2008
DOI: 10.1210/jc.2007-1825
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Rosiglitazone Reduces Liver Fat and Insulin Requirements and Improves Hepatic Insulin Sensitivity and Glycemic Control in Patients with Type 2 Diabetes Requiring High Insulin Doses

Abstract: Background: Liver fat is an important determinant of insulin requirements during insulin therapy. Peroxisome proliferator-activated receptor (PPAR)-␥ agonists reduce liver fat. We therefore hypothesized that type 2 diabetic patients using exceptionally high doses of insulin might respond well to addition of a PPAR␥ agonist.

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Cited by 50 publications
(38 citation statements)
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“…By contrast to metformin, TZDs improve whole-body insulin sensitivity during hyperinsulinemic-euglycemic clamp studies in patients with T2DM [93,94], reflecting an increase in peripheral glucose disposal. Although both metformin and TZDs decrease hepatic glucose production, only TZDs decrease liver fat content [93,95]. The partitioning of lipids to WAT (i.e., "lipid steal" hypothesis) following TZD treatment likely accounts for the indirect improvement in skeletal muscle insulin sensitivity and the reduction in liver steatosis, similar to what is seen in animal models.…”
Section: Insulin Sensitizers: Metformin and Thiazolidinedionesmentioning
confidence: 88%
“…By contrast to metformin, TZDs improve whole-body insulin sensitivity during hyperinsulinemic-euglycemic clamp studies in patients with T2DM [93,94], reflecting an increase in peripheral glucose disposal. Although both metformin and TZDs decrease hepatic glucose production, only TZDs decrease liver fat content [93,95]. The partitioning of lipids to WAT (i.e., "lipid steal" hypothesis) following TZD treatment likely accounts for the indirect improvement in skeletal muscle insulin sensitivity and the reduction in liver steatosis, similar to what is seen in animal models.…”
Section: Insulin Sensitizers: Metformin and Thiazolidinedionesmentioning
confidence: 88%
“…In diabetic patients, any type of treatment may modify the natural state of insulin action and/or secretion, unless the patient is studied at diagnosis before institution of any therapy or unless treatment is discontinued for prolonged periods, neither of which is ethically acceptable. However, the scientific literature, replete with such experiments that have the same limitations, has remarkably advanced our understanding of the pathophysiological changes in insulin action and secretion in T2DM and their modulations with various therapeutic approaches (36,37). Also, diabetics with an HbA1C above 8.5% were not studied, and it is possible that the strength of the correlations between surrogate indices may vary with the level of glycemic control.…”
Section: Discussionmentioning
confidence: 99%
“…gov Identifier: NCT00063635). Also, thiazolidinediones, such as pioglitazone and rosiglitazone, have been used successfully for improving insulin resistance and possibly liver histology in adults, but their use in children still requires an accurate control study before they can be considered for use in clinical practice [53][54][55] .…”
Section: Insulin Sensitizersmentioning
confidence: 99%