We propose to develop new statistical methods for improving analyses of multivariate, longitudinal and functional data from biomedical studies. There is increasing concern that exposures occurring during critical windows can lead to later adverse health effects, motivating prospective studies collecting detailed data on multiple time-varying exposures and health outcomes. New statistical methods are needed to efficiently discover critical windows and time-varying dependencies in such high-dimensional data sets, while limiting false discoveries. These methods may lead to fundamental new insights into mechanisms by which exposures induce adverse health effects, while also allowing for the development of targeted interventions and more accurate predictions of disease risk. Our goals include the following. 1. Develop nonparametric Bayes statistical methods for flexibly characterizing differences among individuals in functional data, such as trajectories over time in oxidative stress, reproductive hormones, nutrients and pregnancy weight. 2. Develop methods for flexibly predicting a health response based on multiple time- varying factors, while also estimating critical windows and discovering dynamic relationships between the different factors. 3. Apply these methods to assess relationships between oxidative stress, nutrients and reproductive hormones over the menstrual cycle accounting for the role of age, obesity and smoking. Also consider applications to identify patterns of pregnancy weight gain associated with short-term infant health outcomes.

Public Health Relevance

The development of adverse health conditions, such as infertility and diabetes, depends on the interaction between genetic predisposition and a variety of lifestyle factors, including diet and environmental exposures. Changes with age in these factors is an important determinate of risk, as critical windows can occur many years before disease onset. We provide the statistical tools necessary to identify critical windows of exposure in order to reduce risk through targeted interventions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
1R01ES017240-01
Application #
7628797
Study Section
Biostatistical Methods and Research Design Study Section (BMRD)
Program Officer
Dilworth, Caroline H
Project Start
2009-05-15
Project End
2014-03-31
Budget Start
2009-05-15
Budget End
2010-03-31
Support Year
1
Fiscal Year
2009
Total Cost
$280,800
Indirect Cost
Name
Duke University
Department
Biostatistics & Other Math Sci
Type
Schools of Arts and Sciences
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
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