The Boston Obesity Nutrition Center (BNORC) was founded in 1992 and has been administratively based at Boston Medical Center (BMC) for the past 20 years. The BNORC consortium is a collaboration consisting of Boston University School of Medicine, Tufts University, Beth Israel Deaconess Medical Center and Harvard School of Public Health and serves nutrition and obesity scientists in the greater Boston area. The overall objective of BNORC is to 1) facilitate and support the conduct of cutting edge basic, translational and clinical research in the fields of nutrition and obesity science, and 2) provide resources and educational opportunities that enrich the training of new investigators and promote multi- and interdisciplinary research collaborations. Five Cores serve these goals: A) Administrative (B. E. Corkey, Director, G. Blackburn and C. Apovian, Clinical Associate Directors and A. S. Greenberg, Pilot and Feasibility Associate Director), B) Adipose Biology and Nutrient Metabolism (B. E. Corkey and S. R. Farmer, Co-Directors), C) Epidemiology and Genetics (F. Hu and J. Chavarro, Directors), D) Functional Genomics and Bioinformatics (E. Rosen, Director, and L. Tsai, Associate Director), and E) Transgenic (B. Lowell, Director). The BNORC research base includes 123 members with $49 million of nutrition- and obesity-related federal funding ($13,709,527 (29%) NIDDK and 71% other federal or national). These scientists address basic, clinical and population aspects of three interrelated themes: 1) Nutrient Metabolism in Health and Disease; 2) Brain Control of Feeding Behavior and Metabolism; and 3) Environment and Genetic Influences on Obesity and Related Chronic Diseases. In the past funding period our basic research Cores have evolved to better support the research needs of basic scientists who need state-of- the-art tools to evaluate genetic, genomic, epigenetic, transcriptomic, and functional genomic approaches to understand the biological underpinning that drive food intake and metabolism and how these become dysfunctional in obesity. The Epidemiology and Genetics core provides members who conduct epidemiological and clinical research, as well as basic researchers seeking to translate their findings, with access to large dataset to assess lifestyle (diet, physical activity) and genetic contributions to the development of obesity and related diseases. Core support high impact research by our members and fosters collaborative efforts. Substantial resources are dedicated to our Pilot and Feasibility Program that continues to support the early independent careers of many prominent scientists in the field.

Public Health Relevance

Obesity is a major health problem in the United States. Obesity increases risk for metabolic disease such as type 2 diabetes and shortens lifespan. The Boston Nutrition Obesity Research Center brings together nutrition researchers across Boston who study cells, patients with obesity and populations to understand the biology of obesity with the long-term goal of developing new treatments. We focus on how the brain controls food intake, on dietary and lifestyle factors that affect body weight and on how obesity affects the way the body uses nutrients. The Center provides access to state-of-the art technologies to efficiently carry out this work, and provides new investigators with opportunities for winning small pilot funding to develop their careers and ideas.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK046200-28
Application #
9936143
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Evans, Mary
Project Start
1997-09-30
Project End
2022-05-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
28
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Boston Medical Center
Department
Type
DUNS #
005492160
City
Boston
State
MA
Country
United States
Zip Code
02118
Killion, Elizabeth A; Reeves, Andrew R; El Azzouny, Mahmoud A et al. (2018) A role for long-chain acyl-CoA synthetase-4 (ACSL4) in diet-induced phospholipid remodeling and obesity-associated adipocyte dysfunction. Mol Metab 9:43-56
Leitner, Brooks P; Weiner, Lauren S; Desir, Matthew et al. (2018) Kinetics of human brown adipose tissue activation and deactivation. Int J Obes (Lond) :
Gaskins, Audrey J; Rich-Edwards, Janet W; Williams, Paige L et al. (2018) Pre-pregnancy caffeine and caffeinated beverage intake and risk of spontaneous abortion. Eur J Nutr 57:107-117
Hansen, S; Halldorsson, T I; Olsen, S F et al. (2018) Birth by cesarean section in relation to adult offspring overweight and biomarkers of cardiometabolic risk. Int J Obes (Lond) 42:15-19
Maldonado-Cárceles, Ana B; Mínguez-Alarcón, Lidia; Mendiola, Jaime et al. (2018) Meat intake in relation to semen quality and reproductive hormone levels among young men in Spain. Br J Nutr :1-10
Han, Liyuan; Duan, Donghui; Zhang, Shuang et al. (2018) Effects of the interaction between glycated haemoglobin genetic risk score and postpartum weight reduction on glycaemic changes: A gene-weight interaction analysis. Diabetes Obes Metab 20:2733-2739
Jager, Mike; Lee, Mi-Jeong; Li, Chendi et al. (2018) Aortic carboxypeptidase-like protein enhances adipose tissue stromal progenitor differentiation into myofibroblasts and is upregulated in fibrotic white adipose tissue. PLoS One 13:e0197777
Cardamone, Maria Dafne; Tanasa, Bogdan; Cederquist, Carly T et al. (2018) Mitochondrial Retrograde Signaling in Mammals Is Mediated by the Transcriptional Cofactor GPS2 via Direct Mitochondria-to-Nucleus Translocation. Mol Cell 69:757-772.e7
Martin Carli, Jayne F; LeDuc, Charles A; Zhang, Yiying et al. (2018) FTO mediates cell-autonomous effects on adipogenesis and adipocyte lipid content by regulating gene expression via 6mA DNA modifications. J Lipid Res 59:1446-1460
Buendia, Justin R; Li, Yanping; Hu, Frank B et al. (2018) Regular Yogurt Intake and Risk of Cardiovascular Disease Among Hypertensive Adults. Am J Hypertens 31:557-565

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