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Stresses and strains on the human fetal skeleton during development

Mechanical forces generated by fetal kicks and movements result in stimulation of the fetal skeleton in the form of stress and strain. This stimulation is known to be critical for prenatal musculoskeletal development; indeed, abnormal or absent movements have been implicated in multiple congenital d...

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Autores principales: Verbruggen, Stefaan W., Kainz, Bernhard, Shelmerdine, Susan C., Hajnal, Joseph V., Rutherford, Mary A., Arthurs, Owen J., Phillips, Andrew T. M., Nowlan, Niamh C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805961/
https://www.ncbi.nlm.nih.gov/pubmed/29367236
http://dx.doi.org/10.1098/rsif.2017.0593
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author Verbruggen, Stefaan W.
Kainz, Bernhard
Shelmerdine, Susan C.
Hajnal, Joseph V.
Rutherford, Mary A.
Arthurs, Owen J.
Phillips, Andrew T. M.
Nowlan, Niamh C.
author_facet Verbruggen, Stefaan W.
Kainz, Bernhard
Shelmerdine, Susan C.
Hajnal, Joseph V.
Rutherford, Mary A.
Arthurs, Owen J.
Phillips, Andrew T. M.
Nowlan, Niamh C.
author_sort Verbruggen, Stefaan W.
collection PubMed
description Mechanical forces generated by fetal kicks and movements result in stimulation of the fetal skeleton in the form of stress and strain. This stimulation is known to be critical for prenatal musculoskeletal development; indeed, abnormal or absent movements have been implicated in multiple congenital disorders. However, the mechanical stress and strain experienced by the developing human skeleton in utero have never before been characterized. Here, we quantify the biomechanics of fetal movements during the second half of gestation by modelling fetal movements captured using novel cine-magnetic resonance imaging technology. By tracking these movements, quantifying fetal kick and muscle forces, and applying them to three-dimensional geometries of the fetal skeleton, we test the hypothesis that stress and strain change over ontogeny. We find that fetal kick force increases significantly from 20 to 30 weeks' gestation, before decreasing towards term. However, stress and strain in the fetal skeleton rises significantly over the latter half of gestation. This increasing trend with gestational age is important because changes in fetal movement patterns in late pregnancy have been linked to poor fetal outcomes and musculoskeletal malformations. This research represents the first quantification of kick force and mechanical stress and strain due to fetal movements in the human skeleton in utero, thus advancing our understanding of the biomechanical environment of the uterus. Further, by revealing a potential link between fetal biomechanics and skeletal malformations, our work will stimulate future research in tissue engineering and mechanobiology.
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spelling pubmed-58059612018-02-13 Stresses and strains on the human fetal skeleton during development Verbruggen, Stefaan W. Kainz, Bernhard Shelmerdine, Susan C. Hajnal, Joseph V. Rutherford, Mary A. Arthurs, Owen J. Phillips, Andrew T. M. Nowlan, Niamh C. J R Soc Interface Life Sciences–Engineering interface Mechanical forces generated by fetal kicks and movements result in stimulation of the fetal skeleton in the form of stress and strain. This stimulation is known to be critical for prenatal musculoskeletal development; indeed, abnormal or absent movements have been implicated in multiple congenital disorders. However, the mechanical stress and strain experienced by the developing human skeleton in utero have never before been characterized. Here, we quantify the biomechanics of fetal movements during the second half of gestation by modelling fetal movements captured using novel cine-magnetic resonance imaging technology. By tracking these movements, quantifying fetal kick and muscle forces, and applying them to three-dimensional geometries of the fetal skeleton, we test the hypothesis that stress and strain change over ontogeny. We find that fetal kick force increases significantly from 20 to 30 weeks' gestation, before decreasing towards term. However, stress and strain in the fetal skeleton rises significantly over the latter half of gestation. This increasing trend with gestational age is important because changes in fetal movement patterns in late pregnancy have been linked to poor fetal outcomes and musculoskeletal malformations. This research represents the first quantification of kick force and mechanical stress and strain due to fetal movements in the human skeleton in utero, thus advancing our understanding of the biomechanical environment of the uterus. Further, by revealing a potential link between fetal biomechanics and skeletal malformations, our work will stimulate future research in tissue engineering and mechanobiology. The Royal Society 2018-01 2018-01-24 /pmc/articles/PMC5805961/ /pubmed/29367236 http://dx.doi.org/10.1098/rsif.2017.0593 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Engineering interface
Verbruggen, Stefaan W.
Kainz, Bernhard
Shelmerdine, Susan C.
Hajnal, Joseph V.
Rutherford, Mary A.
Arthurs, Owen J.
Phillips, Andrew T. M.
Nowlan, Niamh C.
Stresses and strains on the human fetal skeleton during development
title Stresses and strains on the human fetal skeleton during development
title_full Stresses and strains on the human fetal skeleton during development
title_fullStr Stresses and strains on the human fetal skeleton during development
title_full_unstemmed Stresses and strains on the human fetal skeleton during development
title_short Stresses and strains on the human fetal skeleton during development
title_sort stresses and strains on the human fetal skeleton during development
topic Life Sciences–Engineering interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805961/
https://www.ncbi.nlm.nih.gov/pubmed/29367236
http://dx.doi.org/10.1098/rsif.2017.0593
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