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Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance

In idiopathic pulmonary arterial hypertension (PAH), increased pulmonary vascular resistance is associated with structural narrowing of small (resistance) vessels and increased vascular tone. Current information on pulmonary vascular remodeling is mostly limited to averaged increases in wall thickne...

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Autores principales: Rol, Nina, Timmer, Esther M., Faes, Theo J.C., Noordegraaf, Anton Vonk, Grünberg, Katrien, Bogaard, Harm‐Jan, Westerhof, Nico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371554/
https://www.ncbi.nlm.nih.gov/pubmed/28320897
http://dx.doi.org/10.14814/phy2.13159
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author Rol, Nina
Timmer, Esther M.
Faes, Theo J.C.
Noordegraaf, Anton Vonk
Grünberg, Katrien
Bogaard, Harm‐Jan
Westerhof, Nico
author_facet Rol, Nina
Timmer, Esther M.
Faes, Theo J.C.
Noordegraaf, Anton Vonk
Grünberg, Katrien
Bogaard, Harm‐Jan
Westerhof, Nico
author_sort Rol, Nina
collection PubMed
description In idiopathic pulmonary arterial hypertension (PAH), increased pulmonary vascular resistance is associated with structural narrowing of small (resistance) vessels and increased vascular tone. Current information on pulmonary vascular remodeling is mostly limited to averaged increases in wall thickness, but information on number of vessels affected and internal diameter decreases for vessels of different sizes is limited. Our aim was to quantify numbers of affected vessels and their internal diameter decrease for differently sized vessels in PAH in comparison with non‐PAH patients. Internal and external diameters of transversally cut vessels were measured in five control subjects and six PAH patients. Resistance vessels were classified in Strahler orders, internal diameters 13 μm (order 1) to 500 μm (order 8). The number fraction, that is, percentage of affected vessels, and the internal diameter fraction, that is, percentage diameter of normal diameter, were calculated. In PAH, not all resistance vessels are affected. The number fraction is about 30%, that is, 70% of vessels have diameters not different from vessels of control subjects. Within each order, the decrease in diameter of affected vessels is variable with an averaged diameter fraction of 50–70%. Narrowing of resistance vessels is heterogeneous: not all vessels are narrowed, and the decrease in internal diameters, even within a single order, vary largely. This heterogeneous narrowing alone cannot explain the large resistance increase in PAH. We suggest that rarefaction could be an important contributor to the hemodynamic changes.
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spelling pubmed-53715542017-03-30 Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance Rol, Nina Timmer, Esther M. Faes, Theo J.C. Noordegraaf, Anton Vonk Grünberg, Katrien Bogaard, Harm‐Jan Westerhof, Nico Physiol Rep Original Research In idiopathic pulmonary arterial hypertension (PAH), increased pulmonary vascular resistance is associated with structural narrowing of small (resistance) vessels and increased vascular tone. Current information on pulmonary vascular remodeling is mostly limited to averaged increases in wall thickness, but information on number of vessels affected and internal diameter decreases for vessels of different sizes is limited. Our aim was to quantify numbers of affected vessels and their internal diameter decrease for differently sized vessels in PAH in comparison with non‐PAH patients. Internal and external diameters of transversally cut vessels were measured in five control subjects and six PAH patients. Resistance vessels were classified in Strahler orders, internal diameters 13 μm (order 1) to 500 μm (order 8). The number fraction, that is, percentage of affected vessels, and the internal diameter fraction, that is, percentage diameter of normal diameter, were calculated. In PAH, not all resistance vessels are affected. The number fraction is about 30%, that is, 70% of vessels have diameters not different from vessels of control subjects. Within each order, the decrease in diameter of affected vessels is variable with an averaged diameter fraction of 50–70%. Narrowing of resistance vessels is heterogeneous: not all vessels are narrowed, and the decrease in internal diameters, even within a single order, vary largely. This heterogeneous narrowing alone cannot explain the large resistance increase in PAH. We suggest that rarefaction could be an important contributor to the hemodynamic changes. John Wiley and Sons Inc. 2017-03-21 /pmc/articles/PMC5371554/ /pubmed/28320897 http://dx.doi.org/10.14814/phy2.13159 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Rol, Nina
Timmer, Esther M.
Faes, Theo J.C.
Noordegraaf, Anton Vonk
Grünberg, Katrien
Bogaard, Harm‐Jan
Westerhof, Nico
Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
title Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
title_full Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
title_fullStr Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
title_full_unstemmed Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
title_short Vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
title_sort vascular narrowing in pulmonary arterial hypertension is heterogeneous: rethinking resistance
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371554/
https://www.ncbi.nlm.nih.gov/pubmed/28320897
http://dx.doi.org/10.14814/phy2.13159
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