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Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features
INTRODUCTION: Although widespread cortical asymmetries have been identified in Alzheimer's disease (AD), thalamic asymmetries and their relevance to clinical severity in AD remain unclear. METHODS: Lateralization indices were computed for individual thalamic subnuclei of 65 participants (33 hea...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811895/ https://www.ncbi.nlm.nih.gov/pubmed/31667328 http://dx.doi.org/10.1016/j.dadm.2019.08.001 |
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author | Low, Audrey Mak, Elijah Malpetti, Maura Chouliaras, Leonidas Nicastro, Nicolas Su, Li Holland, Negin Rittman, Timothy Rodríguez, Patricia Vázquez Passamonti, Luca Bevan-Jones, W Richard Jones, PP Simon Rowe, James B. O'Brien, John T. |
author_facet | Low, Audrey Mak, Elijah Malpetti, Maura Chouliaras, Leonidas Nicastro, Nicolas Su, Li Holland, Negin Rittman, Timothy Rodríguez, Patricia Vázquez Passamonti, Luca Bevan-Jones, W Richard Jones, PP Simon Rowe, James B. O'Brien, John T. |
author_sort | Low, Audrey |
collection | PubMed |
description | INTRODUCTION: Although widespread cortical asymmetries have been identified in Alzheimer's disease (AD), thalamic asymmetries and their relevance to clinical severity in AD remain unclear. METHODS: Lateralization indices were computed for individual thalamic subnuclei of 65 participants (33 healthy controls, 14 amyloid-positive patients with mild cognitive impairment, and 18 patients with AD dementia). We compared lateralization indices across diagnostic groups and correlated them with clinical measures. RESULTS: Although overall asymmetry of the thalamus did not differ between groups, greater leftward lateralization of atrophy in the ventral nuclei was demonstrated in AD, compared with controls and amyloid-positive mild cognitive impairment. Increased posterior ventrolateral and ventromedial nuclei asymmetry were associated with worse cognitive dysfunction, informant-reported neuropsychiatric symptoms, and functional ability. DISCUSSION: Leftward ventral thalamic atrophy was associated with disease severity in AD. Our findings suggest the clinically relevant involvement of thalamic nuclei in the pathophysiology of AD. |
format | Online Article Text |
id | pubmed-6811895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68118952019-10-30 Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features Low, Audrey Mak, Elijah Malpetti, Maura Chouliaras, Leonidas Nicastro, Nicolas Su, Li Holland, Negin Rittman, Timothy Rodríguez, Patricia Vázquez Passamonti, Luca Bevan-Jones, W Richard Jones, PP Simon Rowe, James B. O'Brien, John T. Alzheimers Dement (Amst) Neuroimaging INTRODUCTION: Although widespread cortical asymmetries have been identified in Alzheimer's disease (AD), thalamic asymmetries and their relevance to clinical severity in AD remain unclear. METHODS: Lateralization indices were computed for individual thalamic subnuclei of 65 participants (33 healthy controls, 14 amyloid-positive patients with mild cognitive impairment, and 18 patients with AD dementia). We compared lateralization indices across diagnostic groups and correlated them with clinical measures. RESULTS: Although overall asymmetry of the thalamus did not differ between groups, greater leftward lateralization of atrophy in the ventral nuclei was demonstrated in AD, compared with controls and amyloid-positive mild cognitive impairment. Increased posterior ventrolateral and ventromedial nuclei asymmetry were associated with worse cognitive dysfunction, informant-reported neuropsychiatric symptoms, and functional ability. DISCUSSION: Leftward ventral thalamic atrophy was associated with disease severity in AD. Our findings suggest the clinically relevant involvement of thalamic nuclei in the pathophysiology of AD. Elsevier 2019-10-01 /pmc/articles/PMC6811895/ /pubmed/31667328 http://dx.doi.org/10.1016/j.dadm.2019.08.001 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Neuroimaging Low, Audrey Mak, Elijah Malpetti, Maura Chouliaras, Leonidas Nicastro, Nicolas Su, Li Holland, Negin Rittman, Timothy Rodríguez, Patricia Vázquez Passamonti, Luca Bevan-Jones, W Richard Jones, PP Simon Rowe, James B. O'Brien, John T. Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
title | Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
title_full | Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
title_fullStr | Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
title_full_unstemmed | Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
title_short | Asymmetrical atrophy of thalamic subnuclei in Alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
title_sort | asymmetrical atrophy of thalamic subnuclei in alzheimer's disease and amyloid-positive mild cognitive impairment is associated with key clinical features |
topic | Neuroimaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811895/ https://www.ncbi.nlm.nih.gov/pubmed/31667328 http://dx.doi.org/10.1016/j.dadm.2019.08.001 |
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