Decreased white matter integrity in late-myelinating fiber pathways in Alzheimer's disease supports retrogenesis

被引:251
|
作者
Stricker, N. H. [2 ]
Schweinsburg, B. C. [3 ]
Delano-Wood, L. [1 ,4 ]
Wierenga, C. E. [1 ,4 ]
Bangen, K. J. [5 ]
Haaland, K. Y. [2 ,6 ,7 ,8 ]
Frank, L. R. [1 ]
Salmon, D. P. [9 ]
Bondi, M. W. [1 ,4 ]
机构
[1] VA San Diego Healthcare Syst, Psychol Serv 116B, San Diego, CA 92161 USA
[2] New Mexico VA Healthcare Syst, Albuquerque, NM USA
[3] Yale Univ, New Haven, CT 06520 USA
[4] Univ Calif San Diego, Sch Med, Dept Psychiat, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, San Diego State Univ, Joint Doctoral Program Clin Psychol, La Jolla, CA 92093 USA
[6] Univ New Mexico, Dept Psychiat, Albuquerque, NM 87131 USA
[7] Univ New Mexico, Dept Neurol, Albuquerque, NM 87131 USA
[8] Univ Calif San Diego, Dept Radiol, La Jolla, CA 92093 USA
[9] Univ Calif San Diego, Sch Med, Dept Neurosci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
MILD COGNITIVE IMPAIRMENT; DIFFUSION ANISOTROPY; TRACT INTEGRITY; MR-IMAGES; BRAIN; DEMENTIA; MODEL; MICROSTRUCTURE; DEGENERATION; MECHANISMS;
D O I
10.1016/j.neuroimage.2008.11.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The retrogenesis model of Alzheimer's disease (AD) posits that white matter (WM) degeneration follows a pattern that is the reverse of myelogenesis. Using diffusion tensor imaging (DTI) to test this model, we predicted greater loss of microstructural integrity in late-myelinating WM fiber pathways in AD patients than in healthy older adults, whereas differences in early-myelinating WM fiber pathways were not expected. We compared 16 AD patients and 14 demographically-matched healthy older adults with a whole-brain approach via tract-based spatial statistics (TBSS), and a region of interest (ROI) approach targeting early-myelinating (posterior limb of internal capsule, cerebral peduncles) and late-myelinating (inferior longitudinal fasciculus [ILF], superior longitudinal fasciculus [SLF]) fiber pathways. Permutation-based voxelwise analysis supported the retrogenesis model. There was significantly lower fractional anisotropy (FA) in AD patients compared to healthy older adults in late-myelinating but not early-myelinating pathways. These group differences appeared to be driven by loss of myelin integrity based on our finding of greater radial diffusion in AD than in healthy elderly. ROI analyses were generally in agreement with whole-brain findings, with significantly lower FA and increased radial diffusion in the ILF in the AD group. Consistent with the retrogenesis model, AD patients showed demonstrable changes in late-myelinating WM fiber pathways. Given greater change in the ILF than the SLF, wallerian degeneration secondary to cortical atrophy may also be a contributing mechanism. Knowledge of the pattern of WM microstructural changes in AD and its underlying mechanisms may contribute to earlier detection and intervention in at-risk groups. Published by Elsevier Inc.
引用
收藏
页码:10 / 16
页数:7
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