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Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease

BACKGROUND: To investigate the association between cerebral amyloid deposition and long‐term cognitive outcomes in patients with hemorrhagic small vessel disease (SVD) and survivors of intracerebral hemorrhage (ICH). METHODS: Patients experiencing an ICH without overt dementia were prospectively rec...

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Autores principales: Tsai, Ya‐Chin, Tsai, Hsin‐Hsi, Liu, Chia‐Ju, Lin, Sheng‐Sian, Chen, Ya‐Fang, Jeng, Jiann‐Shing, Tsai, Li‐Kai, Yen, Ruoh‐Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570474/
https://www.ncbi.nlm.nih.gov/pubmed/37533346
http://dx.doi.org/10.1002/brb3.3189
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author Tsai, Ya‐Chin
Tsai, Hsin‐Hsi
Liu, Chia‐Ju
Lin, Sheng‐Sian
Chen, Ya‐Fang
Jeng, Jiann‐Shing
Tsai, Li‐Kai
Yen, Ruoh‐Fang
author_facet Tsai, Ya‐Chin
Tsai, Hsin‐Hsi
Liu, Chia‐Ju
Lin, Sheng‐Sian
Chen, Ya‐Fang
Jeng, Jiann‐Shing
Tsai, Li‐Kai
Yen, Ruoh‐Fang
author_sort Tsai, Ya‐Chin
collection PubMed
description BACKGROUND: To investigate the association between cerebral amyloid deposition and long‐term cognitive outcomes in patients with hemorrhagic small vessel disease (SVD) and survivors of intracerebral hemorrhage (ICH). METHODS: Patients experiencing an ICH without overt dementia were prospectively recruited (n = 68) for brain MRI and Pittsburgh compound B (PiB) positron emission tomography scans at baseline. Cognitive function was assessed using the mini‐mental status examination (MMSE) and clinical dementia rating after an overall median follow‐up of 3.8 years. A positive amyloid scan was defined as a global PiB standardized uptake value ratio >1.2. Associations between follow‐up cognitive outcomes and neuroimaging markers were explored using multivariable Cox regression models. RESULTS: PiB(+) patients were older (72.1 ± 7.8 vs. 59.9 ± 11.7, p = .002) and more frequently had cerebral amyloid angiopathy (CAA) (63.6% vs. 15.8%, p = .002) than PiB(−) patients. PiB(+) was associated with a higher risk of dementia conversion (32.9 vs. 4.0 per 100‐person‐years, hazard ratio [HR] = 15.7 [3.0–80.7], p = .001) and MMSE score decline (58.8 vs. 9.9 per 100‐person‐years, HR = 6.2 [1.9–20.0], p = .002). In the non‐CAA subgroup (n = 52), PiB(+) remained an independent predictor of dementia conversion, p = .04). In the Cox models, PiB(+) was an independent predictor of dementia conversion (HR = 15.8 [2.6–95.4], p = .003) and MMSE score decline (HR = 5.7 [1.6–20.3], p = .008) after adjusting for confounders. CONCLUSIONS: Cerebral amyloid deposition potentially contributes to long‐term cognitive decline in SVD‐related ICH.
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spelling pubmed-105704742023-10-14 Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease Tsai, Ya‐Chin Tsai, Hsin‐Hsi Liu, Chia‐Ju Lin, Sheng‐Sian Chen, Ya‐Fang Jeng, Jiann‐Shing Tsai, Li‐Kai Yen, Ruoh‐Fang Brain Behav Original Articles BACKGROUND: To investigate the association between cerebral amyloid deposition and long‐term cognitive outcomes in patients with hemorrhagic small vessel disease (SVD) and survivors of intracerebral hemorrhage (ICH). METHODS: Patients experiencing an ICH without overt dementia were prospectively recruited (n = 68) for brain MRI and Pittsburgh compound B (PiB) positron emission tomography scans at baseline. Cognitive function was assessed using the mini‐mental status examination (MMSE) and clinical dementia rating after an overall median follow‐up of 3.8 years. A positive amyloid scan was defined as a global PiB standardized uptake value ratio >1.2. Associations between follow‐up cognitive outcomes and neuroimaging markers were explored using multivariable Cox regression models. RESULTS: PiB(+) patients were older (72.1 ± 7.8 vs. 59.9 ± 11.7, p = .002) and more frequently had cerebral amyloid angiopathy (CAA) (63.6% vs. 15.8%, p = .002) than PiB(−) patients. PiB(+) was associated with a higher risk of dementia conversion (32.9 vs. 4.0 per 100‐person‐years, hazard ratio [HR] = 15.7 [3.0–80.7], p = .001) and MMSE score decline (58.8 vs. 9.9 per 100‐person‐years, HR = 6.2 [1.9–20.0], p = .002). In the non‐CAA subgroup (n = 52), PiB(+) remained an independent predictor of dementia conversion, p = .04). In the Cox models, PiB(+) was an independent predictor of dementia conversion (HR = 15.8 [2.6–95.4], p = .003) and MMSE score decline (HR = 5.7 [1.6–20.3], p = .008) after adjusting for confounders. CONCLUSIONS: Cerebral amyloid deposition potentially contributes to long‐term cognitive decline in SVD‐related ICH. John Wiley and Sons Inc. 2023-08-02 /pmc/articles/PMC10570474/ /pubmed/37533346 http://dx.doi.org/10.1002/brb3.3189 Text en © 2023 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tsai, Ya‐Chin
Tsai, Hsin‐Hsi
Liu, Chia‐Ju
Lin, Sheng‐Sian
Chen, Ya‐Fang
Jeng, Jiann‐Shing
Tsai, Li‐Kai
Yen, Ruoh‐Fang
Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
title Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
title_full Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
title_fullStr Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
title_full_unstemmed Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
title_short Cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
title_sort cerebral amyloid deposition predicts long‐term cognitive decline in hemorrhagic small vessel disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570474/
https://www.ncbi.nlm.nih.gov/pubmed/37533346
http://dx.doi.org/10.1002/brb3.3189
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