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Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy

We aimed to identify an Alzheimer’s disease (AD) subtype with right predominant focal atrophy. We recruited 17 amyloid PET positive logopenic variant primary progressive aphasia (lvPPA) and 226 amyloid PET positive AD patients. To identify AD with right focal atrophy (Rt-AD), we selected cortical ar...

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Autores principales: Kim, Ko Woon, Park, Seongbeom, Jo, Hyunjin, Cho, Soo Hyun, Kim, Seung Joo, Kim, Yeshin, Jang, Hyemin, Na, Duk L., Seo, Sang Won, Kim, Hee Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190862/
https://www.ncbi.nlm.nih.gov/pubmed/32350336
http://dx.doi.org/10.1038/s41598-020-64180-4
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author Kim, Ko Woon
Park, Seongbeom
Jo, Hyunjin
Cho, Soo Hyun
Kim, Seung Joo
Kim, Yeshin
Jang, Hyemin
Na, Duk L.
Seo, Sang Won
Kim, Hee Jin
author_facet Kim, Ko Woon
Park, Seongbeom
Jo, Hyunjin
Cho, Soo Hyun
Kim, Seung Joo
Kim, Yeshin
Jang, Hyemin
Na, Duk L.
Seo, Sang Won
Kim, Hee Jin
author_sort Kim, Ko Woon
collection PubMed
description We aimed to identify an Alzheimer’s disease (AD) subtype with right predominant focal atrophy. We recruited 17 amyloid PET positive logopenic variant primary progressive aphasia (lvPPA) and 226 amyloid PET positive AD patients. To identify AD with right focal atrophy (Rt-AD), we selected cortical areas that showed more atrophy in lvPPA than in AD and calculated an asymmetry index (AI) for this area in each individual. Using a receiver operating characteristic curve, we found that the optimal AI cut-off to discriminate lvPPA from AD was −3.1 (mean AI – 1.00 standard deviation) (sensitivity 88.2, specificity 89.8). We identified 32 Rt-AD patients whose AI was above mean AI + 1.00 standard deviation, 38 Lt-AD patients whose AI was lower than mean AI − 1.00 standard deviation, and 173 Symmetric-AD patients whose AI was within mean AI ± 1.00 standard deviation. We characterized clinical and cognitive profiles of Rt-AD patients by comparing with those of Lt-AD and Symmetric-AD patients. Compared to Symmetric-AD patients, Rt-AD patients had asymmetric focal atrophy in the right temporoparietal area and showed poor performance on visuospatial function testing (p = 0.009). Our findings suggested that there is an AD variant characterized by right focal atrophy and visuospatial dysfunction.
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spelling pubmed-71908622020-05-05 Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy Kim, Ko Woon Park, Seongbeom Jo, Hyunjin Cho, Soo Hyun Kim, Seung Joo Kim, Yeshin Jang, Hyemin Na, Duk L. Seo, Sang Won Kim, Hee Jin Sci Rep Article We aimed to identify an Alzheimer’s disease (AD) subtype with right predominant focal atrophy. We recruited 17 amyloid PET positive logopenic variant primary progressive aphasia (lvPPA) and 226 amyloid PET positive AD patients. To identify AD with right focal atrophy (Rt-AD), we selected cortical areas that showed more atrophy in lvPPA than in AD and calculated an asymmetry index (AI) for this area in each individual. Using a receiver operating characteristic curve, we found that the optimal AI cut-off to discriminate lvPPA from AD was −3.1 (mean AI – 1.00 standard deviation) (sensitivity 88.2, specificity 89.8). We identified 32 Rt-AD patients whose AI was above mean AI + 1.00 standard deviation, 38 Lt-AD patients whose AI was lower than mean AI − 1.00 standard deviation, and 173 Symmetric-AD patients whose AI was within mean AI ± 1.00 standard deviation. We characterized clinical and cognitive profiles of Rt-AD patients by comparing with those of Lt-AD and Symmetric-AD patients. Compared to Symmetric-AD patients, Rt-AD patients had asymmetric focal atrophy in the right temporoparietal area and showed poor performance on visuospatial function testing (p = 0.009). Our findings suggested that there is an AD variant characterized by right focal atrophy and visuospatial dysfunction. Nature Publishing Group UK 2020-04-29 /pmc/articles/PMC7190862/ /pubmed/32350336 http://dx.doi.org/10.1038/s41598-020-64180-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Ko Woon
Park, Seongbeom
Jo, Hyunjin
Cho, Soo Hyun
Kim, Seung Joo
Kim, Yeshin
Jang, Hyemin
Na, Duk L.
Seo, Sang Won
Kim, Hee Jin
Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy
title Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy
title_full Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy
title_fullStr Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy
title_full_unstemmed Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy
title_short Identifying a subtype of Alzheimer’s disease characterised by predominant right focal cortical atrophy
title_sort identifying a subtype of alzheimer’s disease characterised by predominant right focal cortical atrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190862/
https://www.ncbi.nlm.nih.gov/pubmed/32350336
http://dx.doi.org/10.1038/s41598-020-64180-4
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