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Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease
Background: The underlying white matter impairment in patients with early and late-onset Alzheimer’s disease (EOAD and LOAD) is still unclear, and this might due to the complex AD pathology. Methods: We included 31 EOAD, 45 LOAD, and 64 younger, 46 elder controls in our study to undergo MRI examinat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148465/ https://www.ncbi.nlm.nih.gov/pubmed/33930871 http://dx.doi.org/10.18632/aging.202702 |
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author | Luo, Xiao Wang, Shuyue Jiaerken, Yeerfan Li, Kaicheng Zeng, Qingze Zhang, Ruiting Wang, Chao Xu, Xiaopei Wu, Dan Huang, Peiyu Zhang, Minming |
author_facet | Luo, Xiao Wang, Shuyue Jiaerken, Yeerfan Li, Kaicheng Zeng, Qingze Zhang, Ruiting Wang, Chao Xu, Xiaopei Wu, Dan Huang, Peiyu Zhang, Minming |
author_sort | Luo, Xiao |
collection | PubMed |
description | Background: The underlying white matter impairment in patients with early and late-onset Alzheimer’s disease (EOAD and LOAD) is still unclear, and this might due to the complex AD pathology. Methods: We included 31 EOAD, 45 LOAD, and 64 younger, 46 elder controls in our study to undergo MRI examinations. Fiber density (FD) and fiber bundle cross-section (FC) were measured using fixel-based analysis based on diffusion weighted images. On whole brain and tract-based level, we compared these parameters among different groups (p<0.05, FWE corrected). Moreover, we verified our results in another independent dataset using the same analyses. Results: Compared to young healthy controls, EOAD had significantly lower FD in the splenium of corpus callosum, limbic tracts, cingulum bundles, and posterior thalamic radiation, and higher FC in the splenium of corpus callosum, dorsal cingulum and posterior thalamic radiation. On the other hand, LOAD had lower FD and FC as well. Importantly, a similar pattern was found in the independent validation dataset. Among all groups, both the FD and FC were associated with cognitive function. Furthermore, FD of fornix column and body, and FC of ventral cingulum were associated with composite amyloid and tau level (r=-0.34 and -0.53, p<0.001) respectively. Conclusions: EOAD and LOAD were characterized by distinct white matter impairment patterns, which may be attributable to their different neuropathologies. |
format | Online Article Text |
id | pubmed-8148465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-81484652021-05-26 Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease Luo, Xiao Wang, Shuyue Jiaerken, Yeerfan Li, Kaicheng Zeng, Qingze Zhang, Ruiting Wang, Chao Xu, Xiaopei Wu, Dan Huang, Peiyu Zhang, Minming Aging (Albany NY) Research Paper Background: The underlying white matter impairment in patients with early and late-onset Alzheimer’s disease (EOAD and LOAD) is still unclear, and this might due to the complex AD pathology. Methods: We included 31 EOAD, 45 LOAD, and 64 younger, 46 elder controls in our study to undergo MRI examinations. Fiber density (FD) and fiber bundle cross-section (FC) were measured using fixel-based analysis based on diffusion weighted images. On whole brain and tract-based level, we compared these parameters among different groups (p<0.05, FWE corrected). Moreover, we verified our results in another independent dataset using the same analyses. Results: Compared to young healthy controls, EOAD had significantly lower FD in the splenium of corpus callosum, limbic tracts, cingulum bundles, and posterior thalamic radiation, and higher FC in the splenium of corpus callosum, dorsal cingulum and posterior thalamic radiation. On the other hand, LOAD had lower FD and FC as well. Importantly, a similar pattern was found in the independent validation dataset. Among all groups, both the FD and FC were associated with cognitive function. Furthermore, FD of fornix column and body, and FC of ventral cingulum were associated with composite amyloid and tau level (r=-0.34 and -0.53, p<0.001) respectively. Conclusions: EOAD and LOAD were characterized by distinct white matter impairment patterns, which may be attributable to their different neuropathologies. Impact Journals 2021-04-30 /pmc/articles/PMC8148465/ /pubmed/33930871 http://dx.doi.org/10.18632/aging.202702 Text en Copyright: © 2021 Luo et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Luo, Xiao Wang, Shuyue Jiaerken, Yeerfan Li, Kaicheng Zeng, Qingze Zhang, Ruiting Wang, Chao Xu, Xiaopei Wu, Dan Huang, Peiyu Zhang, Minming Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease |
title | Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease |
title_full | Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease |
title_fullStr | Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease |
title_full_unstemmed | Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease |
title_short | Distinct fiber-specific white matter reductions pattern in early- and late-onset Alzheimer’s disease |
title_sort | distinct fiber-specific white matter reductions pattern in early- and late-onset alzheimer’s disease |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148465/ https://www.ncbi.nlm.nih.gov/pubmed/33930871 http://dx.doi.org/10.18632/aging.202702 |
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