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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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