Effects of Rosiglitazone, Glyburide, and Metformin on β-Cell Function and Insulin Sensitivity in ADOPT

Author:

Kahn Steven E.1,Lachin John M.2,Zinman Bernard3,Haffner Steven M.4,Aftring R. Paul5,Paul Gitanjali5,Kravitz Barbara G.5,Herman William H.6,Viberti Giancarlo7,Holman Rury R.8,

Affiliation:

1. Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, VA Puget Sound Health Care System and University of Washington, Seattle, Washington

2. Biostatistics Center, George Washington University, Rockville, Maryland

3. Samuel Lunenfeld Research Institute, Mount Sinai Hospital and University of Toronto, Ontario, Canada

4. San Antonio Texas

5. GlaxoSmithKline, King of Prussia, Pennsylvania

6. Departments of Internal Medicine and Epidemiology, University of Michigan, Ann Arbor, Michigan

7. King’s College London School of Medicine, King’s College London, London, U.K.

8. Diabetes Trials Unit, Oxford Centre for Diabetes, Endocrinology and Metabolism, Oxford University, Oxford, U.K.

Abstract

OBJECTIVE ADOPT (A Diabetes Outcome Progression Trial) demonstrated that initial monotherapy with rosiglitazone provided superior durability of glycemic control compared with metformin and glyburide in patients with recently diagnosed type 2 diabetes. Herein, we examine measures of β-cell function and insulin sensitivity from an oral glucose tolerance test (OGTT) over a 4-year period among the three treatments. RESEARCH DESIGN AND METHODS Recently diagnosed, drug-naïve patients with type 2 diabetes (4,360 total) were treated for a median of 4.0 years with rosiglitazone, metformin, or glyburide and were examined with periodic metabolic testing using an OGTT. RESULTS Measures of β-cell function and insulin sensitivity from an OGTT showed more favorable changes over time with rosiglitazone versus metformin or glyburide. Persistent improvements were seen in those who completed 4 years of monotherapy and marked deterioration of β-cell function in those who failed to maintain adequate glucose control with initial monotherapy. CONCLUSIONS The favorable combined changes in β-cell function and insulin sensitivity over time with rosiglitazone appear to be responsible for its superior glycemic durability over metformin and glyburide as initial monotherapy in type 2 diabetes.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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