首页> 外文期刊>Journal of clinical lipidology >Achieved LDL cholesterol levels in patients with heterozygous familial hypercholesterolemia: A?model that explores the efficacy of conventional and novel lipid-lowering therapy
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Achieved LDL cholesterol levels in patients with heterozygous familial hypercholesterolemia: A?model that explores the efficacy of conventional and novel lipid-lowering therapy

机译:杂合子患者达到LDL胆固醇水平:a?模型探讨常规和新型降脂治疗的疗效

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BackgroundA large proportion of patients with heterozygous familial hypercholesterolemia (heFH) do not reach low-density lipoprotein cholesterol (LDL-c) levels advocated by international guidelines (<70?mg/dL or <100?mg/dL). ObjectiveWe set out to model which proportion of patients reach targets using conventional and novel therapies. MethodsWe performed a cross-sectional analysis in a large cohort of genetically identified heFH patients and calculated the proportion reaching treatment targets in four scenarios: (1) after 50% LDL-c reduction (representing maximal dose statin); (2) after 70% LDL-c reduction (maximal dose statin?+?ezetimibe); (3) additional 40% LDL-c reduction representing cholesteryl ester transfer protein inhibitor (CETPi); and (4) 60% LDL-c reduction (proprotein convertase subtilisin/kexin type 9 inhibitors [PCSK9i]), on top of scenario 2. We applied 100% adherence rates and literature-based adherence rates from 62% to 80%. ResultsWe included 1,059 heFH patients with and 9,420 heFH patients without coronary heart disease (CHD). With maximal dose statin, 8.3% and 48.1% of patients with and without CHD would reach their recommended LDL-c targets, respectively. This increases to 54.3% and 93.2% when ezetimibe is added. Addition of CETPi increases these numbers to 95.7% and 99.7%, whereas adding PCSK9i would result in 99.8% and 100% goal attainment. Using literature-based adherence rates, these numbers decrease to 3.8% and 27.3% for maximal dose statin, 5.8% and 38.9% combined with ezetimibe, 31.4% and 81.2% when adding CETPi, and 40.3% and 87.1% for addition of PCSK9i. ConclusionsLess than 10% with and 50% of heFH patients without CHD would reach treatment targets with maximal dose statin, but this substantially increases on addition of ezetimibe, CETPi, or PCSK9i. However, considering recently published adherence data, this might be lower in real life, especially in heFH patients with CHD.
机译:Backgrounta杂合族家族性高胆固醇血症(HEFH)的大部分不达到通过国际指南提倡的低密度脂蛋白胆固醇(LDL-C)水平(<70×mg / dl或<100×mg / dl)。目标掌握到使用常规和新疗法达到目标的模型。方法对遗传鉴定的HEFH患者的大群组进行了横截面分析,并计算了四种情况下的达到治疗靶标的比例:(1)减少50%(代表最大剂量他汀类药物)后; (2)70%LDL-C减少后(最大剂量他蛋白?+ ezetimibe); (3)额外的40%LDL-C还原代表胆甾醇酯转移蛋白抑制剂(CETPI); (4)60%LDL-C还原(Proprotein转化酶枯草杆菌素/ kexin型9抑制剂[PCSK9i]),在场景2.我们施加100%的粘附率和基于文学的粘附率,从62%到80%。 Resultswe包括1,059名Hefh患者,4,420名没有冠心病(CHD)。具有最大剂量调节蛋白,8.3%和48.1%的患者分别达到其推荐的LDL-C目标。添加ezetimibe时,这增加到54.3%和93.2%。加入CETPI增加这些数字至95.7%和99.7%,而添加PCSK9i将导致99.8%和100%的目标达到。利用基于文学的依从性率,最大剂量调节的数量减少至3.8%和27.3%,加入CETPI时的5.8%和38.9%,31​​.4%和81.2%,加入PCSK9i的40.3%和87.1%。结论不超过10%,50%的HEFH患者没有CHD将达到具有最大剂量调节蛋白的治疗靶标,但由于添加ezetimibe,CETPI或PCSK9i,这显着增加。然而,考虑到最近公布的依从性数据,这可能在现实生活中较低,特别是在HEFH患有CHD患者中。

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