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White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging
INTRODUCTION: The aim of this study was to examine white matter hyperintensities (WMH) and fractional anisotropy (FA) in empirically derived incident mild cognitive impairment (MCI) subtypes. METHODS: We evaluated 188 participants with incident MCI in the Mayo Clinic Study of Aging (MCSA) identified...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719426/ https://www.ncbi.nlm.nih.gov/pubmed/35005199 http://dx.doi.org/10.1002/dad2.12269 |
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author | Machulda, Mary M. Lundt, Emily S. Mester, Carly T. Albertson, Sabrina M. Raghavan, Sheelakumari Reid, Robert I. Schwarz, Christopher G. Graff‐Radford, Jonathan Jack, Clifford R. Knopman, David S. Mielke, Michelle M. Kremers, Walter K. Petersen, Ronald C. Bondi, Mark W. Vemuri, Prashanthi |
author_facet | Machulda, Mary M. Lundt, Emily S. Mester, Carly T. Albertson, Sabrina M. Raghavan, Sheelakumari Reid, Robert I. Schwarz, Christopher G. Graff‐Radford, Jonathan Jack, Clifford R. Knopman, David S. Mielke, Michelle M. Kremers, Walter K. Petersen, Ronald C. Bondi, Mark W. Vemuri, Prashanthi |
author_sort | Machulda, Mary M. |
collection | PubMed |
description | INTRODUCTION: The aim of this study was to examine white matter hyperintensities (WMH) and fractional anisotropy (FA) in empirically derived incident mild cognitive impairment (MCI) subtypes. METHODS: We evaluated 188 participants with incident MCI in the Mayo Clinic Study of Aging (MCSA) identified as having one of four cluster‐derived subtypes: subtle cognitive impairment, amnestic, dysnomic, and dysexecutive. We used linear regression models to evaluate whole brain and regional WMH volumes. We examined fractional anisotropy (FA) on a subset of 63 participants with diffusion tensor imaging. RESULTS: Amnestic and dysexecutive subtypes had higher WMH volumes in differing patterns than cognitively unimpaired; the dysexecutive subtype had higher WMH than subtle cognitive impairment. There was widespread WM degeneration in long association and commissural fibers in the amnestic, dysnomic, and dysexecutive subtypes, and corpus callosum FA accounted for significant variability in global cognition. DISCUSSION: White matter changes likely contribute to cognitive symptoms in incident MCI. |
format | Online Article Text |
id | pubmed-8719426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87194262022-01-07 White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging Machulda, Mary M. Lundt, Emily S. Mester, Carly T. Albertson, Sabrina M. Raghavan, Sheelakumari Reid, Robert I. Schwarz, Christopher G. Graff‐Radford, Jonathan Jack, Clifford R. Knopman, David S. Mielke, Michelle M. Kremers, Walter K. Petersen, Ronald C. Bondi, Mark W. Vemuri, Prashanthi Alzheimers Dement (Amst) Neuroimaging INTRODUCTION: The aim of this study was to examine white matter hyperintensities (WMH) and fractional anisotropy (FA) in empirically derived incident mild cognitive impairment (MCI) subtypes. METHODS: We evaluated 188 participants with incident MCI in the Mayo Clinic Study of Aging (MCSA) identified as having one of four cluster‐derived subtypes: subtle cognitive impairment, amnestic, dysnomic, and dysexecutive. We used linear regression models to evaluate whole brain and regional WMH volumes. We examined fractional anisotropy (FA) on a subset of 63 participants with diffusion tensor imaging. RESULTS: Amnestic and dysexecutive subtypes had higher WMH volumes in differing patterns than cognitively unimpaired; the dysexecutive subtype had higher WMH than subtle cognitive impairment. There was widespread WM degeneration in long association and commissural fibers in the amnestic, dysnomic, and dysexecutive subtypes, and corpus callosum FA accounted for significant variability in global cognition. DISCUSSION: White matter changes likely contribute to cognitive symptoms in incident MCI. John Wiley and Sons Inc. 2021-12-31 /pmc/articles/PMC8719426/ /pubmed/35005199 http://dx.doi.org/10.1002/dad2.12269 Text en © 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Neuroimaging Machulda, Mary M. Lundt, Emily S. Mester, Carly T. Albertson, Sabrina M. Raghavan, Sheelakumari Reid, Robert I. Schwarz, Christopher G. Graff‐Radford, Jonathan Jack, Clifford R. Knopman, David S. Mielke, Michelle M. Kremers, Walter K. Petersen, Ronald C. Bondi, Mark W. Vemuri, Prashanthi White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging |
title | White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging |
title_full | White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging |
title_fullStr | White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging |
title_full_unstemmed | White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging |
title_short | White matter changes in empirically derived incident MCI subtypes in the Mayo Clinic Study of Aging |
title_sort | white matter changes in empirically derived incident mci subtypes in the mayo clinic study of aging |
topic | Neuroimaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719426/ https://www.ncbi.nlm.nih.gov/pubmed/35005199 http://dx.doi.org/10.1002/dad2.12269 |
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