Spatial patterns of cortical thinning in mild cognitive impairment and Alzheimer's disease

被引:288
|
作者
Singh, Vivek
Chertkow, Howard
Lerch, Jason P.
Evans, Alan C.
Dorr, Adrienne E.
Kabani, Noor Jehan
机构
[1] Sunnybrook & Womens Coll Hlth Sci Ctr, Toronto, ON, Canada
[2] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[3] Lady Davis Inst, Montreal, PQ, Canada
[4] Montreal Neurol Inst, McConnell Brain Imaging Ctr, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
Alzheimer's disease; brain imaging; cerebral cortex; dementia; mild cognitive impairment;
D O I
10.1093/brain/awl256
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cortical thickness is a more reliable measure of atrophy than volume due to the low variability in the cytoarchitectural structure of the grey matter. However, this more desirable measure of disease-related alterations is not fully evaluated in early dementia. The study presented here is the first to report the spatial patterns of cortical thickness in the pre-clinical stages of Alzheimer's disease, namely mild cognitive impairment (MCI). Cortical thickness measurements for 34 healthy elderly, 62 MCI and 42 Alzheimer's disease subjects were made using fully automated magnetic resonance imaging-based analysis techniques in order to determine the pattern of cortical thinning as a function of disease progression. The thickness of the cortex decreased significantly when the healthy elderly brains were compared to those with MCI, mainly in the medial temporal lobe region and in some regions of the frontal and the parietal cortices. With the progression of disease from MCI to Alzheimer's disease, a general thinning of the entire cortex with significant extension into the lateral temporal lobe was found. In all cases, the results were more pronounced in the left hemisphere. In conclusion, we have shown that there is a specific pattern in the thinning of the cortical ribbon which is in agreement with the previous histological reports. These novel findings support the notion of increased isocortical involvement with the progression of disease.
引用
收藏
页码:2885 / 2893
页数:9
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