Age-related white matter integrity differences in oldest-old without dementia

被引:27
作者
Bennett, Ilana J. [1 ]
Greenia, Dana E. [2 ]
Maillard, Pauline [3 ]
Sajjadi, S. Ahmad [4 ]
DeCarli, Charles [3 ,5 ]
Corrada, Maria M. [2 ,4 ,6 ]
Kawas, Claudia H. [2 ,4 ,6 ,7 ]
机构
[1] Univ Calif Riverside, Dept Psychol, 900 Univ Ave, Riverside, CA 92521 USA
[2] Univ Calif Irvine, Inst Memory Impairments & Neurol Disorders, Irvine, CA USA
[3] Univ Calif Davis, Dept Neurol, Davis, CA 95616 USA
[4] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
[5] Univ Calif Davis, Alzheimers Dis Ctr, Davis, CA 95616 USA
[6] Univ Calif Davis, Dept Epidemiol, Davis, CA 95616 USA
[7] Univ Calif Davis, Dept Neurobiol & Behav, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
Aging; White matter integrity; Oldest-old; Corpus callosum; Fornix; HUMAN BRAIN; ALZHEIMERS-DISEASE; NERVE-FIBERS; DIFFUSION; VULNERABILITY; DECLINE; MEMORY; MYELIN;
D O I
10.1016/j.neurobiolaging.2017.04.013
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Aging is known to have deleterious effects on cerebral white matter, yet little is known about these white matter alterations in advanced age. In this study, 94 oldest-old adults without dementia (90-103 years) underwent diffusion tensor imaging to assess relationships between chronological age and multiple measures of integrity in 18 white matter regions across the brain. Results revealed significant age-related declines in integrity in regions previously identified as being sensitive to aging in younger-old adults (corpus callosum, fornix, cingulum, external capsule). For the corpus callosum, the effect of age on genu fractional anisotropy was significantly weaker than the relationship between age and splenium fractional anisotropy. Importantly, age-related declines in white matter integrity did not differ in cognitively normal and cognitively impaired not demented oldest-old, suggesting that they were not solely driven by cognitive dysfunction or preclinical dementia in this advanced age group. Instead, white matter in these regions appears to remain vulnerable to normal aging processes through the 10th decade of life. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 114
页数:7
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