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Cerebrospinal Fluid Neurofilament Light Predicts Risk of Dementia Onset in Cognitively Healthy Individuals and Rate of Cognitive Decline in Mild Cognitive Impairment: A Prospective Longitudinal Study.脑脊液神经丝轻链可预测认知健康个体的痴呆发病风险及轻度认知障碍个体的认知衰退速度:一项前瞻性纵向研究
Biomedicines. 2022 Apr 30;10(5):1045. doi: 10.3390/biomedicines10051045.
2
Relationship between cerebrospinal fluid neurodegeneration biomarkers and temporal brain atrophy in cognitively healthy older adults.认知健康老年人的脑脊液神经退行性生物标志物与颞叶脑萎缩的关系。
Neurobiol Aging. 2022 Aug;116:80-91. doi: 10.1016/j.neurobiolaging.2022.04.010. Epub 2022 Apr 22.
3
Interrelations of Alzheimer´s disease candidate biomarkers neurogranin, fatty acid-binding protein 3 and ferritin to neurodegeneration and neuroinflammation.阿尔茨海默病候选生物标志物神经颗粒蛋白、脂肪酸结合蛋白 3 和铁蛋白与神经退行性变和神经炎症的相互关系。
J Neurochem. 2021 Jun;157(6):2210-2224. doi: 10.1111/jnc.15175. Epub 2020 Sep 18.
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Involvement of Lipids in Alzheimer's Disease Pathology and Potential Therapies.脂质在阿尔茨海默病病理学中的作用及潜在治疗方法
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Biomarker profiling beyond amyloid and tau: cerebrospinal fluid markers, hippocampal atrophy, and memory change in cognitively unimpaired older adults.超越淀粉样蛋白和 tau 的生物标志物分析:认知正常的老年人的脑脊液标志物、海马萎缩和记忆变化。
Neurobiol Aging. 2020 Sep;93:1-15. doi: 10.1016/j.neurobiolaging.2020.04.002. Epub 2020 Apr 15.
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Neurology. 2019 Jul 23;93(4):e322-e333. doi: 10.1212/WNL.0000000000007831. Epub 2019 Jul 9.
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Effect of age, ethnicity, sex, cognitive status and APOE genotype on amyloid load and the threshold for amyloid positivity.年龄、种族、性别、认知状态和 APOE 基因型对淀粉样蛋白负荷和淀粉样蛋白阳性阈值的影响。
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9
A plasma protein classifier for predicting amyloid burden for preclinical Alzheimer's disease.用于预测临床前阿尔茨海默病淀粉样蛋白负担的血浆蛋白分类器。
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10
Cerebrospinal fluid biomarkers for understanding multiple aspects of Alzheimer's disease pathogenesis.用于了解阿尔茨海默病发病机制多个方面的脑脊液生物标志物。
Cell Mol Life Sci. 2019 May;76(10):1833-1863. doi: 10.1007/s00018-019-03040-5. Epub 2019 Feb 15.

认知健康个体中,脑脊液脂肪酸结合蛋白3水平与淀粉样病变的可能性相关。

Cerebrospinal fluid levels of fatty acid-binding protein 3 are associated with likelihood of amyloidopathy in cognitively healthy individuals.

作者信息

Dhiman Kunal, Villemagne Victor L, Fowler Christopher, Bourgeat Pierrick, Li Qiao-Xin, Collins Steven, Rowe Christopher C, Masters Colin L, Ames David, Blennow Kaj, Zetterberg Henrik, Martins Ralph N, Gupta Veer

机构信息

IMPACT - The Institute for Mental and Physical Health and Clinical Translation School of Medicine Deakin University Geelong Victoria Australia.

Western Health Partnership School of Nursing and Midwifery (Centre for Quality and Patient Safety Research in the Institute of Health Transformation) Faculty of Health Deakin University Melbourne Victoria Australia.

出版信息

Alzheimers Dement (Amst). 2022 Dec 4;14(1):e12377. doi: 10.1002/dad2.12377. eCollection 2022.

DOI:
10.1002/dad2.12377
PMID:36479019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9719998/
Abstract

INTRODUCTION

Fatty acid-binding protein 3 (FABP3) is a biomarker of neuronal membrane disruption, associated with lipid dyshomeostasis-a notable Alzheimer's disease (AD) pathophysiological change. We assessed the association of cerebrospinal fluid (CSF) FABP3 levels with brain amyloidosis and the likelihood/risk of developing amyloidopathy in cognitively healthy individuals.

METHODS

FABP3 levels were measured in CSF samples of cognitively healthy participants, > 60 years of age ( = 142), from the Australian Imaging, Biomarkers & Lifestyle Flagship Study of Ageing (AIBL).

RESULTS

FABP3 levels were positively associated with baseline brain amyloid beta (Aβ) load as measured by standardized uptake value ratio (SUVR, standardized  = 0.22, .009) and predicted the change in brain Aβ load (standardized  = 0.32, .004). Higher levels of CSF FABP3 (above median) were associated with a likelihood of amyloidopathy (odds ratio [OR] 2.28, 95% confidence interval [CI] 1.12 to 4.65, .023).

DISCUSSION

These results support inclusion of CSF FABP3 as a biomarker in risk-prediction models of AD.

摘要

引言

脂肪酸结合蛋白3(FABP3)是神经元膜破坏的生物标志物,与脂质稳态失衡相关,脂质稳态失衡是阿尔茨海默病(AD)显著的病理生理变化。我们评估了脑脊液(CSF)中FABP3水平与脑淀粉样变性的关联,以及认知健康个体发生淀粉样病变的可能性/风险。

方法

在澳大利亚衰老成像、生物标志物和生活方式旗舰研究(AIBL)中,对年龄大于60岁(n = 142)的认知健康参与者的脑脊液样本进行FABP3水平检测。

结果

FABP3水平与通过标准化摄取值比率(SUVR)测量的基线脑淀粉样β蛋白(Aβ)负荷呈正相关(标准化β = 0.22,P = 0.009),并预测脑Aβ负荷的变化(标准化β = 0.32,P = 0.004)。脑脊液FABP3水平较高(高于中位数)与淀粉样病变的可能性相关(比值比[OR] 2.28,95%置信区间[CI] 1.12至4.65,P = 0.023)。

讨论

这些结果支持将脑脊液FABP3纳入AD风险预测模型中的生物标志物。