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Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease

BACKGROUND: Blood–brain barrier (BBB) damage is considered an important part of Alzheimer's disease (AD) progression, and cerebral small-vessel disease (CSVD) is commonly associated with AD. However, the relationship between BBB damage, small cerebrovascular lesions, especially cerebral microbl...

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Autores principales: Cheng, Zhaozhao, Dai, Linbin, Wu, Yan, Cao, Yuqin, Chai, Xianliang, Wang, Peng, Liu, Chang, Ni, Ming, Gao, Feng, Wang, Qiong, Lv, Xinyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978776/
https://www.ncbi.nlm.nih.gov/pubmed/36873442
http://dx.doi.org/10.3389/fneur.2023.1077860
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author Cheng, Zhaozhao
Dai, Linbin
Wu, Yan
Cao, Yuqin
Chai, Xianliang
Wang, Peng
Liu, Chang
Ni, Ming
Gao, Feng
Wang, Qiong
Lv, Xinyi
author_facet Cheng, Zhaozhao
Dai, Linbin
Wu, Yan
Cao, Yuqin
Chai, Xianliang
Wang, Peng
Liu, Chang
Ni, Ming
Gao, Feng
Wang, Qiong
Lv, Xinyi
author_sort Cheng, Zhaozhao
collection PubMed
description BACKGROUND: Blood–brain barrier (BBB) damage is considered an important part of Alzheimer's disease (AD) progression, and cerebral small-vessel disease (CSVD) is commonly associated with AD. However, the relationship between BBB damage, small cerebrovascular lesions, especially cerebral microbleeds (CMBs), and amyloid and tau biomarkers remains controversial. Therefore, our study aimed to further investigate their association in our cohort of patients with AD. METHODS: A total of 139 individuals were divided into probable AD ((18)F-florbetapir PET positive, n = 101) and control group (cognitively normal, n = 38). The levels of cerebrospinal fluid (CSF) and plasma t-tau, p-tau181, Aβ40, Aβ42, and albumin were measured using corresponding commercial assay kits, and the CSF/plasma albumin ratio (Qalb), an indicator of BBB dysfunction, was calculated. CSVD burden and the number of CMBs were defined using magnetic resonance imaging. RESULTS: Patients with AD had higher Qalb (p = 0.0024), higher numbers of CMBs (p = 0.03), and greater CSVD burden (p < 0.0001). In the AD group, CMBs and CSVD correlated with a higher Qalb (p = 0.03), and the numbers of CMBs negatively correlated with CSF Aβ42 (p = 0.02). CONCLUSION: Blood–brain barrier damage was accompanied by a more severe burden of CSVD, including CMB, in patients with AD.
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spelling pubmed-99787762023-03-03 Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease Cheng, Zhaozhao Dai, Linbin Wu, Yan Cao, Yuqin Chai, Xianliang Wang, Peng Liu, Chang Ni, Ming Gao, Feng Wang, Qiong Lv, Xinyi Front Neurol Neurology BACKGROUND: Blood–brain barrier (BBB) damage is considered an important part of Alzheimer's disease (AD) progression, and cerebral small-vessel disease (CSVD) is commonly associated with AD. However, the relationship between BBB damage, small cerebrovascular lesions, especially cerebral microbleeds (CMBs), and amyloid and tau biomarkers remains controversial. Therefore, our study aimed to further investigate their association in our cohort of patients with AD. METHODS: A total of 139 individuals were divided into probable AD ((18)F-florbetapir PET positive, n = 101) and control group (cognitively normal, n = 38). The levels of cerebrospinal fluid (CSF) and plasma t-tau, p-tau181, Aβ40, Aβ42, and albumin were measured using corresponding commercial assay kits, and the CSF/plasma albumin ratio (Qalb), an indicator of BBB dysfunction, was calculated. CSVD burden and the number of CMBs were defined using magnetic resonance imaging. RESULTS: Patients with AD had higher Qalb (p = 0.0024), higher numbers of CMBs (p = 0.03), and greater CSVD burden (p < 0.0001). In the AD group, CMBs and CSVD correlated with a higher Qalb (p = 0.03), and the numbers of CMBs negatively correlated with CSF Aβ42 (p = 0.02). CONCLUSION: Blood–brain barrier damage was accompanied by a more severe burden of CSVD, including CMB, in patients with AD. Frontiers Media S.A. 2023-02-16 /pmc/articles/PMC9978776/ /pubmed/36873442 http://dx.doi.org/10.3389/fneur.2023.1077860 Text en Copyright © 2023 Cheng, Dai, Wu, Cao, Chai, Wang, Liu, Ni, Gao, Wang and Lv. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Cheng, Zhaozhao
Dai, Linbin
Wu, Yan
Cao, Yuqin
Chai, Xianliang
Wang, Peng
Liu, Chang
Ni, Ming
Gao, Feng
Wang, Qiong
Lv, Xinyi
Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease
title Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease
title_full Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease
title_fullStr Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease
title_full_unstemmed Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease
title_short Correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in Alzheimer's disease
title_sort correlation of blood–brain barrier leakage with cerebral small vessel disease including cerebral microbleeds in alzheimer's disease
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978776/
https://www.ncbi.nlm.nih.gov/pubmed/36873442
http://dx.doi.org/10.3389/fneur.2023.1077860
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