4.7 Article

Effects of Combined Exenatide and Pioglitazone Therapy on Hepatic Fat Content in Type 2 Diabetes

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OBESITY
卷 19, 期 12, 页码 2310-2315

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NATURE PUBLISHING GROUP
DOI: 10.1038/oby.2011.152

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  1. Amylin Pharmaceuticals
  2. Eli-Lilly
  3. Takeda Pharmaceuticals
  4. Amylin
  5. Merck
  6. Novartis
  7. Astra Zenica
  8. BMS
  9. Sanofi-Aventis

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We examined the effects of combined pioglitazone (peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonist) and exenatide (GLP-1 receptor agonist) therapy on hepatic fat content and plasma adiponectin levels in patients with type 2 diabetes (T2DM). Twenty-one T2DM patients (age = 52 +/- 3 years, BMI = 32.0 +/- 1.5, hemoglobin A(1c) (HbA(1c)) = 8.2 +/- 0.4%) on diet and/or metformin received additional treatment with either pioglitazone 45 mg/day for 12 months (n = 10) or combined therapy with pioglitazone (45 mg/day) and exenatide (10 mu g subcutaneously twice daily) for 12 months (n = 11). At baseline, hepatic fat content and plasma adiponectin levels were similar between the two treatment groups. Pioglitazone reduced fasting plasma glucose (FPG) (P < 0.05), fasting free fatty acid (FFA) (P < 0.05), and HbA(1c) (Delta = 1.0%, P < 0.01), while increasing plasma adiponectin concentration by 86% (P < 0.05). Hepatic fat (magnetic resonance spectroscopy (MRS)) was significantly reduced following pioglitazone treatment (11.0 +/- 3.1 to 6.5 +/- 1.9%, P < 0.05). Plasma triglyceride concentration decreased by 14% (P < 0.05) and body weight increased significantly (Delta = 3.7 kg). Combined pioglitazone and exenatide therapy was associated with a significantly greater increase in plasma adiponectin (Delta = 193%) and a significantly greater decrease in hepatic fat (12.1 +/- 1.7 to 4.7 +/- 1.3%) and plasma triglyceride (38%) vs. pioglitazone therapy despite the lack of a significant change in body weight (Delta = 0.2 kg). Hepatic injury biomarkers aspartate aminotransferase and alanine aminotransferase (ALT) were significantly decreased by both treatments; however, the reduction in ALT was significantly greater following combined pioglitazone and exenatide therapy. We conclude that combined in patients with T2DM, pioglitazone and exenatide therapy is associated with a greater reduction in hepatic fat content as compared to the addition of pioglitazone therapy (Delta = 61% vs. 41%, P < 0.05).

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