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Effects of Exenatide on Diabetes, Obesity, Cardiovascular Risk Factors, and Hepatic Biomarkers in Patients with Type 2 Diabetes

机译:艾塞那肽对2型糖尿病患者糖尿病,肥胖,心血管危险因素和肝生物标志物的影响

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摘要

Obesity increases the risk of diabetes up to 90-fold and worsens hyperglycemia, hyperinsulinemia, insulin resistance, dyslipidemia, and nonalcoholic fatty liver disease. For patients with type 2 diabetes, weight loss can trigger improvements in all these conditions and decrease the need for glucose-lowering agents. The incretin mimetic exenatide shares many glucoregulatory properties with native glucagon-like peptide-1, including enhancement of glucose-dependent insulin secretion, glucose-dependent suppression of inappropriately high glucagon secretion, slowing of gastric emptying, and reduction of food intake in patients with type 2 diabetes. Exenatide treatment was associated with progressive weight loss in the majority of patients in clinical trials. In addition, patients with elevated markers of liver injury at baseline showed improvements. Therefore, exenatide represents a unique option for adjunctive therapy for patients with type 2 diabetes not achieving adequate glycemic control on oral antidiabetic agents, especially in patients for whom weight gain would be an additional contraindication.
机译:肥胖使糖尿病风险增加多达90倍,并使高血糖,高胰岛素血症,胰岛素抵抗,血脂异常和非酒精性脂肪肝恶化。对于2型糖尿病患者,减肥可以触发所有这些疾病的改善,并减少对降糖药的需求。肠降血糖素模拟艾塞那肽与天然胰高血糖素样肽1具有许多糖调节特性,包括增强葡萄糖依赖性胰岛素分泌,抑制葡萄糖依赖性地抑制不适当的高胰高血糖素分泌,减慢胃排空以及减少2型糖尿病患者的食物摄入量。 2糖尿病。在大多数临床试验中,艾塞那肽治疗与体重减轻有关。此外,基线时肝损伤指标升高的患者表现出改善。因此,艾塞那肽是2型糖尿病患者无法通过口服降糖药实现足够的血糖控制的辅助疗法的独特选择,尤其是对于体重增加将是另一禁忌症的患者。

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