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西格列汀联合吡格列酮治疗对 2 型糖尿病患者肝内脂肪含量的影响。

Effects of combined exenatide and pioglitazone therapy on hepatic fat content in type 2 diabetes.

机构信息

Diabetes and Endocrinology Division, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Obesity (Silver Spring). 2011 Dec;19(12):2310-5. doi: 10.1038/oby.2011.152. Epub 2011 Jun 9.

Abstract

We examined the effects of combined pioglitazone (peroxisome proliferator-activated receptor-γ (PPAR-γ) 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 µg 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) (Δ = 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 (Δ = 3.7 kg). Combined pioglitazone and exenatide therapy was associated with a significantly greater increase in plasma adiponectin (Δ = 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 (Δ = 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 (Δ = 61% vs. 41%, P < 0.05).

摘要

我们研究了吡格列酮(过氧化物酶体增殖物激活受体-γ(PPAR-γ)激动剂)和艾塞那肽(GLP-1 受体激动剂)联合治疗对 2 型糖尿病(T2DM)患者肝脂肪含量和血浆脂联素水平的影响。21 例 T2DM 患者(年龄=52±3 岁,BMI=32.0±1.5,糖化血红蛋白(HbA(1c))=8.2±0.4%)在饮食和/或二甲双胍的基础上加用吡格列酮 45mg/天治疗 12 个月(n=10)或联合吡格列酮(45mg/天)和艾塞那肽(10μg 皮下,每日 2 次)治疗 12 个月(n=11)。基线时,两组患者肝脂肪含量和血浆脂联素水平相似。吡格列酮降低空腹血糖(FPG)(P<0.05)、空腹游离脂肪酸(FFA)(P<0.05)和 HbA(1c)(Δ=1.0%,P<0.01),同时血浆脂联素浓度增加 86%(P<0.05)。吡格列酮治疗后肝脂肪(磁共振波谱(MRS))显著减少(11.0±3.1 至 6.5±1.9%,P<0.05)。血浆甘油三酯浓度降低 14%(P<0.05),体重显著增加(Δ=3.7kg)。与吡格列酮治疗相比,联合应用吡格列酮和艾塞那肽治疗可显著增加血浆脂联素(Δ=193%),显著降低肝脂肪(12.1±1.7 至 4.7±1.3%)和血浆甘油三酯(38%),尽管体重无显著变化(Δ=0.2kg)。两种治疗方法均显著降低天冬氨酸转氨酶和丙氨酸转氨酶等肝损伤生物标志物;然而,联合应用吡格列酮和艾塞那肽治疗后,丙氨酸转氨酶的降低更为显著。我们的结论是,与加用吡格列酮治疗相比,联合应用吡格列酮和艾塞那肽治疗 2 型糖尿病患者,肝脂肪含量的降低更为显著(Δ=61%对 41%,P<0.05)。

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