| NEUROBIOLOGY OF AGING | 卷:31 |
| Sex and age differences in atrophic rates: an ADNI study with n=1368 MRI scans | |
| Article | |
| Hua, Xue1  Hibar, Derrek P.1  Lee, Suh1  Toga, Arthur W.1  Jack, Clifford R., Jr.2  Weiner, Michael W.3,4,5,6  Thompson, Paul M.1  | |
| [1] Univ Calif Los Angeles, Sch Med, Dept Neurol, Lab Neuro Imaging, Los Angeles, CA 90095 USA | |
| [2] Mayo Clin, Dept Radiol, Rochester, MN USA | |
| [3] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA | |
| [4] Univ Calif San Francisco, Dept Med, San Francisco, CA USA | |
| [5] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA 94143 USA | |
| [6] Vet Affairs Med Ctr, San Francisco, CA 94121 USA | |
| 关键词: Alzheimer's disease; Mild cognitive impairment; MRI; Longitudinal; Tensor-based morphometry; Age; Sex effect; Atrophy rate; Neuroimaging; Biomarker; Drug trial enrichment; | |
| DOI : 10.1016/j.neurobiolaging.2010.04.033 | |
| 来源: Elsevier | |
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【 摘 要 】
We set out to determine factors that influence the rate of brain atrophy in 1-year longitudinal magnetic resonance imaging (MRI) data. With tensor-based morphometry (TBM), we mapped the 3-dimensional profile of progressive atrophy in 144 subjects with probable Alzheimer's disease (AD) (age: 76.5 +/- 7.4 years), 338 with amnestic mild cognitive impairment (MCI; 76.0 +/- 7.2), and 202 healthy controls (77.0 +/- 5.1), scanned twice, 1 year apart. Statistical maps revealed significant age and sex differences in atrophic rates. Brain atrophic rates were about 1%-1.5% faster in women than men. Atrophy was faster in younger than older subjects, most prominently in mild cognitive impairment, with a 1% increase in the rates of atrophy and 2% in ventricular expansion, for every 10-year decrease in age. TBM-derived atrophic rates correlated with reduced beta-amyloid and elevated tau levels (n = 363) at baseline, baseline and progressive deterioration in clinical measures, and increasing numbers of risk alleles for the ApoE4 gene. TBM is a sensitive, high-throughput biomarker for tracking disease progression in large imaging studies; sub-analyses focusing on women or younger subjects gave improved sample size requirements for clinical trials. (C) 2010 Elsevier Inc. All rights reserved.
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| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_neurobiolaging_2010_04_033.pdf | 1868KB |
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