This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.OBJECTIVE: The objectives are to establish the magnitude of the epidemic of NAFLD in T2DM (protocol #1 or 'Screening Study') and to compare the current standard of care (dietary intervention alone) vs. the insulin-sensitizer pioglitazone (protocol #2 or 'Treatment of NAFLD Study'). We want to establish if pioglitazone is a disease-modifying agent for patients with T2DM and NAFLD/NASH.RESEARCH PLAN: Type 2 diabetes mellitus (T2DM) is a major public health problem, but less well recognized is that obesity and T2DM are fueling another 'silent epidemic': nonalcoholic fatty liver disease (NAFLD). NAFLD is a chronic liver condition associated with insulin resistance, impaired glucose intolerance or frank type 2 diabetes (T2DM) and hepatic fat accumulation, ranging from simple steatosis to severe steatohepatitis with necroinflammation (NASH) and eventually fibrosis. The diagnosis of NAFLD and NASH is difficult as it gives few symptoms, the most common being vague right upper quadrant discomfort, and while liver enzymes may be elevated (ALTAST) in NAFLD, the real problem is that they are normal in ~2/3 of patients. Therefore, a large number of patients are undiagnosed and undergoing chronic liver damage.METHODS: There are two steps in this proposal. The first is to establish the magnitude of the epidemic of NAFLD in T2DM (protocol #1 or 'Screening Study'). To this end, we plan to screen 250 unselected patients with T2DM for NAFLD from the San Antonio area non-invasively by magnetic resonance spectroscopy (MRS) which is the gold-standard technique.
The second aim as outlined in protocol #2 ('Treatment of NAFLD Study') will be to estimate the incidence of NASH (hepatic fat accumulation plus necroinflammation and/or fibrosis by liver biopsy - the only way to establish this diagnosis as it cannot be done by imaging) and compare two treatments: the current standard of care (the empiric approach based on dietary intervention alone) vs. the insulin-sensitizer pioglitazone. This will allow us to establish if pioglitazone is a disease-modifying agent during long-term treatment, capable of changing the natural history of NAFLD/NASH in patients with T2DM.CLINICAL

Public Health Relevance

There are no large studies to date as the one proposed here to bridge the gap in our knowledge about the real magnitude of the epidemic of fatty liver disease in T2DM. The greater availability of MRS has allowed a fast and highly reproducible way to measure liver fat. In our experience with MRS over the past five years, we have established that ~80% of patients with T2DM have NAFLD and Hispanics had a greater hepatic fat content when matched for major pertinent variables (unpublished). Recent studies have confirmed that Hispanics are at much greater risk of NAFLD than Caucasians or African-Americans, making this proposal particularly relevant for the San Antonio community in order to develop new prevention and early intervention strategies.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR001346-27
Application #
7718702
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2008-04-01
Project End
2008-05-31
Budget Start
2008-04-01
Budget End
2008-05-31
Support Year
27
Fiscal Year
2008
Total Cost
$2,489
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Kawaguchi-Suzuki, Marina; Cusi, Kenneth; Bril, Fernando et al. (2018) A Genetic Score Associates With Pioglitazone Response in Patients With Non-alcoholic Steatohepatitis. Front Pharmacol 9:752
Hayden, Kathleen M; Baker, Laura D; Bray, George et al. (2018) Long-term impact of intensive lifestyle intervention on cognitive function assessed with the National Institutes of Health Toolbox: The Look AHEAD study. Alzheimers Dement (Amst) 10:41-48
Unick, Jessica L; Gaussoin, Sarah A; Hill, James O et al. (2017) Objectively Assessed Physical Activity and Weight Loss Maintenance among Individuals Enrolled in a Lifestyle Intervention. Obesity (Silver Spring) 25:1903-1909
Kawaguchi-Suzuki, M; Bril, F; Kalavalapalli, S et al. (2017) Concentration-dependent response to pioglitazone in nonalcoholic steatohepatitis. Aliment Pharmacol Ther 46:56-61
Johnson, Karen C; Bray, George A; Cheskin, Lawrence J et al. (2017) The Effect of Intentional Weight Loss on Fracture Risk in Persons With Diabetes: Results From the Look AHEAD Randomized Clinical Trial. J Bone Miner Res 32:2278-2287
Lorenzo, Carlos; Festa, Andreas; Hanley, Anthony J et al. (2017) Novel Protein Glycan-Derived Markers of Systemic Inflammation and C-Reactive Protein in Relation to Glycemia, Insulin Resistance, and Insulin Secretion. Diabetes Care 40:375-382
Beavers, Kristen M; Leng, Iris; Rapp, Stephen R et al. (2017) Effects of Longitudinal Glucose Exposure on Cognitive and Physical Function: Results from the Action for Health in Diabetes Movement and Memory Study. J Am Geriatr Soc 65:137-145
Chao, Ariana M; Wadden, Thomas A; Gorin, Amy A et al. (2017) Binge Eating and Weight Loss Outcomes in Individuals with Type 2 Diabetes: 4-Year Results from the Look AHEAD Study. Obesity (Silver Spring) 25:1830-1837
Williams, Robert C; Elston, Robert C; Kumar, Pankaj et al. (2016) Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND). BMC Genomics 17:325
Belalcazar, L Maria; Papandonatos, George D; Erar, Bahar et al. (2016) Lifestyle Intervention for Weight Loss and Cardiometabolic Changes in the Setting of Glucokinase Regulatory Protein Inhibition: Glucokinase Regulatory Protein-Leu446Pro Variant in Look AHEAD. Circ Cardiovasc Genet 9:71-8

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