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.Insulin resistance and diabetes are the source of considerable health and financial burden for our older adult population. Recent estimates show that the direct medical costs of diabetes and its related disorders climbed from $44 billion in 1997 to almost $92 billion in 2002. Consequently, the search for effective treatment or prevention modalities is a high priority in public health care policy. Although diet and exercise improve insulin sensitivity, it is still entirely unclear as to what regimen of diet composition and exercise is most effective in reversing insulin resistance in older adults. The proposed research will involve the prospective study of 80 older (60-80 years) men and women. The central hypothesis is that a low-glycemic diet, combined with aerobic exercise and nutrition counseling reduces insulin resistance in older men and women.
The specific aims are, I: Identify the effects of high- and low-glycemic diet and exercise interventions on insulin resistance in older adults. II: Ascertain which components of body composition are regulated by high- and low-glycemic diet-exercise interventions. III: Establish which insulin signaling proteins in skeletal muscle regulate the change in insulin resistance in response to high- and low-glycemic diet-exercise interventions. The approach includes a 3-week diet/weight stabilization period during which all subjects will be fed a weight-maintenance typical American diet. Subjects will be randomized to receive either a eucaloric high-glycemic diet (~90 U), or a eucaloric low-glycemic diet (~55 U). All meals will be prepared in the General Clinical Research Center Metabolic Kitchen. Subjects will participate in an acute (7-day) and/or chronic (12-week) supervised aerobic exercise program and nutrition counseling. Baseline physiological and metabolic testing will include measures of insulin resistance (euglycemic-hyperinsulinemic clamps), substrate oxidation, total and abdominal fat (computer tomography), lipids, and cytokines. Muscle biopsies will be obtained to measure expression, phosphorylation and activity of proteins in the insulin-signaling pathway. Myocellular lipid content will be determined by proton-nuclear magnetic spectroscopy. Upon treatment completion, all subjects will remain on their respective diet, maintain weight stability and repeat all baseline testing to determine the study outcome effects. It is our expectation that the approach used in this study will identify a more favorable diet-exercise treatment for insulin resistance, as well as the cellular and metabolic mediators that regulate insulin resistance in older adults. These results will be significant, in that they will provide a preventative and therapeutic intervention that will substantially improve the health and quality of life for the growing number of older adults who have developed, or will develop insulin resistance, or diabetes.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR018390-05
Application #
7608222
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2007-04-01
Project End
2007-09-16
Budget Start
2007-04-01
Budget End
2007-09-16
Support Year
5
Fiscal Year
2007
Total Cost
$7,527
Indirect Cost
Name
Cleveland Clinic Lerner
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
135781701
City
Cleveland
State
OH
Country
United States
Zip Code
44195
Rose, Jonathan A; Wanner, Nicholas; Cheong, Hoi I et al. (2016) Flow Cytometric Quantification of Peripheral Blood Cell ?-Adrenergic Receptor Density and Urinary Endothelial Cell-Derived Microparticles in Pulmonary Arterial Hypertension. PLoS One 11:e0156940
Kasumov, Takhar; Solomon, Thomas P J; Hwang, Calvin et al. (2015) Improved insulin sensitivity after exercise training is linked to reduced plasma C14:0 ceramide in obesity and type 2 diabetes. Obesity (Silver Spring) 23:1414-21
Alkhouri, N; Eng, K; Cikach, F et al. (2015) Breathprints of childhood obesity: changes in volatile organic compounds in obese children compared with lean controls. Pediatr Obes 10:23-9
Rose, Jonathan A; Erzurum, Serpil; Asosingh, Kewal (2015) Biology and flow cytometry of proangiogenic hematopoietic progenitors cells. Cytometry A 87:5-19
Naples, Robert; Laskowski, Dan; McCarthy, Kevin et al. (2015) Carboxyhemoglobin and methemoglobin in asthma. Lung 193:183-7
Wu, Wei; Bleecker, Eugene; Moore, Wendy et al. (2014) Unsupervised phenotyping of Severe Asthma Research Program participants using expanded lung data. J Allergy Clin Immunol 133:1280-8
Li, Xingnan; Hawkins, Gregory A; Ampleford, Elizabeth J et al. (2013) Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients. J Allergy Clin Immunol 132:313-20.e15
Asosingh, Kewal; Farha, Samar; Lichtin, Alan et al. (2012) Pulmonary vascular disease in mice xenografted with human BM progenitors from patients with pulmonary arterial hypertension. Blood 120:1218-27
Yip, Kathleen; Heinberg, Leslie; Giegerich, Victoria et al. (2012) Equivalent weight loss with marked metabolic benefit observed in a matched cohort with and without type 2 diabetes 12 months following gastric bypass surgery. Obes Surg 22:1723-9
Li, Xingnan; Ampleford, Elizabeth J; Howard, Timothy D et al. (2012) Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases. J Allergy Clin Immunol 130:861-8.e7

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