Metabolic effects of muraglitazar in type 2 diabetic subjects
Aim: To assess the effect of muraglitazar, a dual peroxisome proliferator‐activated receptor (PPAR)γ‐α agonist, versus placebo on metabolic parameters and body composition in subjects with type 2 diabetes mellitus (T2DM). Methods: Twenty‐seven T2DM subjects received oral glucose tolerance test (OGTT...
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Veröffentlicht in: | Diabetes, obesity & metabolism obesity & metabolism, 2011-10, Vol.13 (10), p.893-902 |
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Sprache: | eng |
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Zusammenfassung: | Aim: To assess the effect of muraglitazar, a dual peroxisome proliferator‐activated receptor (PPAR)γ‐α agonist, versus placebo on metabolic parameters and body composition in subjects with type 2 diabetes mellitus (T2DM).
Methods: Twenty‐seven T2DM subjects received oral glucose tolerance test (OGTT), euglycaemic insulin clamp with deuterated glucose, measurement of total body fat (DEXA), quantitation of muscle/liver (MRS) and abdominal subcutaneous and visceral (MRI) fat, and then were randomized to receive, in addition to diet, muraglitazar (MURA), 5 mg/day, or placebo (PLAC) for 4 months.
Results: HbA1cc decreased similarly (2.1%) during both MURA and PLAC treatments despite significant weight gain with MURA (+2.5 kg) and weight loss with PLAC (−0.7 kg). Plasma triglyceride, LDL cholesterol, free fatty acid (FFA), hsCRP levels all decreased with MURA while plasma adiponectin and HDL cholesterol increased (p < 0.05–0.001). Total body (muscle), hepatic and adipose tissue sensitivity to insulin and β cell function all improved with MURA (p < 0.05–0.01). Intramyocellular, hepatic and abdominal visceral fat content decreased, while total body and subcutaneous abdominal fat increased with MURA (p < 0.05–0.01).
Conclusions: Muraglitazar (i) improves glycaemic control by enhancing insulin sensitivity and β cell function in T2DM subjects, (ii) improves multiple cardiovascular risk factors, (iii) reduces muscle, visceral and hepatic fat content in T2DM subjects. Despite similar reduction in A1c with PLAC/diet, insulin sensitivity and β cell function did not improve significantly. |
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ISSN: | 1462-8902 1463-1326 |
DOI: | 10.1111/j.1463-1326.2011.01429.x |