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Acta Neuropathol. 2022 Jul;144(1):27-44. doi: 10.1007/s00401-022-02444-1. Epub 2022 Jun 13.
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Paucity of Entorhinal Cortex Pathology of the Alzheimer's Type in SuperAgers with Superior Memory Performance.记忆力超群的超级老人中阿尔茨海默病类型的内嗅皮层病理不足。
Cereb Cortex. 2021 Jun 10;31(7):3177-3183. doi: 10.1093/cercor/bhaa409.
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What have we learned from cognition in the oldest-old.我们从最年长的人群的认知中学到了什么。
Curr Opin Neurol. 2021 Apr 1;34(2):258-265. doi: 10.1097/WCO.0000000000000910.
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The clinical promise of biomarkers of synapse damage or loss in Alzheimer's disease.阿尔茨海默病中突触损伤或丢失的生物标志物的临床前景。
Alzheimers Res Ther. 2020 Mar 2;12(1):21. doi: 10.1186/s13195-020-00588-4.
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Activated Microglia in Cortical White Matter Across Cognitive Aging Trajectories.认知衰老轨迹中皮质白质的活化小胶质细胞
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Cognitive trajectories and spectrum of neuropathology in SuperAgers: The first 10 cases.超级老人的认知轨迹和神经病理学谱:前 10 例。
Hippocampus. 2019 May;29(5):458-467. doi: 10.1002/hipo.22828. Epub 2018 Feb 5.
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Cortex. 2018 Feb;99:69-77. doi: 10.1016/j.cortex.2017.10.015. Epub 2017 Nov 8.
9
Rates of Cortical Atrophy in Adults 80 Years and Older With Superior vs Average Episodic Memory.80岁及以上具有卓越与平均情景记忆的成年人的皮质萎缩率。
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10
Variations in Acetylcholinesterase Activity within Human Cortical Pyramidal Neurons Across Age and Cognitive Trajectories.人类大脑皮质锥体神经元内乙酰胆碱酯酶活性随年龄和认知轨迹的变化。
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内侧前额叶皮层神经元大小的完整性是非凡认知老化的生物学基础。

Integrity of Neuronal Size in the Entorhinal Cortex Is a Biological Substrate of Exceptional Cognitive Aging.

机构信息

Mesulam Center for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.

Department of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.

出版信息

J Neurosci. 2022 Nov 9;42(45):8587-8594. doi: 10.1523/JNEUROSCI.0679-22.2022. Epub 2022 Sep 30.

DOI:10.1523/JNEUROSCI.0679-22.2022
PMID:36180225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9665923/
Abstract

Average aging is associated with a gradual decline of memory capacity. SuperAgers are humans ≥80 years of age who show exceptional episodic memory at least as good as individuals 20-30 years their junior. This study investigated whether neuronal integrity in the entorhinal cortex (ERC), an area critical for memory and selectively vulnerable to neurofibrillary degeneration, differentiated SuperAgers from cognitively healthy younger individuals, cognitively average peers ("Normal Elderly"), and individuals with amnestic mild cognitive impairment. Postmortem sections of the ERC were stained with cresyl violet to visualize neurons and immunostained with mouse monoclonal antibody PHF-1 to visualize neurofibrillary tangles. The cross-sectional area (i.e., size) of layer II and layer III/V ERC neurons were quantified. Two-thirds of total participants were female. Unbiased stereology was used to quantitate tangles in a subgroup of SuperAgers and Normal Elderly. Linear mixed-effect models were used to determine differences across groups. Quantitative measurements found that the soma size of layer II ERC neurons in postmortem brain specimens were significantly larger in SuperAgers compared with all groups ( < 0.05)-including younger individuals 20-30 years their junior ( < 0.005). SuperAgers had significantly fewer stereologically quantified Alzheimer's disease-related neurofibrillary tangles in layer II ERC than Normal Elderly ( < 0.05). This difference in tangle burden in layer II between SuperAgers and Normal Elderly suggests that tangle-bearing neurons may be prone to shrinkage during aging. The finding that SuperAgers show ERC layer II neurons that are substantially larger even compared with individuals 20-30 years younger is remarkable, suggesting that layer II ERC integrity is a biological substrate of exceptional memory in old age. Average aging is associated with a gradual decline of memory. Previous research shows that an area critical for memory, the entorhinal cortex (ERC), is susceptible to the early formation of Alzheimer's disease neuropathology, even during average (or typical) trajectories of aging. The Northwestern University SuperAging Research Program studies unique individuals known as SuperAgers, individuals ≥80 years old who show exceptional memory that is at least as good as individuals 20-30 years their junior. In this study, we show that SuperAgers harbor larger, healthier neurons in the ERC compared with their cognitively average same-aged peers, those with amnestic mild cognitive impairment, and - remarkably - even compared with individuals 20-30 years younger. We conclude that larger ERC neurons are a biological signature of the SuperAging trajectory.

摘要

平均衰老与记忆能力的逐渐下降有关。超级老人是指年龄在 80 岁以上、表现出至少与年轻 20-30 岁的个体相当出色的情景记忆的人类。本研究旨在调查内侧颞叶(ERC)中的神经元完整性是否可以区分超级老人与认知健康的年轻个体、认知正常的同龄个体(“正常老年人”)和有轻度认知障碍的个体。ERC 的组织切片用甲苯胺蓝染色以显示神经元,并用鼠单克隆抗体 PHF-1 免疫染色以显示神经纤维缠结。量化了 ERC 中 II 层和 III/V 层神经元的横截面积(即大小)。三分之二的参与者为女性。使用无偏立体学来定量超级老人和正常老年人亚组中的缠结。使用线性混合效应模型确定组间差异。定量测量发现,与所有组(<0.05)——包括年轻 20-30 岁的个体(<0.005)相比,超级老人死后大脑标本中 II 层 ERC 神经元的胞体大小明显更大。与正常老年人相比,超级老人 II 层中阿尔茨海默病相关的神经纤维缠结的立体学定量显著减少(<0.05)。超级老人和正常老年人之间 II 层缠结负担的这种差异表明,缠结神经元在衰老过程中可能容易收缩。值得注意的是,即使与年轻 20-30 岁的个体相比,超级老人的 ERC 层 II 神经元也明显更大,这表明 ERC 层 II 的完整性是老年时异常记忆的生物学基础。平均衰老与记忆的逐渐下降有关。先前的研究表明,内侧颞叶(ERC)是记忆的关键区域,容易受到阿尔茨海默病神经病理学的早期形成的影响,即使在平均(或典型)衰老轨迹中也是如此。西北大学超级老龄化研究计划研究了被称为超级老人的独特个体,这些个体年龄在 80 岁以上,表现出的记忆能力至少与年轻 20-30 岁的个体相当。在这项研究中,我们发现与认知正常的同龄个体、有轻度认知障碍的个体相比,超级老人的 ERC 中拥有更大、更健康的神经元,而且——值得注意的是——与年轻 20-30 岁的个体相比也是如此。我们得出的结论是,更大的 ERC 神经元是超级老龄化轨迹的生物学特征。