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Improved Localizadon of Cortical Activity by Combining EEG and MEG with MRI Cortical Surface Reconstruction: A Linear Approach.通过将 EEG 和 MEG 与 MRI 皮质表面重建相结合来提高皮质活动的本地化:一种线性方法。
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The prevalence of cortical gray matter atrophy may be overestimated in the healthy aging brain.在健康的衰老大脑中,皮质灰质萎缩的患病率可能被高估了。
Neuropsychology. 2009 Sep;23(5):541-50. doi: 10.1037/a0016161.
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Regional rates of neocortical atrophy from normal aging to early Alzheimer disease.从正常衰老到早期阿尔茨海默病的新皮质萎缩区域发生率。
Neurology. 2009 Aug 11;73(6):457-65. doi: 10.1212/WNL.0b013e3181b16431.
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Minute effects of sex on the aging brain: a multisample magnetic resonance imaging study of healthy aging and Alzheimer's disease.性别对衰老大脑的微小影响:一项关于健康衰老和阿尔茨海默病的多样本磁共振成像研究
J Neurosci. 2009 Jul 8;29(27):8774-83. doi: 10.1523/JNEUROSCI.0115-09.2009.
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Age-associated alterations in cortical gray and white matter signal intensity and gray to white matter contrast.与年龄相关的皮质灰质和白质信号强度以及灰质与白质对比度的改变。
Neuroimage. 2009 Oct 15;48(1):21-8. doi: 10.1016/j.neuroimage.2009.06.074. Epub 2009 Jul 4.
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Consistent neuroanatomical age-related volume differences across multiple samples.跨多个样本的一致的神经解剖学与年龄相关的体积差异。
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Increased sensitivity to effects of normal aging and Alzheimer's disease on cortical thickness by adjustment for local variability in gray/white contrast: a multi-sample MRI study.通过调整灰质/白质对比度的局部变异性来提高对正常衰老和阿尔茨海默病对皮质厚度影响的敏感性:一项多样本MRI研究
Neuroimage. 2009 Oct 1;47(4):1545-57. doi: 10.1016/j.neuroimage.2009.05.084. Epub 2009 Jun 6.
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Longitudinal pattern of regional brain volume change differentiates normal aging from MCI.脑区体积变化的纵向模式可区分正常衰老与轻度认知障碍。
Neurology. 2009 Jun 2;72(22):1906-13. doi: 10.1212/WNL.0b013e3181a82634.
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Longitudinal progression of Alzheimer's-like patterns of atrophy in normal older adults: the SPARE-AD index.正常老年人中阿尔茨海默病样萎缩模式的纵向进展:SPARE-AD指数
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10
Structural MRI biomarkers for preclinical and mild Alzheimer's disease.用于临床前和轻度阿尔茨海默病的结构磁共振成像生物标志物
Hum Brain Mapp. 2009 Oct;30(10):3238-53. doi: 10.1002/hbm.20744.

健康衰老过程中明显出现的一年期脑萎缩。

One-year brain atrophy evident in healthy aging.

作者信息

Fjell Anders M, Walhovd Kristine B, Fennema-Notestine Christine, McEvoy Linda K, Hagler Donald J, Holland Dominic, Brewer James B, Dale Anders M

机构信息

Center for the Study of Human Cognition, Department of Psychology, University of Oslo, 0317 Oslo, Norway.

出版信息

J Neurosci. 2009 Dec 2;29(48):15223-31. doi: 10.1523/JNEUROSCI.3252-09.2009.

DOI:10.1523/JNEUROSCI.3252-09.2009
PMID:19955375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2827793/
Abstract

An accurate description of changes in the brain in healthy aging is needed to understand the basis of age-related changes in cognitive function. Cross-sectional magnetic resonance imaging (MRI) studies suggest thinning of the cerebral cortex, volumetric reductions of most subcortical structures, and ventricular expansion. However, there is a paucity of detailed longitudinal studies to support the cross-sectional findings. In the present study, 142 healthy elderly participants (60-91 years of age) were followed with repeated MRI, and were compared with 122 patients with mild to moderate Alzheimer's disease (AD). Volume changes were measured across the entire cortex and in 48 regions of interest. Cortical reductions in the healthy elderly were extensive after only 1 year, especially evident in temporal and prefrontal cortices, where annual decline was approximately 0.5%. All subcortical and ventricular regions except caudate nucleus and the fourth ventricle changed significantly over 1 year. Some of the atrophy occurred in areas vulnerable to AD, while other changes were observed in areas less characteristic of the disease in early stages. This suggests that the changes are not primarily driven by degenerative processes associated with AD, although it is likely that preclinical changes associated with AD are superposed on changes due to normal aging in some subjects, especially in the temporal lobes. Finally, atrophy was found to accelerate with increasing age, and this was especially prominent in areas vulnerable to AD. Thus, it is possible that the accelerating atrophy with increasing age is due to preclinical AD.

摘要

为了理解认知功能中与年龄相关变化的基础,需要对健康衰老过程中大脑的变化进行准确描述。横断面磁共振成像(MRI)研究表明,大脑皮层变薄,大多数皮层下结构体积减小,脑室扩大。然而,缺乏详细的纵向研究来支持这些横断面研究结果。在本研究中,对142名健康老年参与者(60 - 91岁)进行了重复MRI跟踪,并与122名轻度至中度阿尔茨海默病(AD)患者进行了比较。测量了整个皮层和48个感兴趣区域的体积变化。健康老年人的皮层减少在仅1年后就很广泛,在颞叶和前额叶皮层尤为明显,每年下降约0.5%。除尾状核和第四脑室外,所有皮层下和脑室区域在1年内都有显著变化。一些萎缩发生在易患AD的区域,而其他变化则出现在疾病早期不太典型的区域。这表明这些变化并非主要由与AD相关的退行性过程驱动,尽管在一些受试者中,尤其是颞叶,与AD相关的临床前变化可能叠加在正常衰老引起的变化之上。最后,发现萎缩随着年龄增长而加速,这在易患AD的区域尤为突出。因此,年龄增长导致的萎缩加速可能是由于临床前AD。