CORE 3 - CLINICAL TRANSLATIONAL RESEARCH CORE (CTRC): ABSTRACT The objective of the Clinical Translational Research Core (CTRC) is to facilitate high-quality clinical translational research specifically applicable to the understanding, prevention and treatment of diabetes, its complications, and related metabolic disorders. Research supported by the CTRC will leverage use of core facilities and faculty with expertise in a broad range in clinical research methods, from proof of concept and physiology, to clinical trials or comparative effectiveness studies to support the more than 35 Principal Investigators doing clinical research at Joslin. The CTRC will support the bi-directional journey of discovery from molecule, to model, to man, and back, while serving as the bridge between clinical observation, bench, and human investigation in adult and pediatric patients. Joslin has invested in new facilities for the Clinical Research Center which will serve as the infrastructure for the new DRC core. These facilities include exercise training and testing capacities, infusion and procedure rooms for adult and pediatric volunteers, and laboratory processing and biobanking facilities for valuable human specimens. We have well-trained nursing and technical staff to perform gold standard euglycemic, hyperglycemic, and hypoglycemic clamps at physiologic or pharmacologic insulin concentrations; intravenous and oral glucose and mixed meal tolerance tests; and other metabolic testing to assess insulin secretion, insulin action, and other metabolic processes for patient centered research specific to diabetes.
Specific aims of the new core are to 1) enable proof-of-concept and first-in-man ?T1? translational research programs with specific focus on Prediction, Prevention, and Interdiction of type 1 (T1DM) and type 2 diabetes (T2DM) and related complications; 2) facilitate design, implementation, and evaluation of investigator-initiated clinical trials and observational studies for translation to patients in ?T2-T3? research programs focused on improving and optimizing treatments of T1DM or T2DM and related complications; and 3) generate and maintain a registry of and a diabetes-specific biorepository of samples from our unique Joslin cohorts of patients with unusual phenotypes that have been extensively characterized. To achieve these aims the CTRC will provide an integrated and efficient core to support collaborative, multidisciplinary diabetes clinical research with services that include: a) consultation services, training, and mentoring of Investigators and fellows in methods and regulatory processes specific to human investigation; b) expert professional and technical help in the development and execution of protocols specific to diabetes and the complex assessments of glycemia, insulin secretion, insulin action, and exercise; c) support for biospecimen samples and data management; and d) guidance for analysis and interpretation of data and findings. Training will be an important component of the core supporting fellows and both new and established investigators. Together, these new initiatives will facilitate the translation of seminal observations and discoveries (which may begin at bench or bedside) into new diabetes cures or therapeutic opportunities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK036836-34
Application #
9921396
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
34
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215
Mulla, Christopher M; Middelbeek, Roeland J W; Patti, Mary-Elizabeth (2018) Mechanisms of weight loss and improved metabolism following bariatric surgery. Ann N Y Acad Sci 1411:53-64
Skupien, Jan; Smiles, Adam M; Valo, Erkka et al. (2018) Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced Nephropathy. Diabetes Care :
Laffel, L (2018) Lost in transition: finding a path forward for young adults with Type 1 diabetes. Diabet Med 35:1061-1062
Rao, Tata Nageswara; Gupta, Manoj K; Softic, Samir et al. (2018) Attenuation of PKC? enhances metabolic activity and promotes expansion of blood progenitors. EMBO J 37:
Bauman, Viviana; Sturkey, Adaya C; Sherafat-Kazemzadeh, Rosa et al. (2018) Factitious hypoglycemia in children and adolescents with diabetes. Pediatr Diabetes 19:823-831
Stanford, Kristin I; Rasmussen, Morten; Baer, Lisa A et al. (2018) Paternal Exercise Improves Glucose Metabolism in Adult Offspring. Diabetes 67:2530-2540
Park, Kyoungmin; Li, Qian; Evcimen, Net Da? et al. (2018) Exogenous Insulin Infusion Can Decrease Atherosclerosis in Diabetic Rodents by Improving Lipids, Inflammation, and Endothelial Function. Arterioscler Thromb Vasc Biol 38:92-101
Lynes, Matthew D; Shamsi, Farnaz; Sustarsic, Elahu Gosney et al. (2018) Cold-Activated Lipid Dynamics in Adipose Tissue Highlights a Role for Cardiolipin in Thermogenic Metabolism. Cell Rep 24:781-790
Schuster, Cornelia; Jonas, Franziska; Zhao, Fangzhu et al. (2018) Peripherally induced regulatory T cells contribute to the control of autoimmune diabetes in the NOD mouse model. Eur J Immunol 48:1211-1216
Laguna Sanz, Alejandro J; Mulla, Christopher M; Fowler, Kristen M et al. (2018) Design and Clinical Evaluation of a Novel Low-Glucose Prediction Algorithm with Mini-Dose Stable Glucagon Delivery in Post-Bariatric Hypoglycemia. Diabetes Technol Ther 20:127-139

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