Laufs Ulrich, Liao James K
Vascular Medicine Research, Brigham & Women's Hospital, 65 Landsdowne Street, Cambridge, MA 02139, USA.
Curr Atheroscler Rep. 2003 Sep;5(5):372-8. doi: 10.1007/s11883-003-0008-z.
Convincing evidence from basic research and animal studies shows that HMG CoA reductase inhibitors or statins, exert cardiovascular protective effects beyond cholesterol-lowering. Because of the central role of LDL-C in mediating vascular pathology and the efficacy of statins for lowering LDL-C, the clinical importance of these additional non-lipid effects remains to be determined. Nevertheless, there is growing evidence from recent clinical trials, which suggests that some of the beneficial effects of statins may be unrelated to changes in LDL-C. Indeed, in animal studies, many of the cholesterol-independent or “pleiotropic” effects of statins are due predominantly to inhibition of isoprenoid, but not cholesterol synthesis. Thus, with the recent findings of the HPS and ASCOT-LLA, the potential cholesterol-independent effects of statins have shifted the treatment strategy from numerical lipid parameters to the global assessment of cardiovascular risks.
来自基础研究和动物研究的有力证据表明,HMG CoA还原酶抑制剂或他汀类药物除了降低胆固醇外,还具有心血管保护作用。由于低密度脂蛋白胆固醇(LDL-C)在介导血管病变中起核心作用,且他汀类药物降低LDL-C有效,这些额外的非脂质效应的临床重要性仍有待确定。然而,最近的临床试验有越来越多的证据表明,他汀类药物的一些有益作用可能与LDL-C的变化无关。事实上,在动物研究中,他汀类药物许多不依赖胆固醇或“多效性”的作用主要是由于抑制类异戊二烯合成,而非胆固醇合成。因此,随着心脏保护研究(HPS)和盎格鲁-斯堪的纳维亚心脏结局试验-降脂治疗协作组研究(ASCOT-LLA)的最新发现,他汀类药物潜在的不依赖胆固醇的效应已将治疗策略从数值脂质参数转变为心血管风险的整体评估。
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