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Results of the Heart Protection Study: can we still assume a class effect?

机译:心脏保护研究结果:我们仍然可以假设课堂效果吗?

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Statins share several common features including the mechanism of action, i.e. inhibition of HMG-CoA reductase, as well as LDL-cholesterol (LDL-C) and triglyceride lowering properties. However, statins show minor differences in chemical structure, lipophilicity that could translate into a different pharmacological properties. For example, simvastatin exerted a more favorable effect on HDL-C levels than did atorvastatin when higher doses of the two drugs were compared.Finally, the major considerations to chose between statins for CVD patient therapy include clinical benefits and safety (i.e. evidence-based medicine). Primary prevention trials with pravastatins and Iovastatin and secondary prevention trials with pravastatin, fluvastatin and simvastatin have established the clinical benefits of statins. In addition, HPS study was designed to investigate the benefits of simvastatin 40 mg in a broad range of patients at high risk for heart disease including women, Hie elderly and those with a history of hearth attacks, diabetes, hypertension or vascular disease. The results show the ability of simvastatin to reduce all causes of mortality, vascular death and cardiovascular morbidity. The trial also confirms the safety of simvastatin 40 mg although 60% of patients were receiving additional pharmacological treatment. In summary, it appears that statins are not the same and the choice of the more appropriate statin in high-risk patients should be driven by the evidence-based medicine both in terms of safety and efficacy.
机译:他汀汀共享几种常见特征,包括作用机制,即HMG-CoA还原酶以及LDL-胆固醇(LDL-C)和甘油三酯降低性质。然而,他汀类药物显示出化学结构的微小差异,可转化为不同的药理学性质的亲脂性。例如,辛伐他汀对HDL-C水平的影响比Atorvastatin的比较更高,当较高剂量的比较时。最后,CVD患者治疗他汀类药物中选择的主要考虑因素包括临床效益和安全性(即证据药物)。用普伐他汀和普伐他汀,氟伐他汀和辛伐他汀和二级预防试验的主要预防试验已经确定了他汀类药物的临床益处。此外,HPS研究旨在探讨辛伐他汀40毫克在广泛风险的广泛患者中的益处,包括妇女,赫耶老人,患有壁炉攻击,糖尿病,高血压或血管疾病的人的高风险。结果表明辛伐他汀减少死亡,血管死亡和心血管发病率所有原因的能力。该试验还证实了辛伐他汀40毫克的安全性,尽管60%的患者接受了额外的药理学治疗。总之,似乎他汀类药物不一样,并且在安全性和疗效方面,应由循证医学引发更合适的他汀类药物的选择。

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