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The Effects of Medications Used for the Management of Diabetes and Obesity on Postprandial Lipid Metabolism

机译:用于治疗糖尿病和肥胖症的药物对餐后脂质代谢的影响

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Postprandial lipemia has emerged as an independent risk factor for coronary artery disease. In this systematic review we examined the effect of the medications used for the management of diabetes, obesity and dyslipidemia on postprandial lipemia. It should be mentioned that no standardization exists for a test meal and for the duration of observation postprandially to allow for direct comparisons between the published studies. Type 2 diabetes mellitus and insulin resistance are associated with enhanced postprandial lipemia. Insulin is effective in reducing both fasting and post prandial total triglyceride levels as well as triglycerides contained in the triglyceride-rich lipoprotein sub-fractions. Additionally, the newer rapid-acting insulin analogues seem to be more effective in the reduction of postprandial lipemia than the short-acting human insulins. Acarbose ameliorates postprandial lipemia and reduces the atherogenic chylomicron and very low density lipoprotein remnants. Metformin reduces both fasting and postprandial triglyceridemia, fasting and postprandial free fatty acids and may increase the concentrations of the high density lipoprotein cholesterol. Sulfonylureas reduce fasting and postprandial triglyceride levels while data on the effect on high density lipoprotein levels are inconsistent. The effect of meglitinides on postprandial lipid metabolism is neutral. Rosiglitazone decreases fasting and postprandial free fatty acids but has no significant effect on fasting and postprandial triglycerides. Pioglitazone has additional beneficial effects on lipid metabolism because it reduces postprandial free fatty acids, fasting and postprandial triglycerides and increases high density lipoprotein cholesterol levels. Limited available data suggest that glucagon-like peptide- 1 analogues and vildagliptin reduce postprandial lipemia through reduction of intestinally-derived triglycerides. No data exist on the effect of sitagliptin on postprandial lipemia. Orlistat improves postprandial lipemia by reducing the absorption of the dietary fat; no data exist on the effect of sibutramine and rimonabant on the metabolism of lipids in the postprandial state.
机译:餐后血脂已成为冠状动脉疾病的独立危险因素。在这项系统评价中,我们检查了用于治疗糖尿病,肥胖和血脂异常的药物对餐后血脂的影响。应该提到的是,对于餐食和餐后观察的持续时间不存在标准化,以允许在已发表的研究之间进行直接比较。 2型糖尿病和胰岛素抵抗与餐后血脂升高有关。胰岛素可有效降低空腹和餐后总甘油三酯水平以及富含甘油三酸酯的脂蛋白亚组分中所含的甘油三酸酯。此外,较之速效人胰岛素,新型速效胰岛素类似物似乎在减少餐后血脂方面更有效。阿卡波糖改善餐后血脂,减少动脉粥样硬化性乳糜微粒和极低密度脂蛋白残留。二甲双胍可降低禁食和餐后甘油三酸酯血症,禁食和餐后游离脂肪酸,并可能增加高密度脂蛋白胆固醇的浓度。磺脲类药物可降低禁食和餐后甘油三酯水平,但有关高密度脂蛋白水平影响的数据不一致。美格替尼对餐后脂质代谢的影响是中性的。罗格列酮减少空腹和餐后游离脂肪酸,但对空腹和餐后甘油三酯无明显影响。吡格列酮对脂质代谢具有额外的有益作用,因为它可以减少餐后游离脂肪酸,禁食和餐后甘油三酸酯并增加高密度脂蛋白胆固醇水平。有限的可用数据表明,胰高血糖素样肽-1类似物和维格列汀可通过减少肠源性甘油三酸酯来降低餐后血脂。没有关于西他列汀对餐后血脂的影响的数据。奥利司他通过减少膳食脂肪的吸收来改善餐后血脂。尚无有关西布曲明和利莫那班对餐后状态下脂质代谢的影响的数据。

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