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胰岛素抵抗中的脂质代谢紊乱

[Disorders of lipid metabolism in insulin resistance].

作者信息

Müller-Wieland D, Krone W

机构信息

Klinik II und Poliklinik für Innere Medizin, Universität zu Köln.

出版信息

Herz. 1995 Feb;20(1):33-46.

PMID:7713475
Abstract

Insulin resistance with consecutive hyperinsulinemia is associated with dyslipidemia in individuals with metabolic syndrome or "syndrome x". This dyslipidemia is characterized by a hypertriglyceridemia and reduced levels of HDL-(high density lipoprotein)cholesterol in plasma. Table 1 summarizes the alterations of lipoproteins in insulin resistance. In severe forms of insulin resistance LDL-(low density lipoprotein)cholesterol can be elevated as well. The hypertriglyceridemia is caused by an elevated synthesis and secretion of VLDL (very low density lipoprotein) in the liver and by reduced metabolism, mediated e.g. by lipoprotein lipase. The alterations of VLDL-metabolism are associated with a reduced concentration of HDL-cholesterol. In addition the composition of lipoprotein particles can be altered, which might interfere with their normal metabolism. Furthermore addition direct effects of insulin on cellular cholesterol metabolism have been described. These alterations in lipid metabolism which are due to an insulin resistance and hyperinsulinemia might be related to the increased coronary risk which has been observed in patients with metabolic syndrome. Therefore the diagnostic approach in patients with hypertriglyceridemia should consider the possibility of an underlying glucose intolerance or Type 2 diabetes. Therapeutic aims and strategies are discussed. In accordance to guidelines of the American Heart Association the goals of lipid-lowering therapy take into account the prevalence of various cardiovascular risk factors in an individual patient (Table 2). Principle actions of lipid-lowering drugs on plasma lipids are outlined in Table 3. Table 4 summarizes the effect of antihypertensive drugs on plasma lipids and lipoproteins, which should be considered in the treatment of patients with dyslipidemia.

摘要

在患有代谢综合征或“X综合征”的个体中,胰岛素抵抗伴连续性高胰岛素血症与血脂异常相关。这种血脂异常的特征是血浆中甘油三酯水平升高和高密度脂蛋白胆固醇水平降低。表1总结了胰岛素抵抗时脂蛋白的变化。在严重的胰岛素抵抗形式中,低密度脂蛋白胆固醇也可能升高。高甘油三酯血症是由肝脏中极低密度脂蛋白(VLDL)的合成和分泌增加以及代谢降低(例如由脂蛋白脂肪酶介导)引起的。VLDL代谢的改变与高密度脂蛋白胆固醇浓度降低有关。此外,脂蛋白颗粒的组成可能会改变,这可能会干扰其正常代谢。此外,还描述了胰岛素对细胞胆固醇代谢的直接影响。这些由胰岛素抵抗和高胰岛素血症引起的脂质代谢改变可能与代谢综合征患者中观察到的冠心病风险增加有关。因此,高甘油三酯血症患者的诊断方法应考虑潜在的葡萄糖耐量异常或2型糖尿病的可能性。文中讨论了治疗目标和策略。根据美国心脏协会的指南,降脂治疗的目标考虑了个体患者中各种心血管危险因素的患病率(表2)。表3概述了降脂药物对血浆脂质的主要作用。表4总结了抗高血压药物对血浆脂质和脂蛋白的影响,在血脂异常患者的治疗中应予以考虑。

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