HMG-CoA还原酶抑制剂治疗高脂血症

R Prager
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引用次数: 0

摘要

hmg -辅酶a还原酶抑制剂是一类有趣的新型降胆固醇物质。目前,这些物质中只有一种在奥地利注册,即洛伐他汀(Mevacor)。hmg -辅酶a还原酶抑制剂主要通过增加ldl受体的表达而起作用,可能是在肝脏中。通过这种机制,它们可以显著降低低密度脂蛋白胆固醇水平,从而显著降低患冠心病的风险。这些药物每日一次的剂量、低剂量的有效性和低副作用的发生率有利于患者的依从性。除了在避免与贝特酸类似物或环孢素联合治疗时很少发生的横纹肌溶解外,这种治疗相对没有严重的副作用。长期研究结果表明,这些药物的降胆固醇作用在长期治疗期间保持不变;可能的药物相关副作用与短期研究报告没有差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Treatment of hyperlipidemia with HMG-CoA reductase inhibitors].

HMG-CoA-reductase inhibitors represent an interesting new class of cholesterol-lowering substances. At the moment there is only one of these substances, lovastatin (Mevacor), registered in Austria. HMG-CoA-reductase inhibitors act primarily through an increase of the expression of the LDL-receptors presumably in the liver. By this mechanism they cause a marked reduction of LDL-cholesterol-levels and thus should markedly reduce the risk of coronary heart disease. The once daily dosage of these drugs, their effectiveness in low doses and the low incidence of side effects facilitate the patient's compliance. With the exception of rhabdomyolysis which occurs very rarely when avoiding a combination therapy with fibrate-analoges or cyclosporin, this kind of treatment is relatively free of serious side effects. Results from long-term studies indicate that the hypocholesterolemic effect of these drugs is maintained during prolonged therapy; possible drug-related side effects did not differ from those reported in short-term studies.

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