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阿尔茨海默病的低代谢亚型与合并的海马硬化和路易体病理改变有关。

Hypometabolic subtypes of AD are linked to comorbid hippocampal sclerosis and Lewy body pathology.

作者信息

Levin Fedor, Dyrba Martin, Teipel Stefan J, Grothe Michel J

机构信息

Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Rostock, Germany.

Department of Psychosomatic Medicine, Rostock University Medical Center, Rostock, Germany.

出版信息

Alzheimers Res Ther. 2025 Jul 25;17(1):172. doi: 10.1186/s13195-025-01796-6.

Abstract

BACKGROUND

Neuroimaging studies have identified distinct 'typical/neocortical' and 'limbic-predominant' hypometabolic subtypes of AD with different clinical and biomarker characteristics. We investigated associations of these subtypes with postmortem neuropathological measures in an observational study.

METHODS

Antemortem FDG-PET scans of 74 participants from the ADNI autopsy cohort were classified into previously described typical/neocortical and limbic-predominant subtype patterns. We used Bayesian regression and ANCOVA to test associations between the subtypes and neuropathological features.

RESULTS

Results were inconclusive for Thal phases, Braak stages, CERAD neuritic plaque scores, hippocampal tangle density, and TDP-43 pathology (BF between 0.447 and 1.146). However, the limbic-predominant subtype was associated with hippocampal sclerosis (BF = 3.842, moderate level of evidence), whereas the typical/neocortical subtype was associated with Lewy body pathology (BF = 10.093, strong level of evidence).

CONCLUSIONS

These findings highlight the influence of AD and non-AD-specific pathologies on neurodegeneration patterns and may provide directions for research into hypometabolic pattern analysis as an indirect marker of comorbid pathology.

摘要

背景

神经影像学研究已识别出具有不同临床和生物标志物特征的阿尔茨海默病(AD)的不同“典型/新皮质”和“边缘系统为主”低代谢亚型。我们在一项观察性研究中调查了这些亚型与死后神经病理学测量指标之间的关联。

方法

对来自ADNI尸检队列的74名参与者的生前氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)进行分类,分为先前描述的典型/新皮质和边缘系统为主的亚型模式。我们使用贝叶斯回归和协方差分析来检验亚型与神经病理学特征之间的关联。

结果

对于Thal分期、Braak分期、CERAD神经炎性斑块评分、海马体缠结密度和TDP-43病理学,结果尚无定论(贝叶斯因子在0.447至1.146之间)。然而,边缘系统为主的亚型与海马体硬化相关(贝叶斯因子=3.842,证据水平中等),而典型/新皮质亚型与路易体病理学相关(贝叶斯因子=10.093,证据水平强)。

结论

这些发现突出了AD和非AD特异性病理学对神经退行性变模式的影响,并可能为将低代谢模式分析作为合并病理学间接标志物的研究提供方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/174d/12291356/ac66487f0e2a/13195_2025_1796_Fig1_HTML.jpg

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