Volume changes in Alzheimer's disease and mild cognitive impairment: cognitive associations

被引:77
作者
Evans, Matthew C. [1 ]
Barnes, Josephine [1 ]
Nielsen, Casper [1 ]
Kim, Lois G. [1 ,2 ]
Clegg, Shona L. [1 ]
Blair, Melanie [1 ]
Leung, Kelvin K. [1 ,3 ]
Douiri, Abdel [1 ]
Boyes, Richard G. [1 ]
Ourselin, Sebastien [1 ,3 ]
Fox, Nick C. [1 ]
机构
[1] UCL Inst Neurol, Dementia Res Ctr, London WC1N 3BG, England
[2] London Sch Hyg & Trop Med, London WC1, England
[3] UCL, Ctr Med Image Comp, London, England
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Alzheimer's disease; Mild cognitive impairment; MRI; Neuropsychology; Dementia; BRAIN ATROPHY; CEREBRAL ATROPHY; LONGITUDINAL MR; SERIAL MRI; RATES; PROGRESSION; REGISTRATION; DEMENTIA; DECLINE;
D O I
10.1007/s00330-009-1581-5
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
To assess the relationship between MRI-derived changes in whole-brain and ventricular volume with change in cognitive scores in Alzheimer's disease (AD), mild cognitive impairment (MCI) and control subjects. In total 131 control, 231 MCI and 99 AD subjects from the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort with T1-weighted volumetric MRIs from baseline and 12-month follow-up were used to derive volume changes. Mini mental state examination (MMSE), Alzheimer's disease assessment scale (ADAS)-cog and trails test changes were calculated over the same period. Brain atrophy rates and ventricular enlargement differed between subject groups (p < 0.0005) and in MCI and AD were associated with MMSE changes. Both measures were additionally associated with ADAS-cog and trails-B in MCI patients, and ventricular expansion was associated with ADAS-cog in AD patients. Brain atrophy (p < 0.0005) and ventricular expansion rates (p = 0.001) were higher in MCI subjects who progressed to AD within 12 months of follow-up compared with MCI subjects who remained stable. MCI subjects who progressed to AD within 12 months had similar atrophy rates to AD subjects. Whole-brain atrophy rates and ventricular enlargement differed between patient groups and healthy controls, and tracked disease progression and psychological decline, demonstrating their relevance as biomarkers.
引用
收藏
页码:674 / 682
页数:9
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