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Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging
Variant late-infantile Batten disease is a neuronal ceroid lipofuscinosis caused by mutations in CLN6. It is a recessive genetic lysosomal storage disease characterised by progressive neurodegeneration. It starts insidiously and leads to blindness, epilepsy and dementia in affected children. Sheep t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498759/ https://www.ncbi.nlm.nih.gov/pubmed/26161747 http://dx.doi.org/10.1371/journal.pone.0132331 |
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author | Sawiak, Stephen J. Perumal, Sunthara Rajan Rudiger, Skye R. Matthews, Loren Mitchell, Nadia L. McLaughlan, Clive J. Bawden, C. Simon Palmer, David N. Kuchel, Timothy Morton, A. Jennifer |
author_facet | Sawiak, Stephen J. Perumal, Sunthara Rajan Rudiger, Skye R. Matthews, Loren Mitchell, Nadia L. McLaughlan, Clive J. Bawden, C. Simon Palmer, David N. Kuchel, Timothy Morton, A. Jennifer |
author_sort | Sawiak, Stephen J. |
collection | PubMed |
description | Variant late-infantile Batten disease is a neuronal ceroid lipofuscinosis caused by mutations in CLN6. It is a recessive genetic lysosomal storage disease characterised by progressive neurodegeneration. It starts insidiously and leads to blindness, epilepsy and dementia in affected children. Sheep that are homozygous for a natural mutation in CLN6 have an ovine form of Batten disease Here, we used in vivo magnetic resonance imaging to track brain changes in 4 unaffected carriers and 6 affected Batten disease sheep. We scanned each sheep 4 times, between 17 and 22 months of age. Cortical atrophy in all sheep was pronounced at the baseline scan in all affected Batten disease sheep. Significant atrophy was also present in other brain regions (caudate, putamen and amygdala). Atrophy continued measurably in all of these regions during the study. Longitudinal MRI in sheep was sensitive enough to measure significant volume changes over the relatively short study period, even in the cortex, where nearly 40% of volume was already lost at the start of the study. Thus longitudinal MRI could be used to study the dynamics of progression of neurodegenerative changes in sheep models of Batten disease, as well as to assess therapeutic efficacy. |
format | Online Article Text |
id | pubmed-4498759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44987592015-07-17 Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging Sawiak, Stephen J. Perumal, Sunthara Rajan Rudiger, Skye R. Matthews, Loren Mitchell, Nadia L. McLaughlan, Clive J. Bawden, C. Simon Palmer, David N. Kuchel, Timothy Morton, A. Jennifer PLoS One Research Article Variant late-infantile Batten disease is a neuronal ceroid lipofuscinosis caused by mutations in CLN6. It is a recessive genetic lysosomal storage disease characterised by progressive neurodegeneration. It starts insidiously and leads to blindness, epilepsy and dementia in affected children. Sheep that are homozygous for a natural mutation in CLN6 have an ovine form of Batten disease Here, we used in vivo magnetic resonance imaging to track brain changes in 4 unaffected carriers and 6 affected Batten disease sheep. We scanned each sheep 4 times, between 17 and 22 months of age. Cortical atrophy in all sheep was pronounced at the baseline scan in all affected Batten disease sheep. Significant atrophy was also present in other brain regions (caudate, putamen and amygdala). Atrophy continued measurably in all of these regions during the study. Longitudinal MRI in sheep was sensitive enough to measure significant volume changes over the relatively short study period, even in the cortex, where nearly 40% of volume was already lost at the start of the study. Thus longitudinal MRI could be used to study the dynamics of progression of neurodegenerative changes in sheep models of Batten disease, as well as to assess therapeutic efficacy. Public Library of Science 2015-07-10 /pmc/articles/PMC4498759/ /pubmed/26161747 http://dx.doi.org/10.1371/journal.pone.0132331 Text en © 2015 Sawiak 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 Sawiak, Stephen J. Perumal, Sunthara Rajan Rudiger, Skye R. Matthews, Loren Mitchell, Nadia L. McLaughlan, Clive J. Bawden, C. Simon Palmer, David N. Kuchel, Timothy Morton, A. Jennifer Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging |
title | Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging |
title_full | Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging |
title_fullStr | Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging |
title_full_unstemmed | Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging |
title_short | Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging |
title_sort | rapid and progressive regional brain atrophy in cln6 batten disease affected sheep measured with longitudinal magnetic resonance imaging |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498759/ https://www.ncbi.nlm.nih.gov/pubmed/26161747 http://dx.doi.org/10.1371/journal.pone.0132331 |
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