Diabetes is estimated to be the sixth leading cause of death in the U.S., and is found to occur disproportionately in minority populations. The prevalence of diabetes increased by ~ 50 % from 1990 to 2000, and is still on the rise. The estimated total national cost of diabetes in 2007 was $174 billion, the majority going directly to medical expenditures. Diabetes is responsible for 12,000 - 24,000 new cases of blindness each year, and is the leading cause of kidney failure, responsible for ~ 150,000 patients with end-stage kidney disease. It is also responsible for 60% of non-traumatic lower limb amputations - 82,000 in 2002 were due to diabetes. In response to this epidemic, there are currently more than 350 candidate drugs in development making diabetes second only to cancer in health related R&D focus. Concurrent with the need for better treatments, there is a recognized need to produce sets of improved biomarkers able to better assess efficacy, sub-type populations and to longitudinally monitor disease progression and response to treatment. Under this proposal, entitled """"""""Team Approach to Translate Novel Biomarkers for Diabetes"""""""", we will create a highly integrated, multidisciplinary research team specifically assembled to discover, validate and translate novel biomarkers for diabetes (and its complications) into improved commercial diagnostics. The envisioned biomarkers will better predict the onset of disease and define the optimal therapeutic or pharmaceutical interventions to significantly improve patient outcomes. During this initial seed period, we will assemble a unique and highly-experienced planning team consisting of technical, clinical, informatics, and translational experts, along with external industrial partners, to design programmatic investigations into protein biomarkers to address the critical needs in patient diagnosis and monitoring, and drug development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Resource-Related Research Projects (R24)
Project #
1R24DK083948-01
Application #
7694487
Study Section
Special Emphasis Panel (ZDK1-GRB-2 (M2))
Program Officer
Sechi, Salvatore
Project Start
2009-07-01
Project End
2011-06-30
Budget Start
2009-07-01
Budget End
2011-06-30
Support Year
1
Fiscal Year
2009
Total Cost
$466,729
Indirect Cost
Name
Arizona State University-Tempe Campus
Department
Miscellaneous
Type
Organized Research Units
DUNS #
943360412
City
Tempe
State
AZ
Country
United States
Zip Code
85287
Azizkhanian, Ida; Trenchevska, Olgica; Bashawri, Yara et al. (2016) Posttranslational modifications of apolipoprotein A-II proteoforms in type 2 diabetes. J Clin Lipidol 10:808-815
Kimzey, Michael J; Kinsky, Owen R; Yassine, Hussein N et al. (2015) Site specific modification of the human plasma proteome by methylglyoxal. Toxicol Appl Pharmacol 289:155-62
Monks, Terrence J; Lau, Serrine S (2013) Reactive intermediates: molecular and MS-based approaches to assess the functional significance of chemical-protein adducts. Toxicol Pathol 41:315-21
Yassine, Hussein; Borges, Chad R; Schaab, Matthew R et al. (2013) Mass spectrometric immunoassay and MRM as targeted MS-based quantitative approaches in biomarker development: potential applications to cardiovascular disease and diabetes. Proteomics Clin Appl 7:528-40
Borges, Chad R; Rehder, Douglas S; Boffetta, Paolo (2013) Multiplexed surrogate analysis of glycotransferase activity in whole biospecimens. Anal Chem 85:2927-36
Yassine, Hussein; Kimzey, Michael J; Galligan, Michael A et al. (2012) Adjusting for Urinary Creatinine Overestimates Arsenic Concentrations in Diabetics. Cardiorenal Med 2:26-32
Nelson, Randall W; Borges, Chad R (2011) Mass spectrometric immunoassay revisited. J Am Soc Mass Spectrom 22:960-8
Oran, Paul E; Jarvis, Jason W; Borges, Chad R et al. (2011) Mass spectrometric immunoassay of intact insulin and related variants for population proteomics studies. Proteomics Clin Appl 5:454-9
Kimzey, Michael J; Yassine, Hussein N; Riepel, Brent M et al. (2011) New site(s) of methylglyoxal-modified human serum albumin, identified by multiple reaction monitoring, alter warfarin binding and prostaglandin metabolism. Chem Biol Interact 192:122-8
Borges, Chad R; Oran, Paul E; Buddi, Sai et al. (2011) Building multidimensional biomarker views of type 2 diabetes on the basis of protein microheterogeneity. Clin Chem 57:719-28

Showing the most recent 10 out of 12 publications