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Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study

Ischemic placental disease is a concept that links intrauterine growth retardation (IUGR) and preeclampsia (PE) back to insufficient remodeling of uterine spiral arteries. The rheological consequences of insufficient remodeling of uterine spiral arteries were hypothesized to mediate the considerably...

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Autores principales: Roth, Christian J., Haeussner, Eva, Ruebelmann, Tanja, Koch, Franz v., Schmitz, Christoph, Frank, Hans-Georg, Wall, Wolfgang A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244422/
https://www.ncbi.nlm.nih.gov/pubmed/28102332
http://dx.doi.org/10.1038/srep40771
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author Roth, Christian J.
Haeussner, Eva
Ruebelmann, Tanja
Koch, Franz v.
Schmitz, Christoph
Frank, Hans-Georg
Wall, Wolfgang A.
author_facet Roth, Christian J.
Haeussner, Eva
Ruebelmann, Tanja
Koch, Franz v.
Schmitz, Christoph
Frank, Hans-Georg
Wall, Wolfgang A.
author_sort Roth, Christian J.
collection PubMed
description Ischemic placental disease is a concept that links intrauterine growth retardation (IUGR) and preeclampsia (PE) back to insufficient remodeling of uterine spiral arteries. The rheological consequences of insufficient remodeling of uterine spiral arteries were hypothesized to mediate the considerably later manifestation of obstetric disease. However, the micro-rheology in the intervillous space (IVS) cannot be examined clinically and rheological animal models of the human IVS do not exist. Thus, an in silico approach was implemented to provide in vivo inaccessible data. The morphology of a spiral artery and the inflow region of the IVS were three-dimensionally reconstructed to provide a morphological stage for the simulations. Advanced high-end supercomputing resources were used to provide blood flow simulations at high spatial resolution. Our simulations revealed turbulent blood flow (high-velocity jets and vortices) combined with elevated blood pressure in the IVS and increased wall shear stress at the villous surface in conjunction with insufficient spiral artery remodeling only. Post-hoc histological analysis of uterine veins showed evidence of increased trophoblast shedding in an IUGR placenta. Our data support that rheological alteration in the IVS is a relevant mechanism linking ischemic placental disease to altered structural integrity and function of the placenta.
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spelling pubmed-52444222017-01-23 Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study Roth, Christian J. Haeussner, Eva Ruebelmann, Tanja Koch, Franz v. Schmitz, Christoph Frank, Hans-Georg Wall, Wolfgang A. Sci Rep Article Ischemic placental disease is a concept that links intrauterine growth retardation (IUGR) and preeclampsia (PE) back to insufficient remodeling of uterine spiral arteries. The rheological consequences of insufficient remodeling of uterine spiral arteries were hypothesized to mediate the considerably later manifestation of obstetric disease. However, the micro-rheology in the intervillous space (IVS) cannot be examined clinically and rheological animal models of the human IVS do not exist. Thus, an in silico approach was implemented to provide in vivo inaccessible data. The morphology of a spiral artery and the inflow region of the IVS were three-dimensionally reconstructed to provide a morphological stage for the simulations. Advanced high-end supercomputing resources were used to provide blood flow simulations at high spatial resolution. Our simulations revealed turbulent blood flow (high-velocity jets and vortices) combined with elevated blood pressure in the IVS and increased wall shear stress at the villous surface in conjunction with insufficient spiral artery remodeling only. Post-hoc histological analysis of uterine veins showed evidence of increased trophoblast shedding in an IUGR placenta. Our data support that rheological alteration in the IVS is a relevant mechanism linking ischemic placental disease to altered structural integrity and function of the placenta. Nature Publishing Group 2017-01-19 /pmc/articles/PMC5244422/ /pubmed/28102332 http://dx.doi.org/10.1038/srep40771 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Roth, Christian J.
Haeussner, Eva
Ruebelmann, Tanja
Koch, Franz v.
Schmitz, Christoph
Frank, Hans-Georg
Wall, Wolfgang A.
Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study
title Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study
title_full Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study
title_fullStr Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study
title_full_unstemmed Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study
title_short Dynamic modeling of uteroplacental blood flow in IUGR indicates vortices and elevated pressure in the intervillous space – a pilot study
title_sort dynamic modeling of uteroplacental blood flow in iugr indicates vortices and elevated pressure in the intervillous space – a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244422/
https://www.ncbi.nlm.nih.gov/pubmed/28102332
http://dx.doi.org/10.1038/srep40771
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