Associations between cerebrospinal fluid biomarkers related to endothelial dysfunction and Alzheimer's disease.

IF 5.2 2区 医学 Q2 GERIATRICS & GERONTOLOGY
Frontiers in Aging Neuroscience Pub Date : 2026-09-21 eCollection Date: 2026-01-01 DOI:10.3389/fnagi.2026.1744647
Yang-Ke Zhu, Qiu-Jie Zhu, Lan-Yang Wang, He-Ying Hu, Xue-Jie Wang, Zi-Hao Zhang, Wei Zhang, Lan Tan, Hao Hu
{"title":"Associations between cerebrospinal fluid biomarkers related to endothelial dysfunction and Alzheimer's disease.","authors":"Yang-Ke Zhu, Qiu-Jie Zhu, Lan-Yang Wang, He-Ying Hu, Xue-Jie Wang, Zi-Hao Zhang, Wei Zhang, Lan Tan, Hao Hu","doi":"10.3389/fnagi.2026.1744647","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Although associations between overt vascular injury and Alzheimer's disease (AD) have been reported, the role of subclinical vascular injury in dementia pathogenesis remains unclear. Cerebrospinal fluid (CSF) biomarkers related to endothelial dysfunction may capture subclinical vascular impairment and provide insights into early AD pathogenesis.</p><p><strong>Methods: </strong>We examined associations of ten CSF biomarkers (PDGFRβ, Osteopontin, VCAM-1, E-selectin, MMP-2, MMP-10, MMP-3, MMP-12, MMP-9/TIMP-1 ratio and Periostin) with AD core biomarkers, brain volume, cognitive function, and risk of incident AD among 444 participants. Multivariable linear regression, linear mixed-effects models, Cox proportional hazards models, mediation analyses, and 3-year time-dependent ROC analyses were applied. All models were adjusted for demographic factors, <i>APOE</i> ε4 status, and vascular risk factors.</p><p><strong>Results: </strong>Seven of ten biomarkers were significantly associated with CSF tau biomarkers, whereas two biomarkers were associated with CSF Aβ<sub>42</sub>. Mediation analyses suggested that CSF tau biomarkers statistically accounted for a greater proportion of the associations between MMP-10 and cognition than did Aβ<sub>42</sub>. Among the biomarkers examined, MMP-10 showed the most consistent associations across AD-related outcomes, including lower CSF Aβ<sub>42</sub>, higher CSF tau biomarkers, poorer cognitive performance, greater longitudinal brain atrophy, and increased risk of incident AD dementia.</p><p><strong>Conclusion: </strong>Cerebrospinal fluid biomarkers related to endothelial dysfunction and vascular injury were more consistently associated with CSF tau biomarkers than with CSF Aβ<sub>42</sub> in non-demented individuals. MMP-10 showed the most consistent pathological, cognitive, neuroimaging, and prognostic associations and provided incremental predictive information for incident AD dementia. These findings support further investigation of endothelial dysfunction-related and vascular remodeling pathways as potential correlates of AD progression.</p>","PeriodicalId":12450,"journal":{"name":"Frontiers in Aging Neuroscience","volume":"18 ","pages":"1744647"},"PeriodicalIF":5.2000,"publicationDate":"2026-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13635297/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Aging Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnagi.2026.1744647","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Although associations between overt vascular injury and Alzheimer's disease (AD) have been reported, the role of subclinical vascular injury in dementia pathogenesis remains unclear. Cerebrospinal fluid (CSF) biomarkers related to endothelial dysfunction may capture subclinical vascular impairment and provide insights into early AD pathogenesis.

Methods: We examined associations of ten CSF biomarkers (PDGFRβ, Osteopontin, VCAM-1, E-selectin, MMP-2, MMP-10, MMP-3, MMP-12, MMP-9/TIMP-1 ratio and Periostin) with AD core biomarkers, brain volume, cognitive function, and risk of incident AD among 444 participants. Multivariable linear regression, linear mixed-effects models, Cox proportional hazards models, mediation analyses, and 3-year time-dependent ROC analyses were applied. All models were adjusted for demographic factors, APOE ε4 status, and vascular risk factors.

Results: Seven of ten biomarkers were significantly associated with CSF tau biomarkers, whereas two biomarkers were associated with CSF Aβ42. Mediation analyses suggested that CSF tau biomarkers statistically accounted for a greater proportion of the associations between MMP-10 and cognition than did Aβ42. Among the biomarkers examined, MMP-10 showed the most consistent associations across AD-related outcomes, including lower CSF Aβ42, higher CSF tau biomarkers, poorer cognitive performance, greater longitudinal brain atrophy, and increased risk of incident AD dementia.

Conclusion: Cerebrospinal fluid biomarkers related to endothelial dysfunction and vascular injury were more consistently associated with CSF tau biomarkers than with CSF Aβ42 in non-demented individuals. MMP-10 showed the most consistent pathological, cognitive, neuroimaging, and prognostic associations and provided incremental predictive information for incident AD dementia. These findings support further investigation of endothelial dysfunction-related and vascular remodeling pathways as potential correlates of AD progression.

与内皮功能障碍相关的脑脊液生物标志物与阿尔茨海默病之间的关系
背景:虽然有报道表明明显血管损伤与阿尔茨海默病(AD)之间存在关联,但亚临床血管损伤在痴呆发病机制中的作用尚不清楚。与内皮功能障碍相关的脑脊液(CSF)生物标志物可能捕获亚临床血管损伤,并为阿尔茨海默病的早期发病机制提供见解。方法:在444名参与者中,我们检测了10种脑脊液生物标志物(PDGFRβ、骨桥蛋白、VCAM-1、e -选择素、MMP-2、MMP-10、MMP-3、MMP-12、MMP-9/TIMP-1比率和Periostin)与AD核心生物标志物、脑容量、认知功能和AD发生风险的相关性。采用多变量线性回归、线性混合效应模型、Cox比例风险模型、中介分析和3年时间相关ROC分析。所有模型均根据人口统计学因素、APOE ε4状态和血管危险因素进行调整。结果:10个生物标志物中有7个与CSF tau生物标志物显著相关,而2个生物标志物与CSF a - β42相关。中介分析表明,脑脊液tau生物标志物在MMP-10和认知之间的关联中所占的比例比a β42要大。在检测的生物标志物中,MMP-10在AD相关结果中表现出最一致的相关性,包括脑脊液Aβ42降低,脑脊液tau生物标志物升高,认知能力下降,纵向脑萎缩加剧,AD痴呆风险增加。结论:在非痴呆个体中,与内皮功能障碍和血管损伤相关的脑脊液生物标志物与CSF tau生物标志物的相关性比与CSF Aβ42的相关性更一致。MMP-10表现出最一致的病理、认知、神经影像学和预后相关性,并为AD痴呆的发生提供了增量预测信息。这些发现支持进一步研究内皮功能障碍相关和血管重塑途径作为AD进展的潜在相关因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience GERIATRICS & GERONTOLOGY-NEUROSCIENCES
CiteScore
6.30
自引率
8.30%
发文量
1426
期刊介绍: Frontiers in Aging Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the mechanisms of Central Nervous System aging and age-related neural diseases. Specialty Chief Editor Thomas Wisniewski at the New York University School of Medicine is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书