The objectives of the Statistical 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 the same sheep or human subjects. Both the statistical support roll and the methodological research roll of the Statistical Core serve the educational development of pediatrics fellows and 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 subjects. 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 growth and rate parameters 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 possibly informative censorship. The research topics posed above are ripe for significant progress and of importance to many of the Program's projects.

Project Start
1999-07-01
Project End
2000-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
14
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
Regnault, Timothy R H; de Vrijer, Barbra; Galan, Henry L et al. (2013) Umbilical uptakes and transplacental concentration ratios of amino acids in severe fetal growth restriction. Pediatr Res 73:602-11
Manco-Johnson, Marilyn J; Hacker, Michele R; Jacobson, Linda J et al. (2009) Pharmacokinetics of protein C and antithrombin in the fetal lamb: a model to predict human neonatal replacement dosing. Neonatology 95:279-85
Wilkes, Paul T; Meschia, Giacomo; Teng, Cecilia et al. (2003) The effect of an elevated maternal lysine concentration on placental lysine transport in pregnant sheep. Am J Obstet Gynecol 189:1494-500
Timmerman, M; Wilkening, R B; Regnault, T R H (2003) Induction of glutamate dehydrogenase in the ovine fetal liver by dexamethasone infusion during late gestation. Exp Biol Med (Maywood) 228:100-5
Paolini, C L; Teng, C; Jozwik, M et al. (2003) Umbilical threonine uptake during maternal threonine infusion in sheep. Placenta 24:354-60
Ferrazzi, E; Bozzo, M; Rigano, S et al. (2002) Temporal sequence of abnormal Doppler changes in the peripheral and central circulatory systems of the severely growth-restricted fetus. Ultrasound Obstet Gynecol 19:140-6
Teng, Cecilia C; Tjoa, Susan; Fennessey, Paul V et al. (2002) Transplacental carbohydrate and sugar alcohol concentrations and their uptakes in ovine pregnancy. Exp Biol Med (Maywood) 227:189-95
Teng, Cecilia; Battaglia, Frederick C; Meschia, Giacomo et al. (2002) Fetal hepatic and umbilical uptakes of glucogenic substrates during a glucagon-somatostatin infusion. Am J Physiol Endocrinol Metab 282:E542-50
Regnault, T R H; Orbus, R J; de Vrijer, B et al. (2002) Placental expression of VEGF, PlGF and their receptors in a model of placental insufficiency-intrauterine growth restriction (PI-IUGR). Placenta 23:132-44
Paolini, C L; Marconi, A M; Pike, A W et al. (2001) A multiple infusion start time (MIST) protocol for stable isotope studies of fetal blood. Placenta 22:171-6

Showing the most recent 10 out of 24 publications