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Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment

BACKGROUND AND PURPOSE: Poststroke cognitive impairment (PSCI) is common, but the impact of β-amyloid (Aβ) on PSCI is uncertain. The proposed study will investigate amyloid pathology in participants with PSCI and how differently their cognition progress according to the amyloid pathology. METHODS: T...

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Autores principales: Yoon, Bora, Yang, Dong Won, Hong, Yun-Jeong, Kim, Taewon, Na, Seunghee, Noh, Sang-Mi, Park, Hye Lim, Ku, Bon D., Yang, Young Soon, Choi, Hojin, Jang, Jae-Won, Kim, Seongheon, Kim, Yerim, Shim, YongSoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462636/
https://www.ncbi.nlm.nih.gov/pubmed/34559128
http://dx.doi.org/10.1097/MD.0000000000027252
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author Yoon, Bora
Yang, Dong Won
Hong, Yun-Jeong
Kim, Taewon
Na, Seunghee
Noh, Sang-Mi
Park, Hye Lim
Ku, Bon D.
Yang, Young Soon
Choi, Hojin
Jang, Jae-Won
Kim, Seongheon
Kim, Yerim
Shim, YongSoo
author_facet Yoon, Bora
Yang, Dong Won
Hong, Yun-Jeong
Kim, Taewon
Na, Seunghee
Noh, Sang-Mi
Park, Hye Lim
Ku, Bon D.
Yang, Young Soon
Choi, Hojin
Jang, Jae-Won
Kim, Seongheon
Kim, Yerim
Shim, YongSoo
author_sort Yoon, Bora
collection PubMed
description BACKGROUND AND PURPOSE: Poststroke cognitive impairment (PSCI) is common, but the impact of β-amyloid (Aβ) on PSCI is uncertain. The proposed study will investigate amyloid pathology in participants with PSCI and how differently their cognition progress according to the amyloid pathology. METHODS: This multicenter study was designed to be prospective and observational based on a projected cohort size of 196 participants with either newly developed cognitive impairment, or rapidly aggravated CI, within 3 months after acute cerebral infarction. They will undergo (18)F-flutemetamol positron emission tomography at baseline and will be categorized as either amyloid-positive (A+) or amyloid-negative (A−) by visual rating. The primary outcome measures will be based on Korean Mini-Mental State Examination changes (baseline to 12 months) between the A+ and A− groups. The secondary outcome measures will be the dementia-conversion rate and changes in the Korean version of the Montreal Cognitive Assessment (baseline to 12 months) between the A+ and A− groups. CONCLUSIONS: This study will provide a broadened perspective on the impact of Aβ on the cause and outcomes of PSCI in clinical practice. Identifying amyloid pathology in patients with PSCI will help select patients who need more focused treatments such as acetylcholinesterase inhibitors TRIAL REGISTRATION: Clinical Research Information Service identifier: KCT0005086
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spelling pubmed-84626362021-09-27 Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment Yoon, Bora Yang, Dong Won Hong, Yun-Jeong Kim, Taewon Na, Seunghee Noh, Sang-Mi Park, Hye Lim Ku, Bon D. Yang, Young Soon Choi, Hojin Jang, Jae-Won Kim, Seongheon Kim, Yerim Shim, YongSoo Medicine (Baltimore) 5300 BACKGROUND AND PURPOSE: Poststroke cognitive impairment (PSCI) is common, but the impact of β-amyloid (Aβ) on PSCI is uncertain. The proposed study will investigate amyloid pathology in participants with PSCI and how differently their cognition progress according to the amyloid pathology. METHODS: This multicenter study was designed to be prospective and observational based on a projected cohort size of 196 participants with either newly developed cognitive impairment, or rapidly aggravated CI, within 3 months after acute cerebral infarction. They will undergo (18)F-flutemetamol positron emission tomography at baseline and will be categorized as either amyloid-positive (A+) or amyloid-negative (A−) by visual rating. The primary outcome measures will be based on Korean Mini-Mental State Examination changes (baseline to 12 months) between the A+ and A− groups. The secondary outcome measures will be the dementia-conversion rate and changes in the Korean version of the Montreal Cognitive Assessment (baseline to 12 months) between the A+ and A− groups. CONCLUSIONS: This study will provide a broadened perspective on the impact of Aβ on the cause and outcomes of PSCI in clinical practice. Identifying amyloid pathology in patients with PSCI will help select patients who need more focused treatments such as acetylcholinesterase inhibitors TRIAL REGISTRATION: Clinical Research Information Service identifier: KCT0005086 Lippincott Williams & Wilkins 2021-09-24 /pmc/articles/PMC8462636/ /pubmed/34559128 http://dx.doi.org/10.1097/MD.0000000000027252 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 5300
Yoon, Bora
Yang, Dong Won
Hong, Yun-Jeong
Kim, Taewon
Na, Seunghee
Noh, Sang-Mi
Park, Hye Lim
Ku, Bon D.
Yang, Young Soon
Choi, Hojin
Jang, Jae-Won
Kim, Seongheon
Kim, Yerim
Shim, YongSoo
Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
title Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
title_full Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
title_fullStr Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
title_full_unstemmed Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
title_short Cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
title_sort cognitive decline according to amyloid uptake in patients with poststroke cognitive impairment
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462636/
https://www.ncbi.nlm.nih.gov/pubmed/34559128
http://dx.doi.org/10.1097/MD.0000000000027252
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