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纹状体中 18F-AV45 的摄取为阿尔茨海默病提供了超越皮质的额外见解。

Uptake of 18F-AV45 in the Putamen Provides Additional Insights into Alzheimer's Disease beyond the Cortex.

机构信息

Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV 89106, USA.

Department of Brain Health, University of Nevada Las Vegas (UNLV), Las Vegas, NV 89154, USA.

出版信息

Biomolecules. 2024 Jan 29;14(2):157. doi: 10.3390/biom14020157.

DOI:10.3390/biom14020157
PMID:38397394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10886857/
Abstract

Cortical uptake in brain amyloid positron emission tomography (PET) is increasingly used for the biological diagnosis of Alzheimer's disease (AD); however, the clinical and biological relevance of the striatum beyond the cortex in amyloid PET scans remains unclear. A total of 513 amyloid-positive participants having 18F-AV45 amyloid PET scans available were included in the analysis. The associations between cognitive scores and striatal uptake were analyzed. The participants were categorized into three groups based on the residual from the linear fitting between 18F-AV45 uptake in the putamen and the cortex in the order of HighP > MidP > LowP group. We then examined the differences between these three groups in terms of clinical diagnosis, genotype, CSF phosphorylated tau (ptau) concentration, hippocampal volume, entorhinal thickness, and cognitive decline rate to evaluate the additional insights provided by the putamen beyond the cortex. The 18F-AV45 uptake in the putamen was more strongly associated with ADAS-cog13 and MoCA scores ( < 0.001) compared to the uptake in the caudate nucleus. Despite comparable cortical uptakes, the HighP group had a two-fold higher risk of being ε4-homozygous or diagnosed with AD dementia compared to the LowP group. These three groups had significantly different CSF ptau concentration, hippocampal volume, entorhinal thickness, and cognitive decline rate. These findings suggest that the assessment of 18F-AV45 uptake in the putamen is of unique value for evaluating disease severity and predicting disease progression.

摘要

脑淀粉样蛋白正电子发射断层扫描(PET)中的皮质摄取越来越多地用于阿尔茨海默病(AD)的生物学诊断;然而,淀粉样 PET 扫描中皮质以外纹状体的临床和生物学相关性尚不清楚。共有 513 名 18F-AV45 淀粉样蛋白 PET 扫描阳性的参与者被纳入分析。分析了认知评分与纹状体摄取之间的相关性。根据纹状体和皮质之间 18F-AV45 摄取的线性拟合的残差,将参与者分为三组,即 HighP > MidP > LowP 组。然后,我们比较了这三组之间在临床诊断、基因型、脑脊液磷酸化 tau(ptau)浓度、海马体积、内嗅皮质厚度和认知下降率方面的差异,以评估纹状体除皮质以外提供的额外见解。纹状体的 18F-AV45 摄取与 ADAS-cog13 和 MoCA 评分的相关性更强(<0.001),与尾状核的摄取相比。尽管皮质摄取相当,HighP 组发生 ε4 纯合子或被诊断为 AD 痴呆的风险是 LowP 组的两倍。这三组的脑脊液 ptau 浓度、海马体积、内嗅皮质厚度和认知下降率有显著差异。这些发现表明,评估纹状体 18F-AV45 摄取对评估疾病严重程度和预测疾病进展具有独特的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/f97824c5bc63/biomolecules-14-00157-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/8aaede274d2b/biomolecules-14-00157-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/9e2055e0ac0c/biomolecules-14-00157-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/8e9f228af4ee/biomolecules-14-00157-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/1a2cd19d304f/biomolecules-14-00157-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/f97824c5bc63/biomolecules-14-00157-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/8aaede274d2b/biomolecules-14-00157-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/9e2055e0ac0c/biomolecules-14-00157-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/8e9f228af4ee/biomolecules-14-00157-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/1a2cd19d304f/biomolecules-14-00157-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaa/10886857/f97824c5bc63/biomolecules-14-00157-g005.jpg

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JAMA Neurol. 2022 Mar 1;79(3):228-243. doi: 10.1001/jamaneurol.2021.5216.
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Predicting clinical decline and conversion to Alzheimer's disease or dementia using novel Elecsys Aβ(1-42), pTau and tTau CSF immunoassays.使用新型 Elecsys Aβ(1-42)、pTau 和 tTau 脑脊液免疫分析物预测临床衰退和向阿尔茨海默病或痴呆的转化。
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Staging β-Amyloid Pathology With Amyloid Positron Emission Tomography.
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