Diffusion tensor imaging detects age-dependent white matter changes in a transgenic mouse model with amyloid deposition

被引:153
作者
Song, SK
Kim, JH
Lin, SJ
Brendza, RP
Holtzman, DM
机构
[1] Washington Univ, Sch Med, Biomed MR Lab, Dept Radiol, St Louis, MO 63110 USA
[2] Washington Univ, Dept Chem, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Ctr Study Nervous Syst Injury, St Louis, MO 63110 USA
关键词
Alzheimer's disease; diffusion tenser; mice; PDAPP; MRI; myelin; axon; white matter;
D O I
10.1016/j.nbd.2003.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Increasing evidence demonstrates that there is marked damage and dysfunction not only in the gray matter but also in the white matter in Alzheimer's disease (AD). In this study, transgenic mice overexpressing beta-amyloid precursor protein (APP) under control of the platelet-derived growth factor promoter (PDAPP mice) were examined using diffusion tensor magnetic resonance imaging (DTI) to evaluate the extent of white matter injury before and following the development of AD-like pathology. The profile of DTI parameters was significantly different in old PDAPP mice compared to that of old control mice following the development of AD-like pathology. No difference in DTI parameters was observed between the young PDAPP and control mice. Our results suggest that as amyloid 0 (A) deposition and levels increase over time in PDAPP mice, these changes lead to primary or secondary white matter injury that can be detected by DTI. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:640 / 647
页数:8
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