Normative estimates of cross-sectional and longitudinal brain volume decline in aging and AD

被引:411
作者
Fotenos, AF
Snyder, AZ
Girton, LE
Morris, JC
Buckner, RL
机构
[1] Washington Univ, Howard Hughes Med Inst, Dept Neurol, Mallinckrodt Inst Radiol,Div Biol & Biomed Sci, St Louis, MO 63108 USA
[2] Washington Univ, Dept Psychol, St Louis, MO 63108 USA
关键词
D O I
10.1212/01.WNL.0000154530.72969.11
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To test the hypotheses 1) that whole-brain volume decline begins in early adulthood, 2) that cross-sectional and longitudinal atrophy estimates agree in older, nondemented individuals, and 3) that longitudinal atrophy accelerates in the earliest stages of Alzheimer disease ( AD). Methods: High-resolution, high-contrast structural MRIs were obtained from 370 adults ( age 18 to 97). Participants over 65 ( n = 192) were characterized using the Clinical Dementia Rating ( CDR) as either nondemented ( CDR 0, n = 94) or with very mild to mild dementia of the Alzheimer type (DAT, CDR 0.5 and 1, n = 98). Of these older participants, 79 belonged to a longitudinal cohort and were imaged again a mean 1.8 years after baseline. Estimates of gray matter ( nGM), white matter ( nWM), and whole-brain volume ( nWBV) normalized for head sizes were generated based on atlas registration and image segmentation. Results: Hierarchical regression of nWBV estimates from nondemented individuals across the adult lifespan revealed a strong linear, moderate quadratic pattern of decline beginning in early adulthood, with later onset of nWM than nGM loss. Whole-brain volume differences were detected by age 30. The cross-sectional atrophy model overlapped with the rates measured longitudinally in older, nondemented individuals ( mean decline of -0.45% per year). In those individuals with very mild DAT, atrophy rate more than doubled ( -0.98% per year). Conclusions: Nondemented individuals exhibit a slow rate of whole- brain atrophy from early in adulthood with white- matter loss beginning in middle age; in older adults, the onset of dementia of the Alzheimer type is associated with a markedly accelerated atrophy rate.
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页码:1032 / 1039
页数:8
相关论文
共 60 条
[1]   Quadratic trajectories of brain myelin content: unifying construct for neuropsychiatric disorders [J].
Bartzokis, G .
NEUROBIOLOGY OF AGING, 2004, 25 (01) :49-62
[2]   Age-related myelin breakdown: a developmental model of cognitive decline and Alzheimer's disease [J].
Bartzokis, G .
NEUROBIOLOGY OF AGING, 2004, 25 (01) :5-18
[3]   Clinicopathologic studies in cognitively healthy aging and Alzheimer disease - Relation of histologic markers to dementia severity, age, sex, and apolipoprotein E genotype [J].
Berg, L ;
McKeel, DW ;
Miller, JP ;
Storandt, M ;
Rubin, EH ;
Morris, JC ;
Baty, J ;
Coats, M ;
Norton, J ;
Goate, AM ;
Price, JL ;
Gearing, M ;
Mirra, SS ;
Saunders, AM .
ARCHIVES OF NEUROLOGY, 1998, 55 (03) :326-335
[4]  
BLATTER DD, 1995, AM J NEURORADIOL, V16, P241
[5]   Frequency of stages of Alzheimer-related lesions in different age categories [J].
Braak, H ;
Braak, E .
NEUROBIOLOGY OF AGING, 1997, 18 (04) :351-357
[6]   A unified approach for morphometric and functional data analysis in young, old, and demented adults using automated atlas-based head size normalization: reliability and validation against manual measurement of total intracranial volume [J].
Buckner, RL ;
Head, D ;
Parker, J ;
Fotenos, AF ;
Marcus, D ;
Morris, JC ;
Snyder, AZ .
NEUROIMAGE, 2004, 23 (02) :724-738
[7]   Comparison of methods for measuring longitudinal brain change in cognitive impairment and dementia [J].
Cardenas, VA ;
Du, AT ;
Hardin, D ;
Ezekiel, F ;
Weber, P ;
Jagust, WJ ;
Chui, HC ;
Schuff, N ;
Weiner, MW .
NEUROBIOLOGY OF AGING, 2003, 24 (04) :537-544
[8]   Change in rates of cerebral atrophy over time in early-onset Alzheimer's disease: longitudinal MRI study [J].
Chan, D ;
Janssen, JC ;
Whitwell, JL ;
Watt, HC ;
Jenkins, R ;
Frost, C ;
Rossor, MN ;
Fox, NC .
LANCET, 2003, 362 (9390) :1121-1122
[9]   Rates of global and regional cerebral atrophy in AD and frontotemporal dementia [J].
Chan, D ;
Fox, NC ;
Jenkins, R ;
Scahill, RI ;
Crum, WR ;
Rossor, MN .
NEUROLOGY, 2001, 57 (10) :1756-1763
[10]  
CHRISTIANSEN P, 1994, ACTA RADIOL, V35, P117