Division of Cardiology, Geneva University Hospital, Geneva, Switzerland
Department of Cardiology, University Hospital Bern, Switzerland.
J Am Heart Assoc. 2017 Nov 9;6(11):e006537. doi: 10.1161/JAHA.117.006537.
The American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) have recently published recommendations for the use of proprotein convertase subtilisin/kexin-9 (PCSK9) inhibitors in situations of very high risk. We aim to assess in the real world the suitability of PCSK9 inhibitors for acute coronary syndromes.
We analyzed a prospective Swiss cohort of 2023 patients hospitalized for acute coronary syndromes between 2009 and 2014 with available data for low-density lipoprotein cholesterol and lipid-lowering therapy at 1 year. Clinical familial hypercholesterolemia was defined using the Dutch Lipid Clinic Network algorithm as unlikely, possible, probable, or definite. We simulated a fixed relative reduction of 24% in low-density lipoprotein cholesterol levels at 1 year in all patients not treated with ezetimibe, irrespective of the low-density lipoprotein cholesterol levels and statin regimen. At 1 year, 94.3% of patients were treated with statin, 5.8% with ezetimibe, and 35.8% of patients had on-target low-density lipoprotein cholesterol levels (<1.8 mmol/L); 25.6% met criteria for possible or probable/definite familial hypercholesterolemia. After a simulation of the lipid-lowering effect of ezetimibe, the proportion of patients who would be eligible for PCSK9 inhibitors at 1 year was 13.4% using American College of Cardiology criteria and 2.7% using European Society of Cardiology/European Atherosclerosis Society criteria. Patients with possible or probable/definite familial hypercholesterolemia were more eligible for PCSK9 inhibitors compared with their non-familial hypercholesterolemia counterparts: 27.6% versus 8.8% according to American College of Cardiology criteria and 6.6% versus 1.8% according to European Society of Cardiology/European Atherosclerosis Society criteria (<0.001).
Recommendations made by the American College of Cardiology guidelines would lead to 5-fold higher eligibility rates for PCSK9 inhibitors compared to the European Society of Cardiology/European Atherosclerosis Society consensus statement in acute coronary syndrome patients.
美国心脏病学会(ACC)和欧洲心脏病学会/欧洲动脉粥样硬化学会(ESC/EAS)最近发布了关于在极高危情况下使用前蛋白转化酶枯草溶菌素/κexin-9(PCSK9)抑制剂的建议。我们旨在评估 PCSK9 抑制剂在急性冠状动脉综合征中的实际适用性。
我们分析了一项前瞻性瑞士队列研究,纳入了 2009 年至 2014 年期间因急性冠状动脉综合征住院的 2023 例患者,这些患者在 1 年内有低密度脂蛋白胆固醇和降脂治疗的数据。临床家族性高胆固醇血症采用荷兰脂质诊所网络算法定义为不太可能、可能、很可能或明确。我们模拟了所有未接受依折麦布治疗的患者在 1 年内低密度脂蛋白胆固醇水平降低 24%的固定相对降低,无论低密度脂蛋白胆固醇水平和他汀类药物治疗方案如何。在 1 年内,94.3%的患者接受了他汀类药物治疗,5.8%的患者接受了依折麦布治疗,35.8%的患者达到了目标低密度脂蛋白胆固醇水平(<1.8mmol/L);25.6%符合可能或很可能/明确的家族性高胆固醇血症标准。在用依折麦布模拟降脂作用后,根据美国心脏病学会标准,有 13.4%的患者在 1 年内有资格使用 PCSK9 抑制剂,而根据欧洲心脏病学会/欧洲动脉粥样硬化学会标准,有 2.7%的患者有资格使用 PCSK9 抑制剂。与非家族性高胆固醇血症患者相比,可能或很可能/明确的家族性高胆固醇血症患者更符合 PCSK9 抑制剂的使用条件:根据美国心脏病学会标准,有 27.6%的患者符合条件,而根据欧洲心脏病学会/欧洲动脉粥样硬化学会标准,有 6.6%的患者符合条件(<0.001)。
与欧洲心脏病学会/欧洲动脉粥样硬化学会共识声明相比,美国心脏病学会指南中的建议将使急性冠状动脉综合征患者使用 PCSK9 抑制剂的资格标准提高 5 倍。