01710.3389/fcvm.2020.605669605669Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and StentingStefan Stojkovic0Svitlana Demyanets1Christoph W. Kopp2Christian Hengstenberg3Johann Wojta4Johann Wojta5Johann Wojta6Beate Eichelberger7Simon Panzer8Thomas Gremmel9Thomas Gremmel10Department of Internal Medicine II, Medical University of Vienna, Vienna, AustriaDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, AustriaDepartment of Internal Medicine II, Medical University of Vienna, Vienna, AustriaDepartment of Internal Medicine II, Medical University of Vienna, Vienna, AustriaDepartment of Internal Medicine II, Medical University of Vienna, Vienna, AustriaCore Facilities, Medical University of Vienna, Vienna, AustriaLudwig Boltzmann Institute for Cardiovascular Research, Vienna, AustriaDepartment of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, AustriaDepartment of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, AustriaDepartment of Internal Medicine II, Medical University of Vienna, Vienna, AustriaDepartment of Internal Medicine I, Cardiology and Intensive Care Medicine, Landesklinikum Mistelbach-Gänserndorf, Mistelbach, AustriaBackground: Peripheral artery disease (PAD) patients undergoing infrainguinal angioplasty with stenting suffer high rates of target lesion restenosis and ischemic events. Blood-based prognostic markers in these patients are currently limited. The IL-33/ST2-system is involved in atherothrombosis. Soluble ST2 has been proposed as a biomarker in patients with cardiovascular disease.Aim: To investigate the association of sST2 with platelet activation and monocyte tissue factor (TF) in 316 patients undergoing elective angioplasty and stenting for cardiovascular disease, and its predictive value for ischemic outcomes following infrainguinal angioplasty with stent implantation in 104 PAD patients within this cohort.Methods and Results: Circulating levels of sST2, platelet surface P-selectin, monocyte TF expression as well as soluble P-selectin were determined in 316 consecutive patients on dual antiplatelet therapy following angioplasty and stenting. sST2 was independently associated with soluble P-selectin (B = 6.4, 95% CI 2.0–10.7, p = 0.004) and TF expression (B = 0.56, 95% CI 0.02–1.1, p = 0.041) but not with platelet surface P-selectin (B = 0.1, 95% CI −0.1–0.3, p = 0.307) after adjustment for age, sex, clinical risk factors and inflammatory parameters. During the follow-up of 24 months, the primary endpoint occurred in 41 of 104 PAD patients (39.4%). However, circulating levels of sST2 did not predict the primary endpoint in PAD patients (HR 1.1, 95% CI 0.76–1.71, p = 0.527).Conclusion: sST2 is associated with soluble P-selectin and monocyte TF expression in atherosclerosis but not with ischemic outcomes following infrainguinal angioplasty with stent implantation for PAD.https://www.frontiersin.org/articles/10.3389/fcvm.2020.605669/fullperipheral artery diseasesST2ischemic outcomesplatelet reactivitytissue factor
spellingShingle Stefan Stojkovic
Svitlana Demyanets
Christoph W. Kopp
Christian Hengstenberg
Johann Wojta
Johann Wojta
Johann Wojta
Beate Eichelberger
Simon Panzer
Thomas Gremmel
Thomas Gremmel
Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting
Frontiers in Cardiovascular Medicine
peripheral artery disease
sST2
ischemic outcomes
platelet reactivity
tissue factor
title Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting
title_full Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting
title_fullStr Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting
title_full_unstemmed Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting
title_short Association of Soluble Suppression of Tumorigenesis 2 (sST2) With Platelet Activation, Monocyte Tissue Factor and Ischemic Outcomes Following Angioplasty and Stenting
title_sort association of soluble suppression of tumorigenesis 2 sst2 with platelet activation monocyte tissue factor and ischemic outcomes following angioplasty and stenting
topic peripheral artery disease
sST2
ischemic outcomes
platelet reactivity
tissue factor
url https://www.frontiersin.org/articles/10.3389/fcvm.2020.605669/full
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