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The Obese Patient with Diabetes Mellitus: From Research Targets to Treatment Options

机译:肥胖的糖尿病患者:从研究目标到治疗选择

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Abdominal obesity is a recognized risk factor for both type 2 diabetes mellitus and cardiovascular disease. The metabolic consequences of obesity, such as insulin resistance and impaired glucose tolerance, are primarily attributable to visceral, rather than to subcutaneous, adipose tissue. As a result, liposuction, which mainly removes subcutaneous fat, has no significant effect on insulin sensitivity; by contrast, weight loss resulting from bariatric surgical procedures is associated with resolution of type 2 diabetes in almost 80% of patients. Even modest weight loss in overweight or obese individuals is associated with significant reductions in the risk of diabetes and increased survival. Recent studies have suggested that the renin-angiotensin system (RAS) functions in the regulation of adipogenesis. Activation of this system is increased in obese individuals and angiotensin II, acting via angiotensin type 1 receptors, inhibits the differentiation of preadipocytes into mature adipocytes. This mightbe expected to result in ectopic storage of fat in tissues such as skeletal muscle and liver, thereby decreasing insulin sensitivity. Evidence from animal studies suggests that angiotensin-receptor blockers can promote redistribution of excess fat from these ectopic sites to mature adipocytes, resulting in improved insulin sensitivity. Clinical trials with telmisartan are currently investigating the effects of RAS blockade on insulin sensitivity in humans
机译:腹部肥胖是2型糖尿病和心血管疾病的公认危险因素。肥胖的代谢后果,例如胰岛素抵抗和葡萄糖耐量降低,主要归因于内脏而非皮下脂肪组织。结果,主要去除皮下脂肪的抽脂对胰岛素敏感性没有显着影响。相反,减肥手术导致的体重减轻与将近80%的2型糖尿病消退有关。在超重或肥胖的人中,即使适度的体重减轻也与糖尿病风险的显着降低和存活率的提高有关。最近的研究表明,肾素-血管紧张素系统(RAS)在调节脂肪形成中起作用。在肥胖个体中该系统的激活增加,并且通过1型血管紧张素受体起作用的血管紧张素II抑制前脂肪细胞向成熟脂肪细胞的分化。可以预期这会导致脂肪异位储存在骨骼肌和肝脏等组织中,从而降低胰岛素敏感性。动物研究的证据表明,血管紧张素受体阻滞剂可促进多余脂肪从这些异位部位重新分布到成熟的脂肪细胞,从而改善胰岛素敏感性。替米沙坦的临床试验目前正在研究RAS阻断剂对人体胰岛素敏感性的影响

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