Rosiglitazone monotherapy improves glycaemic control in patients with type 2 diabetes: a twelve-week, randomized, placebo-controlled study
- PMID: 11220295
- DOI: 10.1046/j.1463-1326.1999.00020.x
Rosiglitazone monotherapy improves glycaemic control in patients with type 2 diabetes: a twelve-week, randomized, placebo-controlled study
Abstract
Aim: Rosiglitazone is the most potent of the thiazolidinediones, a novel class of oral antidiabetic agents that reduce blood glucose levels by sensitizing peripheral tissues to insulin. This study was designed to identify doses of rosiglitazone that would lower fasting plasma glucose (FPG) in patients with type 2 diabetes.
Methods: In this 12-week, double-blind, multicentre study, 380 patients with FPG values > or =7.8 mmol/L (140 mg/dL) and < or =13.3 mmol/L (240 mg/dL) were randomly assigned to receive treatment with placebo or rosiglitazone, 0.05, 0.25, 1.0, or 2.0 mg twice daily. The primary efficacy parameter was changed in FPG from baseline after 12 weeks of treatment. Secondary endpoints were changes in HbA1c, fructosamine, C peptide, insulin, lipid levels, and body weight (b.w.). Safety monitoring included clinical laboratory evaluations, electrocardiography, and echocardiography.
Results: Rosiglitazone 1.0 and 2.0 mg b.i.d. produced significant decreases in FPG (p=0.0001). Fructosamine also decreased in patients treated with these two dosages (p=0.003 in the 2.0 mg b.i.d. group). Rosiglitazone 2.0 mg b.i.d. significantly reduced plasma insulin levels (p=0.0044) and free fatty acids (p=0.0014) compared with placebo. Total cholesterol (p=0.0001), HDL (p=0.0009), and LDL (p=0.0001) increased in the rosiglitazone 2.0 mg b.i.d. group, but there was no significant change in the total cholesterol/HDL ratio or triglyceride levels in any rosiglitazone treatment group. Clinically insignificant dose-dependent increases in b.w. were observed in the rosiglitazone 1.0 and 2.0 mg b.i.d. treatment groups.
Conclusions: Twelve weeks of treatment with rosiglitazone 2.0 mg b.i.d. significantly decreases fasting plasma glucose, fructosamine, plasma insulin, and free fatty acids in patients with type 2 diabetes. Longer studies using higher doses will be needed to assess the efficacy and safety of rosiglitazone in patients with type 2 diabetes mellitus.
Similar articles
-
Addition of low-dose rosiglitazone to sulphonylurea therapy improves glycaemic control in Type 2 diabetic patients.Diabet Med. 2000 Jan;17(1):40-7. doi: 10.1046/j.1464-5491.2000.00224.x. Diabet Med. 2000. PMID: 10691158 Clinical Trial.
-
Once- and twice-daily dosing with rosiglitazone improves glycemic control in patients with type 2 diabetes.Diabetes Care. 2001 Feb;24(2):308-15. doi: 10.2337/diacare.24.2.308. Diabetes Care. 2001. PMID: 11213884 Clinical Trial.
-
Rosiglitazone short-term monotherapy lowers fasting and post-prandial glucose in patients with type II diabetes.Diabetologia. 2000 Mar;43(3):278-84. doi: 10.1007/s001250050045. Diabetologia. 2000. PMID: 10768088 Clinical Trial.
-
Multicenter retrospective assessment of thiazolidinedione monotherapy and combination therapy in patients with type 2 diabetes: comparative subgroup analyses of glycemic control and blood lipid levels.Clin Ther. 2003;25 Suppl B:B64-80. doi: 10.1016/s0149-2918(03)80243-6. Clin Ther. 2003. PMID: 14553867 Review.
-
[Rosiglitazone (BRL-49653)].Nihon Rinsho. 2000 Feb;58(2):401-4. Nihon Rinsho. 2000. PMID: 10707565 Review. Japanese.
Cited by
-
Thiazolidinediones in type 2 diabetes mellitus: current clinical evidence.Drugs. 2003;63(13):1373-405. doi: 10.2165/00003495-200363130-00004. Drugs. 2003. PMID: 12825962 Review.
-
Rational drug design and PPAR agonists.Curr Diab Rep. 2005 Oct;5(5):340-5. doi: 10.1007/s11892-005-0091-3. Curr Diab Rep. 2005. PMID: 16188168 Review.
-
The effects of human CYP2C8 genotype and fluvoxamine on the pharmacokinetics of rosiglitazone in healthy subjects.Br J Clin Pharmacol. 2006 Dec;62(6):682-9. doi: 10.1111/j.1365-2125.2006.02706.x. Epub 2006 Jul 12. Br J Clin Pharmacol. 2006. PMID: 16856883 Free PMC article.
-
Sex-Based Selectivity of PPARγ Regulation in Th1, Th2, and Th17 Differentiation.Int J Mol Sci. 2016 Aug 18;17(8):1347. doi: 10.3390/ijms17081347. Int J Mol Sci. 2016. PMID: 27548145 Free PMC article.
-
Hepatotoxicity with thiazolidinediones: is it a class effect?Drug Saf. 2001;24(12):873-88. doi: 10.2165/00002018-200124120-00002. Drug Saf. 2001. PMID: 11735645 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical