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Management of Hypercholesterolemia Appropriateness of Therapeutic Approaches and New Drugs in Patients with High Cardiovascular Risk

机译:高胆固醇风险患者的高胆固醇血症治疗方法和新药的适当性管理

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摘要

Control of lipid levels is one of the most effective strategies for cardiovascular (CV) event prevention. In fact, many clinical trials have clearly demonstrated that low-density lipoprotein cholesterol (LDL-C) lowering, primarily with statins, reduces major CV events and mortality. The evidence from these trials has been useful in designing the cholesterol treatment guidelines, which are mainly aimed at preventing and managing cardiovascular disease (CVD). However, available data indicate that a large proportion of patients fail to achieve lipid goals, and this is particularly frequent in patients at high or very high CV risk. Furthermore, owing to side effects, a significant percentage of patients cannot tolerate statin treatment. Hence, researchers have focused their attention on novel LDL-C-lowering agents that act via mechanisms distinct from that of statins. Among the new compounds under investigation, the monoclonal antibodies to proprotein convertase subtilisin/kexin type 9 (PCSK9) seem particularly promising, having recently been shown to be well tolerated and highly effective at lowering LDL-C, with a possible effect on the occurrence of CV events. Currently, alirocumab is approved by the US Food and Drug Administration (FDA) as an adjunct to diet and maximally tolerated statin therapy for use in adults with heterozygous familial hypercholesterolemia (FH) or those with atherosclerotic CV disease who require additional LDL-C lowering; it has also been recently approved by the European Medicines Agency (EMA) for use in patients with heterozygous FH, non–familial hypercholesterolemia or mixed dyslipidemia in whom statins are ineffective or not tolerated. Evolocumab is approved by the FDA as an adjunct to diet and maximally tolerated statins for adults with hetero- and homozygous FH and those with atherosclerotic CV disease who require additional lowering of LDL-C, and by the EMA in adults with primary hypercholesterolemia or mixed dyslipidemia, as an adjunct to diet, in combination with a statin or a statin with other lipid lowering therapies in patients unable to reach LDL-C goals with the maximum tolerated dose of a statin; alone or in combination with other lipid lowering therapies in patients who are statin-intolerant, or those for whom a statin is contraindicated. Evolocumab is also indicated in adults and adolescents aged 12 years and over with homozygous familial hypercholesterolemia in combination with other lipid-lowering therapies.
机译:控制脂质水平是预防心血管(CV)事件的最有效策略之一。实际上,许多临床试验已经清楚地表明,主要通过他汀类药物降低低密度脂蛋白胆固醇(LDL-C)可以降低主要的心血管事件和死亡率。这些试验的证据可用于设计胆固醇治疗指南,该指南主要针对预防和管理心血管疾病(CVD)。但是,现有数据表明,很大一部分患者未能达到血脂目标,在高或非常高的CV风险患者中尤为常见。此外,由于副作用,很大一部分患者不能耐受他汀类药物的治疗。因此,研究人员将注意力集中在通过与他汀类药物不同的机制起作用的新型降低LDL-C的药物上。在正在研究的新化合物中,针对前蛋白转化酶枯草杆菌蛋白酶/ kexin 9型的单克隆抗体(PCSK9)似乎特别有前途,最近已被证明具有良好的耐受性,并且在降低LDL-C方面非常有效,并可能对降低LDL-C产生影响。简历事件。目前,alirocumab已被美国食品和药物管理局(FDA)批准作为饮食和最大耐受他汀类药物的辅助药物,用于患有杂合性家族性高胆固醇血症(FH)或需要进一步降低LDL-C的动脉粥样硬化性CV疾病的成年人;最近,它还被欧洲药品管理局(EMA)批准用于他汀类药物无效或不能耐受的杂合性FH,非家族性高胆固醇血症或混合血脂异常的患者。 Evolocumab已被FDA批准为杂合子和纯合子FH成年人和需要进一步降低LDL-C的动脉粥样硬化性CV病患者的饮食和最大耐受他汀类药物的辅助药物,并已通过EMA批准用于原发性高胆固醇血症或混合血脂异常的成年人作为饮食的辅助手段,在他汀类药物的最大耐受剂量无法达到LDL-C目标的患者中,应与他汀类药物或他汀类药物联合其他降脂治疗结合使用;在不接受他汀类药物治疗或禁忌他汀类药物的患者中单独或与其他降脂疗法联合使用。 Evolocumab还适用于12岁及以上的成年人和纯合子家族性高胆固醇血症并结合其他降脂治疗的青少年。

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