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Inflammation in Vein Graft Disease

Bypass surgery is one of the most frequently used strategies to revascularize tissues downstream occlusive atherosclerotic lesions. For venous bypass surgery the great saphenous vein is the most commonly used vessel. Unfortunately, graft efficacy is low due to the development of vascular inflammatio...

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Detalles Bibliográficos
Autores principales: de Vries, Margreet R., Quax, Paul H. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787541/
https://www.ncbi.nlm.nih.gov/pubmed/29417051
http://dx.doi.org/10.3389/fcvm.2018.00003
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author de Vries, Margreet R.
Quax, Paul H. A.
author_facet de Vries, Margreet R.
Quax, Paul H. A.
author_sort de Vries, Margreet R.
collection PubMed
description Bypass surgery is one of the most frequently used strategies to revascularize tissues downstream occlusive atherosclerotic lesions. For venous bypass surgery the great saphenous vein is the most commonly used vessel. Unfortunately, graft efficacy is low due to the development of vascular inflammation, intimal hyperplasia and accelerated atherosclerosis. Moreover, failure of grafts leads to significant adverse outcomes and even mortality. The last couple of decades not much has changed in the treatment of vein graft disease (VGD). However, insight is the cellular and molecular mechanisms of VGD has increased. In this review, we discuss the latest insights on VGD and the role of inflammation in this. We discuss vein graft pathophysiology including hemodynamic changes, the role of vessel wall constitutions and vascular remodeling. We show that profound systemic and local inflammatory responses, including inflammation of the perivascular fat, involve both the innate and adaptive immune system.
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spelling pubmed-57875412018-02-07 Inflammation in Vein Graft Disease de Vries, Margreet R. Quax, Paul H. A. Front Cardiovasc Med Cardiovascular Medicine Bypass surgery is one of the most frequently used strategies to revascularize tissues downstream occlusive atherosclerotic lesions. For venous bypass surgery the great saphenous vein is the most commonly used vessel. Unfortunately, graft efficacy is low due to the development of vascular inflammation, intimal hyperplasia and accelerated atherosclerosis. Moreover, failure of grafts leads to significant adverse outcomes and even mortality. The last couple of decades not much has changed in the treatment of vein graft disease (VGD). However, insight is the cellular and molecular mechanisms of VGD has increased. In this review, we discuss the latest insights on VGD and the role of inflammation in this. We discuss vein graft pathophysiology including hemodynamic changes, the role of vessel wall constitutions and vascular remodeling. We show that profound systemic and local inflammatory responses, including inflammation of the perivascular fat, involve both the innate and adaptive immune system. Frontiers Media S.A. 2018-01-24 /pmc/articles/PMC5787541/ /pubmed/29417051 http://dx.doi.org/10.3389/fcvm.2018.00003 Text en Copyright © 2018 de Vries and Quax. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
de Vries, Margreet R.
Quax, Paul H. A.
Inflammation in Vein Graft Disease
title Inflammation in Vein Graft Disease
title_full Inflammation in Vein Graft Disease
title_fullStr Inflammation in Vein Graft Disease
title_full_unstemmed Inflammation in Vein Graft Disease
title_short Inflammation in Vein Graft Disease
title_sort inflammation in vein graft disease
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787541/
https://www.ncbi.nlm.nih.gov/pubmed/29417051
http://dx.doi.org/10.3389/fcvm.2018.00003
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