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Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns

Most extremely preterm newborns exhibit cerebral atrophy/growth disturbances and white matter signal abnormalities on MRI at term-equivalent age. MRI brain volumes could serve as biomarkers for evaluating the effects of neonatal intensive care and predicting neurodevelopmental outcomes. This require...

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Autores principales: Yu, Xintian, Zhang, Yanjie, Lasky, Robert E., Datta, Sushmita, Parikh, Nehal A., Narayana, Ponnada A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975631/
https://www.ncbi.nlm.nih.gov/pubmed/21079730
http://dx.doi.org/10.1371/journal.pone.0013874
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author Yu, Xintian
Zhang, Yanjie
Lasky, Robert E.
Datta, Sushmita
Parikh, Nehal A.
Narayana, Ponnada A.
author_facet Yu, Xintian
Zhang, Yanjie
Lasky, Robert E.
Datta, Sushmita
Parikh, Nehal A.
Narayana, Ponnada A.
author_sort Yu, Xintian
collection PubMed
description Most extremely preterm newborns exhibit cerebral atrophy/growth disturbances and white matter signal abnormalities on MRI at term-equivalent age. MRI brain volumes could serve as biomarkers for evaluating the effects of neonatal intensive care and predicting neurodevelopmental outcomes. This requires detailed, accurate, and reliable brain MRI segmentation methods. We describe our efforts to develop such methods in high risk newborns using a combination of manual and automated segmentation tools. After intensive efforts to accurately define structural boundaries, two trained raters independently performed manual segmentation of nine subcortical structures using axial T2-weighted MRI scans from 20 randomly selected extremely preterm infants. All scans were re-segmented by both raters to assess reliability. High intra-rater reliability was achieved, as assessed by repeatability and intra-class correlation coefficients (ICC range: 0.97 to 0.99) for all manually segmented regions. Inter-rater reliability was slightly lower (ICC range: 0.93 to 0.99). A semi-automated segmentation approach was developed that combined the parametric strengths of the Hidden Markov Random Field Expectation Maximization algorithm with non-parametric Parzen window classifier resulting in accurate white matter, gray matter, and CSF segmentation. Final manual correction of misclassification errors improved accuracy (similarity index range: 0.87 to 0.89) and facilitated objective quantification of white matter signal abnormalities. The semi-automated and manual methods were seamlessly integrated to generate full brain segmentation within two hours. This comprehensive approach can facilitate the evaluation of large cohorts to rigorously evaluate the utility of regional brain volumes as biomarkers of neonatal care and surrogate endpoints for neurodevelopmental outcomes.
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spelling pubmed-29756312010-11-15 Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns Yu, Xintian Zhang, Yanjie Lasky, Robert E. Datta, Sushmita Parikh, Nehal A. Narayana, Ponnada A. PLoS One Research Article Most extremely preterm newborns exhibit cerebral atrophy/growth disturbances and white matter signal abnormalities on MRI at term-equivalent age. MRI brain volumes could serve as biomarkers for evaluating the effects of neonatal intensive care and predicting neurodevelopmental outcomes. This requires detailed, accurate, and reliable brain MRI segmentation methods. We describe our efforts to develop such methods in high risk newborns using a combination of manual and automated segmentation tools. After intensive efforts to accurately define structural boundaries, two trained raters independently performed manual segmentation of nine subcortical structures using axial T2-weighted MRI scans from 20 randomly selected extremely preterm infants. All scans were re-segmented by both raters to assess reliability. High intra-rater reliability was achieved, as assessed by repeatability and intra-class correlation coefficients (ICC range: 0.97 to 0.99) for all manually segmented regions. Inter-rater reliability was slightly lower (ICC range: 0.93 to 0.99). A semi-automated segmentation approach was developed that combined the parametric strengths of the Hidden Markov Random Field Expectation Maximization algorithm with non-parametric Parzen window classifier resulting in accurate white matter, gray matter, and CSF segmentation. Final manual correction of misclassification errors improved accuracy (similarity index range: 0.87 to 0.89) and facilitated objective quantification of white matter signal abnormalities. The semi-automated and manual methods were seamlessly integrated to generate full brain segmentation within two hours. This comprehensive approach can facilitate the evaluation of large cohorts to rigorously evaluate the utility of regional brain volumes as biomarkers of neonatal care and surrogate endpoints for neurodevelopmental outcomes. Public Library of Science 2010-11-08 /pmc/articles/PMC2975631/ /pubmed/21079730 http://dx.doi.org/10.1371/journal.pone.0013874 Text en Yu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yu, Xintian
Zhang, Yanjie
Lasky, Robert E.
Datta, Sushmita
Parikh, Nehal A.
Narayana, Ponnada A.
Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns
title Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns
title_full Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns
title_fullStr Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns
title_full_unstemmed Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns
title_short Comprehensive Brain MRI Segmentation in High Risk Preterm Newborns
title_sort comprehensive brain mri segmentation in high risk preterm newborns
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975631/
https://www.ncbi.nlm.nih.gov/pubmed/21079730
http://dx.doi.org/10.1371/journal.pone.0013874
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