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首页> 外文期刊>American Journal of Case Reports >Ineffective Subtilisin/Kexin Type 9 (PCSK9) Inhibitors Monotherapy in Dyslipidemia with Low-Density Lipoprotein Cholesterol (LDL-C) Receptor Abnormalities: A Report of 2 Cases
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Ineffective Subtilisin/Kexin Type 9 (PCSK9) Inhibitors Monotherapy in Dyslipidemia with Low-Density Lipoprotein Cholesterol (LDL-C) Receptor Abnormalities: A Report of 2 Cases

机译:无效枯草杆菌蛋白酶/ kexin型9(PCSK9)抑制剂在低密度脂蛋白胆固醇(LDL-C)受体异常的血脂血症中的单疗法:2例报告

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Case series Patients: Male, 44-year-old ? Female, 71-year-old Final Diagnosis: Resistance to PCSK9I overcomed by adding statin Symptoms: Dyslipidemia Medication: — Clinical Procedure: — Specialty: Cardiology Objective: Unusual or unexpected effect of treatment Background: Real-life data on the efficacy of monotherapy with PCSK9 inhibitors are scarce. Most cohort studies have examined populations that are not severely dyslipidemic and are receiving combined therapy rather than monotherapy. Case Reports: From a series of 167 alirocumab prescriptions, we present a case of complete nonresponse and one of low response to monotherapy with proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors in 2 patients with heterozygous familial hypercholesterolemia and abnormalities of the low-density lipoprotein cholesterol (LDL-C) receptor. In these cases, PCSK9 inhibitors were ineffective when used alone to reduce the LDL-C level, but the addition of statin led to a dramatic improvement. Conclusions: As PCSK9 inhibitors become more commonly prescribed, more cases of nonresponse to PCSK9 inhibitors will be identified. Prospective studies are needed to investigate the efficacy of treatment with the monoclonal antibodies PCSK9 inhibitors in the context of LDL-C receptor abnormalities and to determine whether a genetic explanation exists for interindividual differences in response.
机译:案例系列患者:男,44岁?女性,71岁的最终诊断:抵抗PCSK9i克服了他汀类药物症状:渗透血症药物: - 临床程序: - 专业:心脏病学目标:治疗背景不寻常或意外效果:单疗法的实际数据PCSK9抑制剂稀缺。大多数队列研究检测了没有严重渗透性的人群,并且正在接受组合治疗而不是单一疗法。案例报告:从一系列167个Alirocumab处方,我们提出了一个完全非响应的情况,对2例杂合子家族高胆固醇血症和低的异常的患者中具有Proprotein转化酶枯草杆菌素/ kexin型9(PCSK9)抑制剂的单药治疗的案例。密度脂蛋白胆固醇(LDL-C)受体。在这些情况下,当单独使用以降低LDL-C水平时,PCSK9抑制剂无效,但是汀类药物的增加导致了剧烈改善。结论:由于PCSK9抑制剂变得更常见,因此将识别更多对PCSK9抑制剂的非响应情况。需要在LDL-C受体异常的背景下探讨用单克隆抗体PCSK9抑制剂治疗的疗效,并确定是否存在响应中的接触差异的遗传解释。

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