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Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease

INTRODUCTION: Present study was to investigate hs-CRP concentration, brain structural alterations, and cognitive function in the context of AD [Subjective cognitive decline (SCD), mild cognitive impairment (MCI), and AD]. METHODS: We retrospectively included 313 patients (Mean age = 76.40 years, 59...

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Autores principales: Zhang, Ye, Tatewaki, Yasuko, Nakase, Taizen, Liu, Yingxu, Tomita, Naoki, Thyreau, Benjamin, Zheng, Haixia, Muranaka, Michiho, Takano, Yumi, Nagasaka, Tatsuo, Taki, Yasuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427872/
https://www.ncbi.nlm.nih.gov/pubmed/37593375
http://dx.doi.org/10.3389/fnagi.2023.1227325
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author Zhang, Ye
Tatewaki, Yasuko
Nakase, Taizen
Liu, Yingxu
Tomita, Naoki
Thyreau, Benjamin
Zheng, Haixia
Muranaka, Michiho
Takano, Yumi
Nagasaka, Tatsuo
Taki, Yasuyuki
author_facet Zhang, Ye
Tatewaki, Yasuko
Nakase, Taizen
Liu, Yingxu
Tomita, Naoki
Thyreau, Benjamin
Zheng, Haixia
Muranaka, Michiho
Takano, Yumi
Nagasaka, Tatsuo
Taki, Yasuyuki
author_sort Zhang, Ye
collection PubMed
description INTRODUCTION: Present study was to investigate hs-CRP concentration, brain structural alterations, and cognitive function in the context of AD [Subjective cognitive decline (SCD), mild cognitive impairment (MCI), and AD]. METHODS: We retrospectively included 313 patients (Mean age = 76.40 years, 59 SCD, 101 MCI, 153 AD) in a cross-sectional analysis and 91 patients (Mean age = 75.83 years, 12 SCD, 43 MCI, 36 AD) in a longitudinal analysis. Multivariable linear regression was conducted to investigate the relationship between hs-CRP concentration and brain structural alterations, and cognitive function, respectively. RESULTS: Hs-CRP was positively associated with gray matter volume in the left fusiform (β = 0.16, p(FDR) = 0.023) and the left parahippocampal gyrus (β = 0.16, p(FDR) = 0.029). Post hoc analysis revealed that these associations were mainly driven by patients with MCI and AD. The interaction of diagnosis and CRP was significantly associated with annual cognitive changes (β = 0.43, p = 0.008). Among these patients with AD, lower baseline CRP was correlated with greater future cognitive decline (r = −0.41, p = 0.013). CONCLUSION: Our study suggests that increased hs-CRP level may exert protective effect on brain structure alterations and future cognitive changes among patients already with cognitive impairment.
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spelling pubmed-104278722023-08-17 Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease Zhang, Ye Tatewaki, Yasuko Nakase, Taizen Liu, Yingxu Tomita, Naoki Thyreau, Benjamin Zheng, Haixia Muranaka, Michiho Takano, Yumi Nagasaka, Tatsuo Taki, Yasuyuki Front Aging Neurosci Neuroscience INTRODUCTION: Present study was to investigate hs-CRP concentration, brain structural alterations, and cognitive function in the context of AD [Subjective cognitive decline (SCD), mild cognitive impairment (MCI), and AD]. METHODS: We retrospectively included 313 patients (Mean age = 76.40 years, 59 SCD, 101 MCI, 153 AD) in a cross-sectional analysis and 91 patients (Mean age = 75.83 years, 12 SCD, 43 MCI, 36 AD) in a longitudinal analysis. Multivariable linear regression was conducted to investigate the relationship between hs-CRP concentration and brain structural alterations, and cognitive function, respectively. RESULTS: Hs-CRP was positively associated with gray matter volume in the left fusiform (β = 0.16, p(FDR) = 0.023) and the left parahippocampal gyrus (β = 0.16, p(FDR) = 0.029). Post hoc analysis revealed that these associations were mainly driven by patients with MCI and AD. The interaction of diagnosis and CRP was significantly associated with annual cognitive changes (β = 0.43, p = 0.008). Among these patients with AD, lower baseline CRP was correlated with greater future cognitive decline (r = −0.41, p = 0.013). CONCLUSION: Our study suggests that increased hs-CRP level may exert protective effect on brain structure alterations and future cognitive changes among patients already with cognitive impairment. Frontiers Media S.A. 2023-08-01 /pmc/articles/PMC10427872/ /pubmed/37593375 http://dx.doi.org/10.3389/fnagi.2023.1227325 Text en Copyright © 2023 Zhang, Tatewaki, Nakase, Liu, Tomita, Thyreau, Zheng, Muranaka, Takano, Nagasaka and Taki. 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 Neuroscience
Zhang, Ye
Tatewaki, Yasuko
Nakase, Taizen
Liu, Yingxu
Tomita, Naoki
Thyreau, Benjamin
Zheng, Haixia
Muranaka, Michiho
Takano, Yumi
Nagasaka, Tatsuo
Taki, Yasuyuki
Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
title Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
title_full Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
title_fullStr Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
title_full_unstemmed Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
title_short Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
title_sort impact of hs-crp concentration on brain structure alterations and cognitive trajectory in alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427872/
https://www.ncbi.nlm.nih.gov/pubmed/37593375
http://dx.doi.org/10.3389/fnagi.2023.1227325
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