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首页> 外文期刊>Hormones: International Journal of Endocrinology and Metabolism >Expert consensus on the rational clinical use of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors
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Expert consensus on the rational clinical use of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors

机译:关于前蛋白转化酶枯草杆菌蛋白酶/ kexin 9型(PCSK9)抑制剂的合理临床使用的专家共识

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摘要

Two proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, evolocumab and alirocumab, have recently been approved by both the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of hypercholesterolemia. These fully human monoclonal antibodies selectively block PCSK9, thus permitting the low-density lipoprotein (LDL) receptor to effectively recycle to the surface of liver cells. The administration of these antibodies leads to robust LDL cholesterol (LDL-C) lowering by 50-60% on top of maximum hypolipidemic treatment. At least 4 randomized, placebo-controlled studies are under way and will address the question of whether the administration of these PCSK9 inhibitors is associated with a significant reduction of cardiovascular events. Because of the high cost associated with the use of these medications it is very important to consider which patients may gain the most benefit, at least until the results of outcome studies are available. In this Consensus paper, 34 clinicians/scientists define 3 groups of patients that should be currently considered as candidates for the use of these novel drugs. These include: 1a. Adults with established cardiovascular disease and LDL-C≥100 mg/dL while on lifestyle modifications and maximally tolerated hypolipidemic treatment, i.e. high-intensity statin + ezetimibe, 1b. Adults with diabetes and established cardiovascular disease or chronic kidney disease or target organ damage and LDL-C ≥100 mg/dL while on lifestyle modifications and maximally tolerated hypolipidemic treatment, i.e. high-intensity statin + ezetimibe, 2. Adults with familial hypercholesterolemia (FH) without established cardiovascular disease and LDL-C ≥130 mg/dL while on lifestyle modifications and maximally tolerated hypolipidemic treatment, i.e. high-intensity statin + ezetimibe (evolocumab is also indicated in children above 12 years with homozygous FH), and 3. Adults at high or very high cardiovascular risk who are statin intolerant and have an LDL-C ≥100 and ≥130 mg/dL, respectively, while on any tolerated hypolipidemic treatment.
机译:两种前蛋白转化酶枯草杆菌蛋白酶/ kexin 9型(PCSK9)抑制剂evolocumab和alirocumab最近已获得美国食品药品管理局(FDA)和欧洲药品管理局(EMA)的批准,可用于治疗高胆固醇血症。这些完全人源的单克隆抗体选择性地阻断PCSK9,从而使低密度脂蛋白(LDL)受体有效地循环到肝细胞表面。这些抗体的施用导致最大的降血脂治疗之外,健壮的LDL胆固醇(LDL-C)降低了50-60%。正在进行至少4项随机,安慰剂对照的研究,这些研究将探讨这些PCSK9抑制剂的给药是否与心血管事件的显着减少有关的问题。由于使用这些药物的成本高昂,因此至少在获得结果研究结果之前,考虑哪些患者可能会受益最大是非常重要的。在这份共识文件中,有34位临床医生/科学家定义了3组患者,这些患者目前应被视为使用这些新药的候选人。其中包括:1a。患有确诊的心血管疾病且LDL-C≥100 mg / dL的成年人,同时进行生活方式改变和最大耐受的降血脂治疗,即高强度他汀+依泽替米贝1b。患有糖尿病和已确定的心血管疾病或慢性肾脏疾病或目标器官损害且LDL-C≥100 mg / dL的成年人,同时进行生活方式改变和最大耐受的降血脂治疗,即高强度他汀+依泽替米贝2。患有家族性高胆固醇血症(FH)的成年人),没有生活方式的改变,并且最大程度地接受了降血脂治疗,即高强度他汀+依泽替米贝(在12岁以上纯合子FH的儿童中也应使用evolocumab),且未接受过心血管疾病且LDL-C≥130mg / dL,且3岁。成人在任何耐受的降血脂治疗中,他汀类药物不耐受且LDL-C≥100和≥130mg / dL的心血管风险高或非常高的患者。

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