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Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry
Quantitative magnetic resonance imaging (MRI) investigations of brain anatomy in children and young adults with Down syndrome (DS) are limited, with no diffusion tensor imaging (DTI) studies covering that age range. We used DTI-driven tensor based morphometry (DTBM), a novel technique that extracts...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096514/ https://www.ncbi.nlm.nih.gov/pubmed/32214129 http://dx.doi.org/10.1038/s41598-020-61799-1 |
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author | Lee, Nancy Raitano Nayak, Amritha Irfanoglu, M. Okan Sadeghi, Neda Stoodley, Catherine J. Adeyemi, Elizabeth Clasen, Liv S. Pierpaoli, Carlo |
author_facet | Lee, Nancy Raitano Nayak, Amritha Irfanoglu, M. Okan Sadeghi, Neda Stoodley, Catherine J. Adeyemi, Elizabeth Clasen, Liv S. Pierpaoli, Carlo |
author_sort | Lee, Nancy Raitano |
collection | PubMed |
description | Quantitative magnetic resonance imaging (MRI) investigations of brain anatomy in children and young adults with Down syndrome (DS) are limited, with no diffusion tensor imaging (DTI) studies covering that age range. We used DTI-driven tensor based morphometry (DTBM), a novel technique that extracts morphometric information from diffusion data, to investigate brain anatomy in 15 participants with DS and 15 age- and sex-matched typically developing (TD) controls, ages 6–24 years (mean age ~17 years). DTBM revealed marked hypoplasia of cerebellar afferent systems in DS, including fronto-pontine (middle cerebellar peduncle) and olivo-cerebellar (inferior cerebellar peduncle) connections. Prominent gray matter hypoplasia was observed in medial frontal regions, the inferior olives, and the cerebellum. Very few abnormalities were detected by classical diffusion MRI metrics, such as fractional anisotropy and mean diffusivity. Our results highlight the potential importance of cerebro-cerebellar networks in the clinical manifestations of DS and suggest a role for DTBM in the investigation of other brain disorders involving white matter hypoplasia or atrophy. |
format | Online Article Text |
id | pubmed-7096514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70965142020-03-30 Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry Lee, Nancy Raitano Nayak, Amritha Irfanoglu, M. Okan Sadeghi, Neda Stoodley, Catherine J. Adeyemi, Elizabeth Clasen, Liv S. Pierpaoli, Carlo Sci Rep Article Quantitative magnetic resonance imaging (MRI) investigations of brain anatomy in children and young adults with Down syndrome (DS) are limited, with no diffusion tensor imaging (DTI) studies covering that age range. We used DTI-driven tensor based morphometry (DTBM), a novel technique that extracts morphometric information from diffusion data, to investigate brain anatomy in 15 participants with DS and 15 age- and sex-matched typically developing (TD) controls, ages 6–24 years (mean age ~17 years). DTBM revealed marked hypoplasia of cerebellar afferent systems in DS, including fronto-pontine (middle cerebellar peduncle) and olivo-cerebellar (inferior cerebellar peduncle) connections. Prominent gray matter hypoplasia was observed in medial frontal regions, the inferior olives, and the cerebellum. Very few abnormalities were detected by classical diffusion MRI metrics, such as fractional anisotropy and mean diffusivity. Our results highlight the potential importance of cerebro-cerebellar networks in the clinical manifestations of DS and suggest a role for DTBM in the investigation of other brain disorders involving white matter hypoplasia or atrophy. Nature Publishing Group UK 2020-03-25 /pmc/articles/PMC7096514/ /pubmed/32214129 http://dx.doi.org/10.1038/s41598-020-61799-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Nancy Raitano Nayak, Amritha Irfanoglu, M. Okan Sadeghi, Neda Stoodley, Catherine J. Adeyemi, Elizabeth Clasen, Liv S. Pierpaoli, Carlo Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry |
title | Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry |
title_full | Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry |
title_fullStr | Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry |
title_full_unstemmed | Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry |
title_short | Hypoplasia of cerebellar afferent networks in Down syndrome revealed by DTI-driven tensor based morphometry |
title_sort | hypoplasia of cerebellar afferent networks in down syndrome revealed by dti-driven tensor based morphometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096514/ https://www.ncbi.nlm.nih.gov/pubmed/32214129 http://dx.doi.org/10.1038/s41598-020-61799-1 |
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