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Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study
BACKGROUND: Hippocampal atrophy is a key pathologic and magnetic resonance imaging (MRI) feature of human Alzheimer’s disease (AD). Hippocampal atrophy has not been documented via MRI in canine cognitive dysfunction (CCD), which is considered as the dog model of human AD. AIM: The purpose of this re...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculty of Veterinary Medicine
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830179/ https://www.ncbi.nlm.nih.gov/pubmed/33614439 http://dx.doi.org/10.4314/ovj.v10i4.11 |
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author | Dewey, Curtis Wells Rishniw, Mark Johnson, Philippa J. Platt, Simon Robinson, Kelsey Sackman, Joseph O’Donnell, Marissa |
author_facet | Dewey, Curtis Wells Rishniw, Mark Johnson, Philippa J. Platt, Simon Robinson, Kelsey Sackman, Joseph O’Donnell, Marissa |
author_sort | Dewey, Curtis Wells |
collection | PubMed |
description | BACKGROUND: Hippocampal atrophy is a key pathologic and magnetic resonance imaging (MRI) feature of human Alzheimer’s disease (AD). Hippocampal atrophy has not been documented via MRI in canine cognitive dysfunction (CCD), which is considered as the dog model of human AD. AIM: The purpose of this retrospective comparative volumetric MRI study was to compare total hippocampal volumes between successfully aging (control) dogs and dogs diagnosed with CCD. METHODS: Mimics(®) software was used to derive total hippocampal volumes and total brain volumes from the MRI studies of 42 aging dogs (≥ 9 years): 16 dogs diagnosed with CCD and 26 successfully aging controls. Hippocampal volumes were normalized to total brain volume and these values were compared between groups using Mann–Whitney U tests. RESULTS: Total hippocampal volume normalized to total brain volume was significantly less for CCD patients compared with control dogs (p = 0.04). CONCLUSION: The results of this study suggest that – similar to human AD – hippocampal atrophy is a pathological feature of CCD. This finding has potential importance for both investigating disease mechanisms related to dementia as well as future hippocampal-targeted therapies. |
format | Online Article Text |
id | pubmed-7830179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Faculty of Veterinary Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-78301792021-02-19 Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study Dewey, Curtis Wells Rishniw, Mark Johnson, Philippa J. Platt, Simon Robinson, Kelsey Sackman, Joseph O’Donnell, Marissa Open Vet J Original Research BACKGROUND: Hippocampal atrophy is a key pathologic and magnetic resonance imaging (MRI) feature of human Alzheimer’s disease (AD). Hippocampal atrophy has not been documented via MRI in canine cognitive dysfunction (CCD), which is considered as the dog model of human AD. AIM: The purpose of this retrospective comparative volumetric MRI study was to compare total hippocampal volumes between successfully aging (control) dogs and dogs diagnosed with CCD. METHODS: Mimics(®) software was used to derive total hippocampal volumes and total brain volumes from the MRI studies of 42 aging dogs (≥ 9 years): 16 dogs diagnosed with CCD and 26 successfully aging controls. Hippocampal volumes were normalized to total brain volume and these values were compared between groups using Mann–Whitney U tests. RESULTS: Total hippocampal volume normalized to total brain volume was significantly less for CCD patients compared with control dogs (p = 0.04). CONCLUSION: The results of this study suggest that – similar to human AD – hippocampal atrophy is a pathological feature of CCD. This finding has potential importance for both investigating disease mechanisms related to dementia as well as future hippocampal-targeted therapies. Faculty of Veterinary Medicine 2020 2020-12-01 /pmc/articles/PMC7830179/ /pubmed/33614439 http://dx.doi.org/10.4314/ovj.v10i4.11 Text en http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Dewey, Curtis Wells Rishniw, Mark Johnson, Philippa J. Platt, Simon Robinson, Kelsey Sackman, Joseph O’Donnell, Marissa Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study |
title |
Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study |
title_full |
Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study |
title_fullStr |
Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study |
title_full_unstemmed |
Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study |
title_short |
Canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: A comparative magnetic resonance imaging study |
title_sort | canine cognitive dysfunction patients have reduced total hippocampal volume compared with aging control dogs: a comparative magnetic resonance imaging study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830179/ https://www.ncbi.nlm.nih.gov/pubmed/33614439 http://dx.doi.org/10.4314/ovj.v10i4.11 |
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