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Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation

INTRODUCTION: Breathing produces a phenomenon of cyclic deformation throughout life. Biomechanically, deformation of the lung is measured as strain. Regional strain recently started to be recognised as a tool in the study of lung pathophysiology, but regional lung strain has not been studied in heal...

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Autores principales: Cruces, Pablo, Erranz, Benjamin, Lillo, Felipe, Sarabia-Vallejos, Mauricio A, Iturrieta, Pablo, Morales, Felipe, Blaha, Katherine, Medina, Tania, Diaz, Franco, Hurtado, Daniel E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830454/
https://www.ncbi.nlm.nih.gov/pubmed/31749967
http://dx.doi.org/10.1136/bmjresp-2019-000423
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author Cruces, Pablo
Erranz, Benjamin
Lillo, Felipe
Sarabia-Vallejos, Mauricio A
Iturrieta, Pablo
Morales, Felipe
Blaha, Katherine
Medina, Tania
Diaz, Franco
Hurtado, Daniel E
author_facet Cruces, Pablo
Erranz, Benjamin
Lillo, Felipe
Sarabia-Vallejos, Mauricio A
Iturrieta, Pablo
Morales, Felipe
Blaha, Katherine
Medina, Tania
Diaz, Franco
Hurtado, Daniel E
author_sort Cruces, Pablo
collection PubMed
description INTRODUCTION: Breathing produces a phenomenon of cyclic deformation throughout life. Biomechanically, deformation of the lung is measured as strain. Regional strain recently started to be recognised as a tool in the study of lung pathophysiology, but regional lung strain has not been studied in healthy subjects breathing spontaneously without voluntary or pharmacological control of ventilation. Our aim is to generate three-dimensional (3D) regional strain and heterogeneity maps of healthy rat lungs and describe their changes over time. METHODS: Micro-CT and image-based biomechanical analysis by finite element approach were carried out in six anaesthetised rats under spontaneous breathing in two different states, at the beginning of the experiment and after 3 hours of observation. 3D regional strain maps were constructed and divided into 10 isovolumetric region-of-interest (ROI) in three directions (apex to base, dorsal to ventral and costal to mediastinal), allowing to regionally analyse the volumetric strain, the strain progression and the strain heterogeneity. To describe in depth these parameters, and systematise their report, we defined regional strain heterogeneity index [1+strain SD ROI(x)]/[1+strain mean ROI(x)] and regional strain progression index [ROI(x)−mean of final strain/ROI(x)−mean of initial strain]. RESULTS: We were able to generate 3D regional strain maps of the lung in subjects without respiratory support, showing significant differences among the three analysed axes. We observed a significantly lower regional volumetric strain in the apex sector compared with the base, with no significant anatomical systematic differences in the other directions. This heterogeneity could not be identified with physiological or standard CT methods. There was no progression of the analysed regional volumetric strain when the two time-points were compared. DISCUSSION: It is possible to map the regional volumetric strain in the lung for healthy subjects during spontaneous breathing. Regional strain heterogeneity and changes over time can be measured using a CT image-based numerical analysis applying a finite element approach. These results support that healthy lung might have significant regional strain and its spatial distribution is highly heterogeneous. This protocol for CT image acquisition and analysis could be a useful tool for helping to understand the mechanobiology of the lung in many diseases.
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spelling pubmed-68304542019-11-20 Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation Cruces, Pablo Erranz, Benjamin Lillo, Felipe Sarabia-Vallejos, Mauricio A Iturrieta, Pablo Morales, Felipe Blaha, Katherine Medina, Tania Diaz, Franco Hurtado, Daniel E BMJ Open Respir Res Respiratory Physiology INTRODUCTION: Breathing produces a phenomenon of cyclic deformation throughout life. Biomechanically, deformation of the lung is measured as strain. Regional strain recently started to be recognised as a tool in the study of lung pathophysiology, but regional lung strain has not been studied in healthy subjects breathing spontaneously without voluntary or pharmacological control of ventilation. Our aim is to generate three-dimensional (3D) regional strain and heterogeneity maps of healthy rat lungs and describe their changes over time. METHODS: Micro-CT and image-based biomechanical analysis by finite element approach were carried out in six anaesthetised rats under spontaneous breathing in two different states, at the beginning of the experiment and after 3 hours of observation. 3D regional strain maps were constructed and divided into 10 isovolumetric region-of-interest (ROI) in three directions (apex to base, dorsal to ventral and costal to mediastinal), allowing to regionally analyse the volumetric strain, the strain progression and the strain heterogeneity. To describe in depth these parameters, and systematise their report, we defined regional strain heterogeneity index [1+strain SD ROI(x)]/[1+strain mean ROI(x)] and regional strain progression index [ROI(x)−mean of final strain/ROI(x)−mean of initial strain]. RESULTS: We were able to generate 3D regional strain maps of the lung in subjects without respiratory support, showing significant differences among the three analysed axes. We observed a significantly lower regional volumetric strain in the apex sector compared with the base, with no significant anatomical systematic differences in the other directions. This heterogeneity could not be identified with physiological or standard CT methods. There was no progression of the analysed regional volumetric strain when the two time-points were compared. DISCUSSION: It is possible to map the regional volumetric strain in the lung for healthy subjects during spontaneous breathing. Regional strain heterogeneity and changes over time can be measured using a CT image-based numerical analysis applying a finite element approach. These results support that healthy lung might have significant regional strain and its spatial distribution is highly heterogeneous. This protocol for CT image acquisition and analysis could be a useful tool for helping to understand the mechanobiology of the lung in many diseases. BMJ Publishing Group 2019-10-28 /pmc/articles/PMC6830454/ /pubmed/31749967 http://dx.doi.org/10.1136/bmjresp-2019-000423 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Respiratory Physiology
Cruces, Pablo
Erranz, Benjamin
Lillo, Felipe
Sarabia-Vallejos, Mauricio A
Iturrieta, Pablo
Morales, Felipe
Blaha, Katherine
Medina, Tania
Diaz, Franco
Hurtado, Daniel E
Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
title Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
title_full Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
title_fullStr Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
title_full_unstemmed Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
title_short Mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
title_sort mapping regional strain in anesthetised healthy subjects during spontaneous ventilation
topic Respiratory Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830454/
https://www.ncbi.nlm.nih.gov/pubmed/31749967
http://dx.doi.org/10.1136/bmjresp-2019-000423
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