Journal Article

Rosiglitazone in the treatment of type 2 diabetes mellitus: a critical review

Malinowski, Jennifer M., Bolesta, Scott

2000

Overview

Objective: This article reviews the pharmacology, pharmacokinetics, clinical efficacy, adverse effects, drug interactions, and dosing of rosiglitazone, the second thiazolidinedione approved for the treatment of type 2 diabetes mellitus. Methods: Background information for this article was obtained from searches of MEDLINE®, Iowa Drug Information Service, and International Pharmaceutical Abstracts, as well as from data on file with the manufacturer of rosiglitazone. Results: Rosiglitazone is indicated for use alone or in combination with metformin or sulfonylureas for the maintenance of glycemic control in patients with type 2 diabetes mellitus. Rather than stimulation of insulin secretion, rosiglitazone's primary mechanism of action is sensitization of tissues to insulin through activation of the peroxisome proliferator-activated receptor gamma and increasing expression of the glucose transporter-4 receptor. Rosiglitazone is administered orally, is absorbed almost completely, and is 99.8% bound to plasma proteins. The majority of a dose is metabolized by the cytochrome P-450 2C8 isozyme, with the inactive metabolites excreted primarily in the urine. Four to 8 mg/d of rosiglitazone given alone or in combination with metformin, sulfonylureas, or insulin has produced reductions in baseline fasting plasma glucose and glycosylated hemoglobin in studies of up to 1 year's duration. Common adverse effects (occurring in ≥5.0% of patients) include upper respiratory tract infection, injury, and headache. Edema, weight gain, and increased low-density lipoprotein cholesterol concentrations have also been observed. It is recommended that rosiglitazone be avoided in patients with alanine aminotransferase levels > 2.5 times normal. No clinically relevant drug interactions have been documented with rosiglitazone to date. The initial starting daily dose of rosiglitazone is 4 mg in single or divided doses, without regard to meals, to a maximum of 8 mg. Conclusions: No direct comparative trials of the efficacy and safety of rosiglitazone versus those of the other available thiazolidinedione, pioglitazone, have yet been performed. The role of rosiglitazone as a single agent and in combination with other antidiabetic agents remains to be clarified as additional comparative and long-term data become available.

• Publisher: EM Inc USA,Excerpta Medica
• Subject: Aged / Area Under Curve / Biological and medical sciences / Biological Availability / Clinical Trials as Topic / Diabetes Mellitus, Type 2 - drug therapy / Drug Interactions / Drug Therapy, Combination / glycemic control / Hormones. Endocrine system / Humans / Hypoglycemic Agents - adverse effects / Hypoglycemic Agents - blood / Hypoglycemic Agents - pharmacokinetics / Hypoglycemic Agents - therapeutic use / Insulin - therapeutic use / Medical sciences / Metformin - therapeutic use / Middle Aged / Pharmacology. Drug treatments / rosiglitazone / Thiazoles - adverse effects / Thiazoles - blood / Thiazoles - pharmacokinetics / Thiazoles - therapeutic use / Thiazolidinediones / type 2 diabetes mellitus