Age-related changes in grey and white matter structure throughout adulthood

被引:379
作者
Giorgio, Antonio [1 ,2 ]
Santelli, Luca [3 ]
Tomassini, Valentina [1 ]
Bosnell, Rose [1 ]
Smith, Steve [1 ]
De Stefano, Nicola [2 ]
Johansen-Berg, Heidi [1 ]
机构
[1] John Radcliffe Hosp, FMRIB Ctr, Oxford OX3 9DU, England
[2] Univ Siena, Dept Neurol & Behav Sci, Neurol & Neurometab Unit, I-53100 Siena, Italy
[3] Univ Padua, Sch Med, Dept Neurosci, Padua, Italy
基金
英国惠康基金; 英国工程与自然科学研究理事会;
关键词
QUANTITATIVE MAGNETIC-RESONANCE; VOXEL-BASED ANALYSIS; DIFFUSION-TENSOR; MULTIPLE-SCLEROSIS; CORPUS-CALLOSUM; CEREBRAL-CORTEX; GRAY-MATTER; IN-VIVO; DIFFERENTIAL VULNERABILITY; FRACTIONAL ANISOTROPY;
D O I
10.1016/j.neuroimage.2010.03.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Normal ageing is associated with gradual brain atrophy. Determining spatial and temporal patterns of change can help shed light on underlying mechanisms. Neuroimaging provides various measures of brain structure that can be used to assess such age-related change but studies to date have typically considered single imaging measures. Although there is consensus on the notion that brain structure deteriorates with age, evidence on the precise time course and spatial distribution of changes is mixed. We assessed grey matter (GM) and white matter (WM) structure in a group of 66 adults aged between 23 and 81. Multimodal imaging measures included voxel-based morphometry (VBM)-style analysis of GM and WM volume and diffusion tensor imaging (DTI) metrics of WM microstructure. We found widespread reductions in GM volume from middle age onwards but earlier reductions in GM were detected in frontal cortex. Widespread age-related deterioration in WM microstructure was detected from young adulthood onwards. WM decline was detected earlier and more sensitively using DTI-based measures of microstructure than using markers of WM volume derived from conventional T1-weighted imaging. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:943 / 951
页数:9
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