Eligibility for PCSK9 Inhibitors According to American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) Guidelines After Acute Coronary Syndromes

被引:35
|
作者
Gencer, Baris [1 ]
Koskinas, Konstantinos C. [2 ]
Raber, Lorenz [2 ]
Karagiannis, Alexios [3 ,4 ]
Nanchen, David [5 ]
Auer, Reto [6 ]
Carballo, David [1 ]
Carballo, Sebastian [1 ]
Klingenberg, Roland [7 ]
Heg, Dik [3 ,4 ]
Matter, Christian M. [7 ]
Luscher, Thomas F. [7 ]
Rodondi, Nicolas [6 ,8 ]
Mach, Francois [1 ]
Windecker, Stephan [2 ]
机构
[1] Geneva Univ Hosp, Div Cardiol, Geneva, Switzerland
[2] Univ Hosp Bern, Dept Cardiol, Bern, Switzerland
[3] Univ Bern, Clin Trials Unit Bern, Bern, Switzerland
[4] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
[5] Univ Lausanne, Dept Ambulatory Care & Community Med, Lausanne, Switzerland
[6] Univ Bern, Inst Primary Hlth Care BIHAM, Bern, Switzerland
[7] Univ Hosp Zurich, Univ Heart Ctr, Dept Cardiol, Zurich, Switzerland
[8] Univ Hosp Bern, Dept Gen Internal Med, Bern, Switzerland
来源
基金
瑞士国家科学基金会;
关键词
lipids; PCSK9; secondary prevention; FAMILIAL HYPERCHOLESTEROLEMIA; REDUCING LIPIDS; STATIN THERAPY; EFFICACY; SAFETY; IMPACT; CHOLESTEROL; RISK;
D O I
10.1161/JAHA.117.006537
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-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. Methods and Results-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 (P<0.001). Conclusions-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.
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页数:20
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