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骨质疏松症与老年人脑脊液生物标志物基线升高及脑结构萎缩加速有关。

Osteoporosis is associated with elevated baseline cerebrospinal fluid biomarkers and accelerated brain structural atrophy among older people.

作者信息

Pan Hao, Cao Jiali, Wu Congcong, Huang Furong, Wu Peng, Lang Junzhe, Liu Yangbo

机构信息

Department of Orthopedics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Department of Outpatient, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Front Aging Neurosci. 2022 Sep 16;14:958050. doi: 10.3389/fnagi.2022.958050. eCollection 2022.

Abstract

OBJECTIVE

The aim of this study was to examine whether osteoporosis (OP) is associated with Alzheimer's disease-related cerebrospinal fluid (CSF) biomarkers and brain structures among older people.

METHODS

From the Alzheimer's disease Neuroimaging Initiative database, we grouped participants according to the OP status (OP+/OP-) and compared the Alzheimer's disease (AD)-related CSF biomarker levels and the regional brain structural volumes between the two groups using multivariable models. These models were adjusted for covariates including age, education, gender, diagnosis of Alzheimer's disease, and apolipoprotein E4 carrier status.

RESULTS

In the cross-sectional analyses at baseline, OP was related to higher CSF t-tau (total tau) and p-tau (tau phosphorylated at threonine-181) but not to CSF amyloid-beta (1-42) or the volumes of entorhinal cortex and hippocampus. In the longitudinal analyses, OP was not associated with the change in the three CSF biomarkers over time but was linked to a faster decline in the size of the entorhinal cortex and hippocampus.

CONCLUSION

OP was associated with elevated levels of CSF t-tau and p-tau at baseline, and accelerated entorhinal cortex and hippocampal atrophies over time among older people.

摘要

目的

本研究旨在探讨老年人骨质疏松症(OP)是否与阿尔茨海默病相关的脑脊液(CSF)生物标志物及脑结构有关。

方法

从阿尔茨海默病神经影像学倡议数据库中,我们根据OP状态(OP+/OP-)对参与者进行分组,并使用多变量模型比较两组之间与阿尔茨海默病(AD)相关的CSF生物标志物水平和脑区结构体积。这些模型针对年龄、教育程度、性别、阿尔茨海默病诊断及载脂蛋白E4携带者状态等协变量进行了调整。

结果

在基线时的横断面分析中,OP与较高的CSF总tau蛋白(t-tau)和苏氨酸-181位点磷酸化tau蛋白(p-tau)相关,但与CSFβ淀粉样蛋白(1-42)或内嗅皮质及海马体积无关。在纵向分析中,OP与三种CSF生物标志物随时间的变化无关,但与内嗅皮质和海马体积的更快缩小有关。

结论

在老年人中,OP与基线时CSF中t-tau和p-tau水平升高相关,且随着时间推移与内嗅皮质和海马萎缩加速有关。

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