The objectives of the Biometrics and Statistical Development Core are first to provide statistical support for all of the projects in the Program, and second to advance the frontiers of methodology available for the analysis of repeated measures and particularly longitudinal data. This research is of major importance in optimizing the analysis of longitudinal data from aged and grafted animals. Both the statistical support roll and the methodological research roll of the Biometrics and Statistical Development Core serve the educational development of graduate students in Biometrics. Statistical support includes assistance in study design and appropriate sample size determination, data base management, summarizing, plotting, and analyzing data, and assistance in writing scientific papers and abstracts. Data analysis often involves estimating and comparing linear and nonlinear models fit to data collected repeatedly over time or dose on the same animals. This requires the use of advanced parametric and nonparametric analysis of variance techniques with which the Statistical Core is familiar, but which are not fully developed. This core's research effort will be focused on two areas. The first is to combine univariate nonlinear random effects models of the type discussed by Lindstrom and Bates (1990) with multivariate linear random effects models introduced by Zucker et al. (1995) in order to derive a multivariate nonlinear random effects model capable of simultaneously estimating, comparing and correlating the growth rates and half lives of several nonlinear growth or decay curves. The second is nonparametric, requiring no distribution assumptions. It is to develop a general linear model for longitudinal growth or time response curves based on randomization which encompasses a broad class of experimental designs and unifies inferences based on randomization as the standard general linear model does for inferences based on normal theory, and to apply this model to the problem of nonparametrically comparing growth curves after adjusting for covariates and possible informative censorship. The research topics posed above are ripe for significant progress and of importance to many of the Center's projects.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG004418-16
Application #
6097984
Study Section
Project Start
1999-04-01
Project End
2000-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
16
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Bickford, Paula C; Flowers, Antwoine; Grimmig, Bethany (2017) Aging leads to altered microglial function that reduces brain resiliency increasing vulnerability to neurodegenerative diseases. Exp Gerontol 94:4-8
Grimmig, Bethany; Kim, Seol-Hee; Nash, Kevin et al. (2017) Neuroprotective mechanisms of astaxanthin: a potential therapeutic role in preserving cognitive function in age and neurodegeneration. Geroscience 39:19-32
Tajiri, Naoki; Acosta, Sandra A; Shahaduzzaman, Md et al. (2014) Intravenous transplants of human adipose-derived stem cell protect the brain from traumatic brain injury-induced neurodegeneration and motor and cognitive impairments: cell graft biodistribution and soluble factors in young and aged rats. J Neurosci 34:313-26
Lee, Daniel C; Ruiz, Claudia R; Lebson, Lori et al. (2013) Aging enhances classical activation but mitigates alternative activation in the central nervous system. Neurobiol Aging 34:1610-20
Lee, D C; Rizer, J; Hunt, J B et al. (2013) Review: experimental manipulations of microglia in mouse models of Alzheimer's pathology: activation reduces amyloid but hastens tau pathology. Neuropathol Appl Neurobiol 39:69-85
Ross, Jaime M; Stewart, James B; Hagström, Erik et al. (2013) Germline mitochondrial DNA mutations aggravate ageing and can impair brain development. Nature 501:412-5
Shahaduzzaman, Md; Golden, Jason E; Green, Suzanne et al. (2013) A single administration of human umbilical cord blood T cells produces long-lasting effects in the aging hippocampus. Age (Dordr) 35:2071-87
Olson, Linus; Faulkner, Stuart; Lundströmer, Karin et al. (2013) Comparison of three hypothermic target temperatures for the treatment of hypoxic ischemia: mRNA level responses of eight genes in the piglet brain. Transl Stroke Res 4:248-57
Freeman, Linnea R; Granholm, Ann-Charlotte E (2012) Vascular changes in rat hippocampus following a high saturated fat and cholesterol diet. J Cereb Blood Flow Metab 32:643-53
Morganti, Josh M; Nash, Kevin R; Grimmig, Bethany A et al. (2012) The soluble isoform of CX3CL1 is necessary for neuroprotection in a mouse model of Parkinson's disease. J Neurosci 32:14592-601

Showing the most recent 10 out of 317 publications