The overall goal of the Pilot & Feasibility (P&F) Program is to facilitate new research development, and the career development of scientists, through pilot projects that synergize with the overall objectives of the DRC. Since our DRTC/DRC?s inception in 2008, the P&F program has been critical for growth in Center membership and extramural funding. Our P&F Program was instituted to tap growing interest in diabetes-related research at UAB and to foster development of junior faculty members, create partnerships, and take advantage of core resources. Our RFAs have attracted applications across the spectrum of translational research, yielding a diverse group of funded proposals ? including both clinical and basic research from both junior and senior investigators. To date, we have funded 55 diabetes-related pilot awards (out of 305 proposals submitted), 44% of which were clinical research projects and 65% of which were to junior investigators. Despite a reduced overall P&F Program budget awarded for the current cycle (2012-present), our program has remained vibrant, albeit with a 26% reduced number of awards funded per year and a 15% reduced average award size over this period. For the upcoming period, our specific aims are: 1) To identify and support new research projects of outstanding quality and innovation for pilot funding, ultimately resulting in substantial extramural support for developing these new lines of investigation; 2) To support promising junior faculty in career development through funding of outstanding pilots; 3) To augment the breadth and quality of DRC research by funding innovative projects of established researchers with valuable expertise who are new to diabetes, or of established diabetes investigators who want to test new high-impact hypotheses; and 4) To increase the number of independent investigators in the DRC funded by NIH for diabetes research. Our success is evidenced by the fact that nearly 70% of P&F awardees over the period of our DRTC/DRC program (2008 to present) has achieved substantial external funding for this research; this fraction is even greater (~83%) when we consider only the initial six years of the program. Greater than 90% of P&F awardees, including some not originally engaged in diabetes-related research, remain involved in diabetes investigation. This speaks to a growing intellectual climate and emphasis on diabetes at UAB and recognition that diabetes disproportionately affects the population served by our medical center. We will continue to capitalize on the strength of the UAB Interdisciplinary Research Centers (UWIRC) program, including the UAB Comprehensive Diabetes Center, and the supportive resources offered by the UAB Center for Clinical and Translational Research, our institutional CTSA. These connections, as well as vibrant clinical and basic science departments across the campus, will continue to propel our DRC P&F Program to greater success over the next cycle.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK079626-12
Application #
9771467
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
12
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Loomis, Stephanie J; Li, Man; Maruthur, Nisa M et al. (2018) Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results From the Atherosclerosis Risk in Communities Study. Diabetes 67:1684-1696
Wingo, Brooks C; Barry, Valene Garr; Ellis, Amy C et al. (2018) Comparison of segmental body composition estimated by bioelectrical impedance analysis and dual-energy X-ray absorptiometry. Clin Nutr ESPEN 28:141-147
Frugé, Andrew D; Cases, Mallory G; Howell, Carrie R et al. (2018) Fingernail and toenail clippings as a non-invasive measure of chronic cortisol levels in adult cancer survivors. Cancer Causes Control 29:185-191
Kim, Teayoun; Holleman, Cassie L; Nason, Shelly et al. (2018) Hepatic Glucagon Receptor Signaling Enhances Insulin-Stimulated Glucose Disposal in Rodents. Diabetes 67:2157-2166
Kreisler, A D; Mattock, M; Zorrilla, E P (2018) The duration of intermittent access to preferred sucrose-rich food affects binge-like intake, fat accumulation, and fasting glucose in male rats. Appetite 130:59-69
Sweatt, S Katherine; Gower, Barbara A; Chieh, Angela Y et al. (2018) Sleep quality is differentially related to adiposity in adults. Psychoneuroendocrinology 98:46-51
Chusyd, Daniella E; Brown, Janine L; Hambly, Catherine et al. (2018) Adiposity and Reproductive Cycling Status in Zoo African Elephants. Obesity (Silver Spring) 26:103-110
Ellis, Amy C; Hunter, Gary R; Goss, Amy M et al. (2018) Oral Supplementation with Beta-Hydroxy-Beta-Methylbutyrate, Arginine, and Glutamine Improves Lean Body Mass in Healthy Older Adults. J Diet Suppl :1-13
Bush, Nikki C; Resuehr, Holly E S; Goree, Laura Lee et al. (2018) A High-Fat Compared with a High-Carbohydrate Breakfast Enhances 24-Hour Fat Oxidation in Older Adults. J Nutr 148:220-226
Gupta, Rajesh; Nguyen, Dan C; Schaid, Michael D et al. (2018) Complement 1q-like-3 protein inhibits insulin secretion from pancreatic ?-cells via the cell adhesion G protein-coupled receptor BAI3. J Biol Chem 293:18086-18098

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