Using voxel-based morphometry to map the structural changes associated with rapid conversion in MCI:: A longitudinal MRI study

被引:418
作者
Chételat, G
Landeau, B
Eustache, F
Mézenge, F
Viader, F
de la Sayette, V
Desgranges, B
Baron, JC
机构
[1] Univ Caen, INSERM E0218, Neuropsychol Lab, Ctr Cyceron, F-14074 Caen, France
[2] Univ Paris 05, EPHE, CNRS, UMR 8581, Paris 5, France
[3] CHU Caen, Serv Neurol Vastel, Caen, France
[4] Univ Cambridge, Dept Neurol, Cambridge CB2 1TN, England
关键词
Alzheimer's disease; mild cognitive impairment; longitudinal MRI; brain mapping; gray matter loss;
D O I
10.1016/j.neuroimage.2005.05.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Capturing the dynamics of gray matter (GM) atrophy in relation to the conversion from mild cognitive impairment (MCI) to clinically probable Alzheimer's disease (AD) would be of considerable interest. In this prospective study we have used a novel longitudinal voxel-based method to map the progression of GM loss in MCI patients over time and compared converters to non-converters. Eighteen amnestic MCI patients were followed-up for a predefined fixed period of 18 months and conversion was judged according to NINCDS-ADRDA criteria for probable AD. Each patient underwent a high-resolution T1-weighted volume MRI scan both at entry in the study and 18 months later. We used an optimal VBM protocol to compare baseline imaging data of converters to those of non-converters. Moreover, to map GM loss from baseline to follow-up assessment, we used a modified voxel-based morphometry (VBM) procedure specially designed for longitudinal studies. At the end of the follow-up period, seven patients had converted to probable AD. Areas of lower baseline GM value in converters mainly included the hippocampus, parahippocampal cortex, and lingual and fusiform gyri. Regions of significant GM loss over the 18-month follow-up period common to both converters and non-converters included the temporal neocortex, parahippocampal cortex, orbitofrontal and inferior parietal areas, and the left thalamus. However, there was significantly greater GM loss in converters relative to non-converters in the hippocampal area, inferior and middle temporal gyros, posterior cingulate, and precuneus. This accelerated atrophy may result from both neurofibrillary tangles accumulation and parallel pathological processes such as functional alteration in the posterior cingulate. The ability to longitudinally assess GM changes in MCI offers new perspectives to better understand the pathological processes underlying AD and to monitor the effects of treatment on brain structure. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:934 / 946
页数:13
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