Rosiglitazone improves insulin resistance but does not improve exercise capacity in individuals with impaired glucose tolerance: A randomized clinical study

Author:

Abushamat Layla A12,Schauer Irene E234,Low Wang Cecilia C2,Mitchell Stacey35,Herlache Leah2,Bridenstine Mark6,Durbin Roy7,Snell-Bergeon Janet K89,Regensteiner Judith G24,Reusch Jane EB234

Affiliation:

1. Department of Medicine, Baylor College of Medicine, Houston, TX, USA

2. Department of Medicine, University of Colorado Anschutz Medical Campus School of Medicine, Aurora, CO, USA

3. Endocrine Section, Denver Veterans Affairs Medical Center, Denver, CO, USA

4. Ludeman Family Center for Women’s Health Research, Aurora, CO, USA

5. Denver Endocrinology, Diabetes and Thyroid Center, Englewood, CO, USA

6. Banner Health Clinic, Loveland, CO, USA

7. Arbor Family Medicine PC, Westminster, CO, USA

8. Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO, USA

9. University of Colorado Anschutz Medical Campus School of Public Health, Aurora, CO, USA

Abstract

Dysmetabolic states, such as type 2 diabetes (T2D), characterized by insulin resistance (IR), are associated with fatty liver, increased cardiovascular disease (CVD) risk, and decreased functional exercise capacity (FEC). Rosiglitazone (RO) improves exercise capacity and IR in T2D. However, the effects of RO on FEC and other markers of CVD risk in prediabetes are unknown. We hypothesized that insulin sensitization with RO would improve exercise capacity and markers of CVD risk in participants with impaired glucose tolerance (IGT). Exercise performance (peak oxygen consumption and oxygen uptake kinetics), IR (homeostasis model assessment of IR and quantitative insulin sensitivity check index), and surrogate cardiovascular endpoints (coronary artery calcium (CAC) volume and density and C-reactive protein (CRP)) were measured in participants with IGT after 12 and 18 months of RO or placebo (PL). RO did not significantly improve exercise capacity. Glycemic measures and IR were significantly lower in people on RO compared to PL at 18 months. CAC volume progression was not different between PL and RO groups. RO did not improve exercise capacity during an 18-month intervention despite improved IR and glycemia in people with IGT. Future studies should explore why effects on FEC with RO occur in T2D but not IGT. Understanding these questions may help in targeting therapeutic approaches in T2D and IGT.

Funder

U.S. Department of Veterans Affairs

Doris Duke Charitable Foundation

Ludeman Family Center for Women’s Health Research

American Diabetes Association

GlaxoSmithKline

Colorado Clinical and Translational Sciences Institute

National Institutes of Health

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

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