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A review of newer treatment approaches for type-2 diabetes: Focusing safety and efficacy of incretin based therapy

机译:2型糖尿病的新治疗方法综述:以肠降血糖素为基础的治疗的重点安全性和有效性

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Diabetes resulting from both genetic and lifestyle factors causes high insulin deficiency or its resistance. As hyperglycemia and decreased insulin secretion and/or its sensitivity appear to be the primary defects associated with diabetes, available treatments focus on reducing those defects. A novel approach of treatment is to target the incretin mimetic hormones, which are secreted by intestinal cells in response to food intake, provoking glucose-dependent insulin secretion from the pancreas. Efficacy and safety studies of dipetidyl peptidase inhibitors (DPP-IV), sitagliptin, vildagliptin and linagliptin provide similar improvements in HbA1c levels when compared with metformin, sulfonylureas or glitazones without contributing to weight gain and hypoglycemia. Caution is required when choosing the gliptin in people with renal or hepatic impairment and with a risk of pancreatitis. The glucagon like peptide (GLP-1) analogues Exenatide and Liraglutide also have positive impact on glycemic control especially when used as a combination therapy. Another upcoming approach is using sodium-glucose co transporter two inhibitors in kidney, by exploring pathophysiology of renal glucose re absorption in the proximal tubule.
机译:由遗传因素和生活方式因素导致的糖尿病会导致高胰岛素缺乏或其抵抗力。由于高血糖和胰岛素分泌减少和/或其敏感性降低似乎是与糖尿病相关的主要缺陷,因此可用的治疗方法集中于减少这些缺陷。一种新的治疗方法是针对肠降血糖素模拟激素,该激素由肠道细胞响应食物摄入而分泌,促使胰腺分泌葡萄糖依赖性胰岛素。与二甲双胍,磺酰脲类或格列酮类相比,双哌啶基肽酶抑制剂(DPP-IV),西他列汀,维达列汀和利拉列汀的功效和安全性研究在HbA1c水平方面具有类似的改善,而不会增加体重和降低血糖。在肾或肝功能不全且有胰腺炎风险的人中选择胰蛋白酶时必须谨慎。胰高血糖素样肽(GLP-1)类似物艾塞那肽和利拉鲁肽也对血糖控制有积极影响,尤其是在用作联合疗法时。另一种即将到来的方法是通过探索近端肾小管中肾脏葡萄糖再吸收的病理生理,在肾脏中使用钠-葡萄糖共转运蛋白两种抑制剂。

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