Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/119307
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Type: Journal article
Title: Neonatal brain tissue classification with morphological adaptation and unified segmentation
Author: Beare, R.J.
Chen, J.
Kelly, C.E.
Alexopoulos, D.
Smyser, C.D.
Rogers, C.E.
Loh, W.Y.
Matthews, L.G.
Cheong, J.L.Y.
Spittle, A.J.
Anderson, P.J.
Doyle, L.W.
Inder, T.E.
Seal, M.L.
Thompson, D.K.
Citation: Frontiers in Neuroinformatics, 2016; 10(MAR):12-1-12-17
Publisher: Frontiers Media
Issue Date: 2016
ISSN: 1662-5196
1662-5196
Statement of
Responsibility: 
Richard J. Beare, Jian Chen, Claire E. Kelly, Dimitrios Alexopoulos, Christopher D. Smyser, Cynthia E. Rogers, Wai Y. Loh, Lillian G. Matthews, Jeanie L. Y. Cheong, Alicia J. Spittle, Peter J. Anderson, Lex W. Doyle, Terrie E. Inder, Marc L. Seal and Deanne K. Thompson
Abstract: Measuring the distribution of brain tissue types (tissue classification) in neonates is necessary for studying typical and atypical brain development, such as that associated with preterm birth, and may provide biomarkers for neurodevelopmental outcomes. Compared with magnetic resonance images of adults, neonatal images present specific challenges that require the development of specialized, population-specific methods. This paper introduces MANTiS (Morphologically Adaptive Neonatal Tissue Segmentation), which extends the unified segmentation approach to tissue classification implemented in Statistical Parametric Mapping (SPM) software to neonates. MANTiS utilizes a combination of unified segmentation, template adaptation via morphological segmentation tools and topological filtering, to segment the neonatal brain into eight tissue classes: cortical gray matter, white matter, deep nuclear gray matter, cerebellum, brainstem, cerebrospinal fluid (CSF), hippocampus and amygdala. We evaluated the performance of MANTiS using two independent datasets. The first dataset, provided by the NeoBrainS12 challenge, consisted of coronal T2-weighted images of preterm infants (born ≤30 weeks' gestation) acquired at 30 weeks' corrected gestational age (n = 5), coronal T2-weighted images of preterm infants acquired at 40 weeks' corrected gestational age (n = 5) and axial T2-weighted images of preterm infants acquired at 40 weeks' corrected gestational age (n = 5). The second dataset, provided by the Washington University NeuroDevelopmental Research (WUNDeR) group, consisted of T2-weighted images of preterm infants (born <30 weeks' gestation) acquired shortly after birth (n = 12), preterm infants acquired at term-equivalent age (n = 12), and healthy term-born infants (born ≥38 weeks' gestation) acquired within the first 9 days of life (n = 12). For the NeoBrainS12 dataset, mean Dice scores comparing MANTiS with manual segmentations were all above 0.7, except for the cortical gray matter for coronal images acquired at 30 weeks. This demonstrates that MANTiS' performance is competitive with existing techniques. For the WUNDeR dataset, mean Dice scores comparing MANTiS with manually edited segmentations demonstrated good agreement, where all scores were above 0.75, except for the hippocampus and amygdala. The results show that MANTiS is able to segment neonatal brain tissues well, even in images that have brain abnormalities common in preterm infants. MANTiS is available for download as an SPM toolbox from http://developmentalimagingmcri.github.io/mantis.
Keywords: Magnetic resonance imaging; tissue classification; statistical parametric mapping; neonate; preterm birth
Rights: © 2016 Beare, Chen, Kelly, Alexopoulos, Smyser, Rogers, Loh, Matthews, Cheong, Spittle, Anderson, Doyle, Inder, Seal and Thompson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
DOI: 10.3389/fninf.2016.00012
Grant ID: http://purl.org/au-research/grants/nhmrc/1028822
http://purl.org/au-research/grants/nhmrc/546519
http://purl.org/au-research/grants/nhmrc/1060733
http://purl.org/au-research/grants/nhmrc/1081288
http://purl.org/au-research/grants/nhmrc/1053787
http://purl.org/au-research/grants/nhmrc/1053767
http://purl.org/au-research/grants/nhmrc/1012236
Published version: http://dx.doi.org/10.3389/fninf.2016.00012
Appears in Collections:Aurora harvest 4
Dentistry publications

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