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[健康衰老中的脑成像:与阿尔茨海默病的对比]

[Cerebral imaging in healthy aging: contrast with Alzheimer disease].

作者信息

Desgranges B, Kalpouzos G, Eustache F

机构信息

Inserm-EPHE-Université de Caen Basse-Normandie, Unité 923, Laboratoire de Neuropsychologie, GIP Cyceron, CHU Côte de Nacre, 14033 Caen cedex, France.

出版信息

Rev Neurol (Paris). 2008 May;164 Suppl 3:S102-7. doi: 10.1016/S0035-3787(08)73299-5.

Abstract

With age, the brain undergoes both structural and functional alterations. Overall, the literature consistently reports global brain atrophy in normal adults, generally more pronounced in frontal areas. As a result of different methodologies and inclusion criteria, other brain areas have been the matter of conflicting findings, notably the hippocampus. Regarding resting-state PET studies, they have consistently highlighted a metabolic deterioration of the frontal and anterior cingulated cortices. By contrast, relatively few investigations have sought to identify those areas that remain intact with aging, or undergo the least deterioration. We report a study designed to establish a comprehensive profile of both structural and functional changes in the aging brain, using up-to-date voxel-based methodology in 45 optimally healthy subjects aged 20-83 years. One of the main findings is that the lesser structural deterioration of the anterior hippocampal region, together with the lesser functional alteration of the posterior cingulate cortex, appear to mark the parting of the ways between normal aging and Alzheimer's disease, which is characterized by early and prominent deterioration of both structures. This paper also deals with studies set out to establish the relationship between changes in episodic memory retrieval in normal aging on the one hand and gray matter volume and 18FDG uptake on the other hand. Frontal areas dysfunction is involved in memory decline in older subjects, at least in some conditions, a finding which clearly contrasts with that found in Alzheimer's disease where the hippocampus plays a key role. Finally, compensatory mechanisms are reviewed through activation studies which often show supplementary activations in old subjects compared to young as well as in Alzheimer's disease patients compared to healthy elderly subjects. Paradoxically, those mechanisms seem to be underpinned, at least partially, by frontal areas in both populations, but researches are needed to better identify which subregions are involved.

摘要

随着年龄增长,大脑会发生结构和功能上的改变。总体而言,文献一致报道正常成年人存在全脑萎缩,通常在额叶区域更为明显。由于采用了不同的方法和纳入标准,其他脑区一直存在相互矛盾的研究结果,尤其是海马体。关于静息态PET研究,这些研究一直强调额叶和前扣带回皮质的代谢恶化。相比之下,相对较少的研究试图确定那些随着年龄增长保持完整或恶化程度最小的脑区。我们报告了一项研究,该研究旨在利用最新的基于体素的方法,对45名年龄在20至83岁之间的健康状况最佳的受试者的衰老大脑的结构和功能变化建立全面的概况。主要发现之一是,前海马区较小的结构恶化,以及后扣带回皮质较小的功能改变,似乎标志着正常衰老与阿尔茨海默病之间的分道扬镳,阿尔茨海默病的特征是这两种结构早期且明显的恶化。本文还探讨了旨在建立正常衰老过程中情景记忆检索变化与灰质体积和18FDG摄取之间关系的研究。额叶功能障碍与老年受试者的记忆衰退有关,至少在某些情况下如此,这一发现与阿尔茨海默病中海马体起关键作用的情况形成鲜明对比。最后,通过激活研究对补偿机制进行了综述,这些研究通常显示,与年轻人相比,老年受试者以及与健康老年受试者相比,阿尔茨海默病患者存在额外的激活。矛盾的是,这些机制似乎至少部分地由这两个人群的额叶区域所支撑,但需要进一步研究以更好地确定哪些亚区域参与其中。

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