The CNRU of Maryland will focus on the influence of nutrition and exercise on risk for age-related chronic diseases, including obesity, type 2 diabetes, hypertension, cardiovascular disease (CVD), sleep disordered breathing, and osteoporosis. With the obesity epidemic, associated co-morbidities now detract from the quality of life for the majority of Americans and represent a major burden to our health care system. Our research base brings together 44 investigators working on nutrition-related research at three institutions (University of Maryland, Johns Hopkins University, and U.S. Department of Agriculture, Beltsville), with multidisciplinary expertise and a strong track record of collaboration and NIH funding. To identify and evaluate the important genes that predict biological responses to diet (nutrigenomics) and exercise, our multidisciplinary research team utilizes the full spectrum of human genetics research from recruitment and phenotyping to high throughput molecular genetics to state-of-the-art statistical genetic analyses. Our team also has extensive experience in clinical and translational research, testing diet and exercise interventions to treat central obesity and the metabolic syndrome. Bridging genetics and clinical and translational research, a critical mass of investigators conduct basic research into the mechanisms regulating adipose tissue function. A cross-cutting theme of many research collaborations is understanding the genetic and nutritional contributors to high prevalence of obesity and its co-morbidities in minority populations, particularly African-Americans. Additionally, researchers address the genetic and environmental control of bone density and stroke risk and translational research to examine genetic and nutritional factors that increase risk of, and recovery from, hip fracture and stroke. The proposed Maryland CNRU will provide infrastructure and resources to expand the scope of our collaborative research efforts and to expedite new discoveries in nutrition-related research. The CNRU is organized into (Genetics;Interventions;Adipocyte Biology), (Genetics, Functional Genomics and Genetic Epidemiology;Clinical Research;Adipose Biology and Basic Mechanisms). We will also organize seminars, journal clubs, symposiums and other activities. The CNRU of Maryland will foster and facilitate research into critical issues in human nutrition and translate knowledge into effective therapies and interventions that address important health disparities in our population

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
3P30DK072488-05S1
Application #
7922345
Study Section
Special Emphasis Panel (ZDK1-GRB-1 (M2))
Program Officer
Miles, Carolyn
Project Start
2005-09-15
Project End
2010-08-31
Budget Start
2009-09-05
Budget End
2010-08-31
Support Year
5
Fiscal Year
2009
Total Cost
$126,500
Indirect Cost
Name
University of Maryland Baltimore
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Lent, Michelle R; Benotti, Peter N; Wood, G Craig (2018) Response to comment on Lent et al. All-Cause and Specific-Cause Mortality Risk After Roux-en-Y Gastric Bypass in Patients With and Without Diabetes. Diabetes Care 2017;40:1379-1385. Diabetes Care 41:e20
Spanakis, Elias K; Levitt, David L; Siddiqui, Tariq et al. (2018) The Effect of Continuous Glucose Monitoring in Preventing Inpatient Hypoglycemia in General Wards: The Glucose Telemetry System. J Diabetes Sci Technol 12:20-25
Montasser, May E; O'Hare, Elizabeth A; Wang, Xiaochun et al. (2018) An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels. Circulation 138:1343-1355
Taylor, Simeon I (2018) GLP-1 receptor agonists: differentiation within the class. Lancet Diabetes Endocrinol 6:83-85
Blau, Jenny E; Bauman, Viviana; Conway, Ellen M et al. (2018) Canagliflozin triggers the FGF23/1,25-dihydroxyvitamin D/PTH axis in healthy volunteers in a randomized crossover study. JCI Insight 3:
Geng, Xin; Irvin, Marguerite R; Hidalgo, Bertha et al. (2018) An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort. J Lipid Res 59:722-729
Ryan, Alice S; Serra, Monica C; Goldberg, Andrew P (2018) Metabolic Benefits of Prior Weight Loss with and without Exercise on Subsequent 6-Month Weight Regain. Obesity (Silver Spring) 26:37-44
Mitchell, Braxton D; Kalra, Gurmannat; Ryan, Kathleen A et al. (2018) Increased usual physical activity is associated with a blunting of the triglyceride response to a high-fat meal. J Clin Lipidol :
Differding, Moira K; Mueller, Noel T (2018) Are household disinfectants microbially mediated obesogens? CMAJ 190:E1095-E1096
Blau, Jenny E; Taylor, Simeon I (2018) Adverse effects of SGLT2 inhibitors on bone health. Nat Rev Nephrol 14:473-474

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