The effects of aging and Alzheimer's disease on cerebral cortical anatomy: Specificity and differential relationships with cognition

被引:192
作者
Bakkour, Akram [1 ,2 ,4 ]
Morris, John C. [7 ,8 ]
Wolk, David A. [9 ]
Dickerson, Bradford C. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Massachusetts Gen Hosp, Frontotemporal Dementia Unit, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Massachusetts Alzheimers Dis Res Ctr, Boston, MA 02114 USA
[6] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Boston, MA 02114 USA
[7] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[8] Washington Univ, Sch Med, Alzheimers Dis Res Ctr, St Louis, MO USA
[9] Univ Penn, Dept Neurol, Alzheimers Dis Core Ctr, Penn Memory Ctr, Philadelphia, PA 19104 USA
关键词
Magnetic resonance imaging; Cerebral cortex; Aging; Alzheimer' disease; Parietal lobe; Frontal lobe; Temporal lobe; NORMAL NEUROANATOMICAL VARIATION; VOXEL-BASED MORPHOMETRY; SURFACE-BASED ANALYSIS; MEDIAL TEMPORAL-LOBE; BRAIN ATROPHY; AMYLOID DEPOSITION; AD DEMENTIA; MRI; AGE; CORTEX;
D O I
10.1016/j.neuroimage.2013.02.059
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Although both normal aging and Alzheimer's disease (AD) are associated with regional cortical atrophy, few studies have directly compared the spatial patterns and magnitude of effects of these two processes. The extant literature has not addressed two important questions: 1) Is the pattern of age-related cortical atrophy different if cognitively intact elderly individuals with silent AD pathology are excluded?.and 2) Does the age- or AD-related atrophy relate to cognitive function? Here we studied 142 young controls, 87 older controls, and 28 mild AD patients. In addition, we studied 35 older controls with neuroimaging data indicating the absence of brain amyloid. Whole-cortex analyses identified regions of interest (ROIs) of cortical atrophy in aging and in AD. Results showed that some regions are predominantly affected by age with relatively little additional atrophy in patients with AD, e.g., calcarine cortex; other regions are predominantly affected by AD with much less of an effect of age, e.g., medial temporal cortex. Finally, other regions are affected by both aging and AD, e.g., dorsolateral prefrontal cortex and inferior parietal lobule. Thus, the processes of aging and AD have both differential and partially overlapping effects on specific regions of the cerebral cortex. In particular, some frontoparietal regions are affected by both processes, most temporal lobe regions are affected much more prominently by AD than aging, while sensorimotor and some prefrontal regions are affected specifically by aging and minimally more by AD. Within normal older adults, atrophy in aging-specific cortical regions relates to cognitive performance, while in AD patients atrophy in AD-specific regions relates to cognitive performance. Further work is warranted to investigate the behavioral and clinical relevance of these findings in additional detail, as well as their histological basis; ROIs generated from the present study could be used strategically in such investigations. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:332 / 344
页数:13
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