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Mild cognitive impairment as a diagnostic entity.轻度认知障碍作为一种诊断实体。
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Medial temporal lobe function and structure in mild cognitive impairment.轻度认知障碍患者的内侧颞叶功能与结构
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Cortical synaptic integration in vivo is disrupted by amyloid-beta plaques.体内的皮质突触整合受到β-淀粉样蛋白斑的破坏。
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Use of IQ-adjusted norms to predict progressive cognitive decline in highly intelligent older individuals.使用智商调整后的常模来预测高智商老年人的渐进性认知衰退。
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Cognitive reserve-mediated modulation of positron emission tomographic activations during memory tasks in Alzheimer disease.认知储备对阿尔茨海默病记忆任务期间正电子发射断层扫描激活的调节作用
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Temporal cortex hypermetabolism in Down syndrome prior to the onset of dementia.唐氏综合征患者在痴呆症发作前颞叶皮质代谢亢进。
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fMRI differences in encoding and retrieval of pictures due to encoding strategy in the elderly.老年人中因编码策略导致的图片编码与检索过程中的功能磁共振成像差异。
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Alterations in the BOLD fMRI signal with ageing and disease: a challenge for neuroimaging.衰老和疾病导致的血氧水平依赖性功能磁共振成像(BOLD fMRI)信号改变:神经影像学面临的一项挑战
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Looking backward to move forward: early detection of neurodegenerative disorders.回首往昔,展望未来:神经退行性疾病的早期检测
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Putting names to faces: successful encoding of associative memories activates the anterior hippocampal formation.将名字与面孔对应:关联记忆的成功编码激活前海马结构。
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与正常衰老和阿尔茨海默病相比,轻度认知障碍患者海马体激活增加。

Increased hippocampal activation in mild cognitive impairment compared to normal aging and AD.

作者信息

Dickerson B C, Salat D H, Greve D N, Chua E F, Rand-Giovannetti E, Rentz D M, Bertram L, Mullin K, Tanzi R E, Blacker D, Albert M S, Sperling R A

机构信息

Department of Neurology, The Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Neurology. 2005 Aug 9;65(3):404-11. doi: 10.1212/01.wnl.0000171450.97464.49.

DOI:10.1212/01.wnl.0000171450.97464.49
PMID:16087905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4335677/
Abstract

OBJECTIVE

To use fMRI to investigate whether hippocampal and entorhinal activation during learning is altered in the earliest phase of mild cognitive impairment (MCI).

METHODS

Three groups of older individuals were studied: 10 cognitively intact controls, 9 individuals at the mild end of the spectrum of MCI, and 10 patients with probable Alzheimer disease (AD). Subjects performed a face-name associative encoding task during fMRI scanning, and were tested for recognition of stimuli afterward. Data were analyzed using a functional-anatomic method in which medial temporal lobe (MTL) regions of interest were identified from each individual's structural MRI, and fMRI activation was quantified within each region.

RESULTS

Significantly greater hippocampal activation was present in the MCI group compared to controls; there were no differences between these two groups in hippocampal or entorhinal volumes. In contrast, the AD group showed hippocampal and entorhinal hypoactivation and atrophy in comparison to controls. The subjects with MCI performed similarly to controls on the fMRI recognition memory task; patients with AD exhibited poorer performance. Across all 29 subjects, greater mean entorhinal activation was found in the subgroup of 13 carriers of the APOE epsilon4 allele than in the 16 noncarriers.

CONCLUSIONS

The authors hypothesize that there is a phase of increased medial temporal lobe activation early in the course of prodromal Alzheimer disease followed by a subsequent decrease as the disease progresses.

摘要

目的

使用功能磁共振成像(fMRI)研究在轻度认知障碍(MCI)的最早阶段,学习过程中海马体和内嗅皮层的激活是否发生改变。

方法

对三组老年人进行了研究:10名认知功能正常的对照组、9名处于MCI谱系轻度阶段的个体以及10名可能患有阿尔茨海默病(AD)的患者。受试者在fMRI扫描期间执行面孔-名字联想编码任务,之后进行刺激识别测试。使用功能解剖学方法分析数据,其中从每个个体的结构磁共振成像(MRI)中识别出内侧颞叶(MTL)感兴趣区域,并在每个区域内对fMRI激活进行量化。

结果

与对照组相比,MCI组的海马体激活明显更强;这两组在海马体或内嗅皮层体积上没有差异。相比之下,AD组与对照组相比表现出海马体和内嗅皮层激活不足以及萎缩。MCI受试者在fMRI识别记忆任务中的表现与对照组相似;AD患者表现较差。在所有29名受试者中,与16名非携带者相比,13名APOE ε4等位基因携带者亚组的平均内嗅皮层激活更强。

结论

作者推测,在阿尔茨海默病前驱期病程早期存在内侧颞叶激活增加的阶段,随后随着疾病进展而下降。