Statistical aspects of quantitative image analysis of β-amyloid in the APPV717F transgenic mouse model of Alzheimer's disease

被引:12
作者
Fishman, CE
Cummins, DJ
Bales, KR
DeLong, CA
Esterman, MA
Hanson, JC
White, SL
Paul, SM
Jordan, WH
机构
[1] Lilly Res Labs, Div Toxicol Pathol, Greenfield, IN 46140 USA
[2] Lilly Res Labs, Div Stat & Math Sci, Indianapolis, IN 46285 USA
[3] Purdue Univ, Sch Vet Med, Dept Vet Pathobiol, W Lafayette, IN 47907 USA
[4] Lilly Res Labs, Div Neurosci, Indianapolis, IN 46285 USA
[5] Lilly Res Labs, Div Informat Technol Discovery, Indianapolis, IN 46285 USA
关键词
Alzheimer's disease; animal model; beta-amyloid; histopathology; image analysis; mouse; power analysis; quantitative;
D O I
10.1016/S0165-0270(01)00381-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cerebral beta -amyloidosis is a central part of the neuropathology of Alzheimer's disease (AD). Quantitation of beta -amyloid plaques in the human AD brain, and in animal models of AD, is an important study endpoint in AD research. Methodologic approaches to the measurement of beta -amyloid in the brain vary between investigators, and these differences affect outcome measures. Here, one quantitative approach to the measurement of beta -amyloid plaques in brain sections was analyzed for sources of variability due to sampling. Brain tissue was from homozygous APP(V717F) transgenic male mice. Sampling variables were at the mouse and microscopic slide and field levels. Results indicated that phenotypic variability in the mouse sample population was the largest contributor to the standard error of the analyses. Within each mouse, variability between slides or between fields within slides had smaller effects on the error of the analyses. Therefore, when designing studies of adequate power, in this and in other similar models of cerebral beta -amyloidosis, sufficient numbers of mice per group must be included in order for change in mean plaque burden attributable to an experimental variable to outweigh phenotypic variability. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 152
页数:8
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