C. Abstract (Human Phenotyping) The Human Phenotyping Core (HPC) and its two sub-cores (the Energy Balance and Behavioral sub-cores) directly support the research of NORC members by providing innovative clinical and intervention services to phenotype humans in mechanistic, clinical, and translational studies. The services o f t h e Energy Balance sub-core include methods to quantify body composition, energy expenditure, carbohydrate metabolism, and cardiorespiratory fitness. The services of the Behavioral sub-core include behavioral, cognitive, and psychological assessments; measurement of food intake in laboratory and free-living conditions; design and delivery of behavioral change interventions; and assessment of activity and sedentary behavior in free- living conditions. Over the first 10 years of NORC funding, the HPC: a) provided comprehensive services for human phenotyping in clinical research studies, b) developed and validated innovative phenotyping methods and interventions, c) established quality control procedures, and d) built a growing base of HPC users. In years 1-5, the majority of the HPC's effort focused on adult phenotyping. Over years 6-10, however, the HPC transitioned to include g reater emphasis on novel imaging techniques and methods to phenotype mothers, infants, and children. This is consistent with the NORC's theme of nutrition, obesity, and metabolic health through the lifespan. At each period of the lifespan, we conduct research to understand the mechanisms, prevention, and treatment of obesity; and our research focus areas have evolved to include a) maternal and infant nutritional status, b) pediatric and adulthood obesity, and c) nutritional status in older age to preserve physical and cognitive functionality.
The Aims of the current renewal application to fund years 11-15 are: 1) provide members with a comprehensive suite of innovative energy balance and behavioral services to ongoing funded and collaborative research projects to enable the characterization of human subjects in clinical and translational research studies, and continue to expand services to phenotype individuals at specific stages of life, such as pregnancy and infancy, 2) provide specialist expertise to support clinical and translational research on nutrition, obesity and metabolic health at different stages of life, and continue to enhance our quality control procedures to provide efficient and high quality services, 3) sustain a human tissue bio-repository, including metabolic tissues (muscle, adipose) and biospecimens that are needed for ongoing fundamental and translational studies of nutrition, obesity, and metabolic health relative to pregnancy (placenta, cord blood), infancy (breast milk), and childhood, 4) expand imaging capabilities including food-intake-relevant fMRI, enhanced body composition and metabolism, and rodent imaging to increase the power and quality of our research results, and 5) proactively facilitate increased utilization of the core services; integrate core services with pilot and feasibility studies; and continually monitor and improve utilization and priorities for core services.
These aims build upon the previous 10 years of work and bolster support for NORC members' research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK072476-13
Application #
9475767
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2005-09-15
Project End
Budget Start
2018-05-01
Budget End
2019-04-30
Support Year
13
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Lsu Pennington Biomedical Research Center
Department
Type
DUNS #
611012324
City
Baton Rouge
State
LA
Country
United States
Zip Code
70808
Herion, Nils Janis; Kruger, Claudia; Staszkiewicz, Jaroslaw et al. (2018) Embryonic cell migratory capacity is impaired upon exposure to glucose in vivo and in vitro. Birth Defects Res :
Katzmarzyk, Peter T; Most, Jasper; Redman, Leanne M et al. (2018) Energy expenditure and substrate oxidation in White and African American young adults without obesity. Eur J Clin Nutr 72:920-922
Hsueh, Wen-Chi; Bennett, Peter H; Esparza-Romero, Julian et al. (2018) Analysis of type 2 diabetes and obesity genetic variants in Mexican Pima Indians: Marked allelic differentiation among Amerindians at HLA. Ann Hum Genet 82:287-299
Yu, Yongmei; Mendoza, Tamra M; Ribnicky, David M et al. (2018) An Extract of Russian Tarragon Prevents Obesity-Related Ectopic Lipid Accumulation. Mol Nutr Food Res 62:e1700856
Yan, Hao; Carmichael, Owen; Paul, Debashis et al. (2018) Estimating fiber orientation distribution from diffusion MRI with spherical needlets. Med Image Anal 46:57-72
Obanda, Diana; Page, Ryan; Guice, Justin et al. (2018) CD Obesity-Prone Rats, but not Obesity-Resistant Rats, Robustly Ferment Resistant Starch Without Increased Weight or Fat Accretion. Obesity (Silver Spring) 26:570-577
Wanders, Desiree; Forney, Laura A; Stone, Kirsten P et al. (2018) The Components of Age-Dependent Effects of Dietary Methionine Restriction on Energy Balance in Rats. Obesity (Silver Spring) 26:740-746
Trepanowski, John F; Kroeger, Cynthia M; Barnosky, Adrienne et al. (2018) Effects of alternate-day fasting or daily calorie restriction on body composition, fat distribution, and circulating adipokines: Secondary analysis of a randomized controlled trial. Clin Nutr 37:1871-1878
Staiano, Amanda E; Webster, Elizabeth Kipling; Allen, Andrew T et al. (2018) Screen-Time Policies and Practices in Early Care and Education Centers in Relationship to Child Physical Activity. Child Obes 14:341-348
Carmichael, Owen; Schwarz, Adam J; Chatham, Christopher H et al. (2018) The role of fMRI in drug development. Drug Discov Today 23:333-348

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