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An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field
Fetal Magnetic Resonance Imaging at low field strengths is emerging as an exciting direction in perinatal health. Clinical low field (0.55T) scanners are beneficial for fetal imaging due to their reduced susceptibility-induced artefacts, increased T2* values, and wider bore (widening access for the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cornell University
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441444/ https://www.ncbi.nlm.nih.gov/pubmed/37608939 |
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author | Payette, Kelly Uus, Alena Verdera, Jordina Aviles Zampieri, Carla Avena Hall, Megan Story, Lisa Deprez, Maria Rutherford, Mary A. Hajnal, Joseph V. Ourselin, Sebastien Tomi-Tricot, Raphael Hutter, Jana |
author_facet | Payette, Kelly Uus, Alena Verdera, Jordina Aviles Zampieri, Carla Avena Hall, Megan Story, Lisa Deprez, Maria Rutherford, Mary A. Hajnal, Joseph V. Ourselin, Sebastien Tomi-Tricot, Raphael Hutter, Jana |
author_sort | Payette, Kelly |
collection | PubMed |
description | Fetal Magnetic Resonance Imaging at low field strengths is emerging as an exciting direction in perinatal health. Clinical low field (0.55T) scanners are beneficial for fetal imaging due to their reduced susceptibility-induced artefacts, increased T2* values, and wider bore (widening access for the increasingly obese pregnant population). However, the lack of standard automated image processing tools such as segmentation and reconstruction hampers wider clinical use. In this study, we introduce a semi-automatic pipeline using quantitative MRI for the fetal body at low field strength resulting in fast and detailed quantitative T2* relaxometry analysis of all major fetal body organs. Multi-echo dynamic sequences of the fetal body were acquired and reconstructed into a single high-resolution volume using deformable slice-to-volume reconstruction, generating both structural and quantitative T2* 3D volumes. A neural network trained using a semi-supervised approach was created to automatically segment these fetal body 3D volumes into ten different organs (resulting in dice values > 0.74 for 8 out of 10 organs). The T2* values revealed a strong relationship with GA in the lungs, liver, and kidney parenchyma (R(2) >0.5). This pipeline was used successfully for a wide range of GAs (17–40 weeks), and is robust to motion artefacts. Low field fetal MRI can be used to perform advanced MRI analysis, and is a viable option for clinical scanning. |
format | Online Article Text |
id | pubmed-10441444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cornell University |
record_format | MEDLINE/PubMed |
spelling | pubmed-104414442023-08-22 An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field Payette, Kelly Uus, Alena Verdera, Jordina Aviles Zampieri, Carla Avena Hall, Megan Story, Lisa Deprez, Maria Rutherford, Mary A. Hajnal, Joseph V. Ourselin, Sebastien Tomi-Tricot, Raphael Hutter, Jana ArXiv Article Fetal Magnetic Resonance Imaging at low field strengths is emerging as an exciting direction in perinatal health. Clinical low field (0.55T) scanners are beneficial for fetal imaging due to their reduced susceptibility-induced artefacts, increased T2* values, and wider bore (widening access for the increasingly obese pregnant population). However, the lack of standard automated image processing tools such as segmentation and reconstruction hampers wider clinical use. In this study, we introduce a semi-automatic pipeline using quantitative MRI for the fetal body at low field strength resulting in fast and detailed quantitative T2* relaxometry analysis of all major fetal body organs. Multi-echo dynamic sequences of the fetal body were acquired and reconstructed into a single high-resolution volume using deformable slice-to-volume reconstruction, generating both structural and quantitative T2* 3D volumes. A neural network trained using a semi-supervised approach was created to automatically segment these fetal body 3D volumes into ten different organs (resulting in dice values > 0.74 for 8 out of 10 organs). The T2* values revealed a strong relationship with GA in the lungs, liver, and kidney parenchyma (R(2) >0.5). This pipeline was used successfully for a wide range of GAs (17–40 weeks), and is robust to motion artefacts. Low field fetal MRI can be used to perform advanced MRI analysis, and is a viable option for clinical scanning. Cornell University 2023-08-09 /pmc/articles/PMC10441444/ /pubmed/37608939 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Payette, Kelly Uus, Alena Verdera, Jordina Aviles Zampieri, Carla Avena Hall, Megan Story, Lisa Deprez, Maria Rutherford, Mary A. Hajnal, Joseph V. Ourselin, Sebastien Tomi-Tricot, Raphael Hutter, Jana An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field |
title | An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field |
title_full | An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field |
title_fullStr | An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field |
title_full_unstemmed | An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field |
title_short | An automated pipeline for quantitative T2* fetal body MRI and segmentation at low field |
title_sort | automated pipeline for quantitative t2* fetal body mri and segmentation at low field |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441444/ https://www.ncbi.nlm.nih.gov/pubmed/37608939 |
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