Gray matter atrophy rate as a marker of disease progression in AD

被引:63
作者
Anderson, Valerie M. [1 ]
Schott, Jonathan M. [2 ]
Bartlett, Jonathan W. [2 ,3 ]
Leung, Kelvin K. [2 ]
Miller, David H. [1 ]
Fox, Nick C. [2 ]
机构
[1] UCL Inst Neurol, Dept Neuroinflammat, London WC1N 3BG, England
[2] UCL Inst Neurol, Dementia Res Ctr, London WC1N 3BG, England
[3] London Sch Hyg & Trop Med, Dept Med Stat, London WC1, England
基金
英国医学研究理事会; 英国工程与自然科学研究理事会;
关键词
Gray matter; Atrophy rate; Alzheimer's disease; Sample sizes; MRI; MILD COGNITIVE IMPAIRMENT; TENSOR-BASED MORPHOMETRY; REMITTING MULTIPLE-SCLEROSIS; LONGITUDINAL BRAIN CHANGE; REGISTERED SERIAL MRI; ALZHEIMERS-DISEASE; CEREBRAL VOLUME; SAMPLE-SIZE; REGISTRATION; SEGMENTATION;
D O I
10.1016/j.neurobiolaging.2010.11.001
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Global gray matter (GM) atrophy rates were quantified from magnetic resonance imaging (MRI) over 6- and 12-month intervals in 37 patients with Alzheimer's disease (AD) and 19 controls using: (1) nonlinear registration and integration of Jacobian values, and (2) segmentation and subtraction of serial GM volumes. Sample sizes required to power treatment trials using global GM atrophy rate as an outcome measure were estimated and compared between the 2 techniques, and to global brain atrophy measures quantified using the boundary shift integral (brain boundary shift integral; BBSI) and structural image evaluation, using normalization, of atrophy (SIENA). Increased GM atrophy rates (approximately 2% per year) were observed in patients compared with controls. Although mean atrophy rates provided by Jacobian integration were smaller than those from segmentation and subtraction of GM volumes, measurement variance was reduced. The number of patients required per treatment arm to detect a 20% reduction in GM atrophy rate over a 12-month follow-up (90% power) was 202 (95% confidence interval [CI], 118-423) using Jacobian integration and 2047 (95% CI 271 to > 10 000) using segmentation and subtraction. Comparable sample sizes for whole brain atrophy were 240 (95% CI, 142-469) using the BBSI and 196 (95% CI, 110-425) using SIENA. Jacobian integration could be useful for measuring GM atrophy rate in Alzheimer's disease as a marker of disease progression and treatment efficacy. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1194 / 1202
页数:9
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