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J Clin Endocrinol Metab. 2001 Jan;86(1):280-8.

Rosiglitazone monotherapy is effective in patients with type 2 diabetes.

Author information

1
Department of Medicine, State University of New York, Brooklyn, New York 11203, USA. hlebovitz@attglobal.net

Erratum in

  • J Clin Endocrinol Metab 2001 Apr;86(4):1659.
  • J Clin Endocrinol Metab. 2002 Feb;2(1):iv..

Abstract

This study evaluated the efficacy and safety of rosiglitazone monotherapy in patients with type 2 diabetes. After a 4-week placebo run-in period, 493 patients with type 2 diabetes were randomized to receive rosiglitazone [2 or 4 mg twice daily (bd)] or placebo for 26 weeks. The primary end point was change in hemoglobin A(1c); other variables assessed included fasting plasma glucose, fructosamine, endogenous insulin secretion, urinary albumin excretion, serum lipids, and adverse events. Rosiglitazone (2 and 4 mg bd) decreased mean hemoglobin A(1c) relative to placebo by 1.2 and 1.5 percentage points, respectively, and reduced fasting plasma glucose concentrations relative to placebo by 3.22 and 4.22 mmol/L, respectively. Fasting plasma insulin and insulin precursor molecules decreased significantly. Homeostasis model assessment estimates indicate that rosiglitazone (2 and 4 mg bd) reduced insulin resistance by 16.0% and 24.6%, respectively, and improved ss-cell function over baseline by 49.5% and 60.0%, respectively. Urinary albumin excretion decreased significantly in the rosiglitazone (4 mg bd) group. There was no increase in adverse events with rosiglitazone. In the short-term, rosiglitazone is an insulin sensitizer that is effective and safe as monotherapy in patients with type 2 diabetes who are inadequately controlled by lifestyle interventions.

PMID:
11232013
DOI:
10.1210/jcem.86.1.7157
[Indexed for MEDLINE]

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