LDL cholesterol target achievement in heterozygous familial hypercholesterolemia patients according to 2019 ESC/EAS lipid guidelines: Implications for newer lipid-lowering treatments

被引:23
作者
Rizos, Christos V. [1 ]
Skoumas, Ioannis [2 ]
Rallidis, Loukianos [3 ]
Skalidis, Emmanouil [4 ]
Tziomalos, Konstantinos [5 ]
Garoufi, Anastasia [6 ]
Anagnostis, Panagiotis [7 ]
Sfikas, George [8 ]
Kotsis, Vasileios [9 ]
Doumas, Michalis [10 ]
Kolovou, Genovefa [11 ]
Lambadiari, Vaia [12 ,13 ]
Dima, Ioanna [2 ]
Kiouri, Estela [3 ]
Zacharis, Evangelos [4 ]
Agapakis, Dimitrios [14 ]
Attilakos, Achilleas [15 ]
Antza, Christina
Vlachopoulos, Charalambos [16 ]
Liberopoulos, Evangelos N. [1 ]
机构
[1] Univ Ioannina, Sch Med, Dept Internal Med, Ioannina, Greece
[2] Hippokrateion Hosp, Cardiol Clin, Athens, Greece
[3] Natl & Kapodistrian Univ Athens, Attikon Univ Gen Hosp, Sch Med, Dept Cardiol, Athens, Greece
[4] Univ Gen Hosp Herakl, Cardiol Clin, Iraklion, Greece
[5] Aristotle Univ Thessaloniki, Sch Med, AHEPA Hosp, Propaedeut Dept Internal Med 1, Thessaloniki, Greece
[6] Natl & Kapodistrian Univ Athens, Dept Pediat, Gen Childrens Hosp Pan & Aglaia Kyriakou, Med Sch,Pediat Clin B, Athens, Greece
[7] Police Med Ctr, Dept Endocrinol, Thessaloniki, Greece
[8] 424 Gen Mil Training Hosp, Dept Internal Med, Thessaloniki, Greece
[9] Aristotle Univ Thessaloniki, Med Sch, Papageorgiou Gen Hosp Thessaloniki, Dept Internal Med, Thessaloniki, Greece
[10] Aristotle Univ Thessaloniki, Med Sch, Hippokrat Gen Hosp, Dept Internal Med, Thessaloniki, Greece
[11] Metropolitan Hosp, LA Apheresis Unit, Cardiometabol Ctr, Lipid Clin, Athens, Greece
[12] Natl & Kapodistrian Univ Athens, Attikon Univ Gen Hosp, Propaedeut Internal Med Dept 2, Athens, Greece
[13] Natl & Kapodistrian Univ Athens, Attikon Univ Gen Hosp, Diabet Res Unit, Athens, Greece
[14] Dept Internal Med, Goumenissa, Greece
[15] Natl & Kapodistrian Univ Athens, Attikon Univ Gen Hosp, Dept Pediat, Med Sch,Pediat Clin C, Athens, Greece
[16] Natl & Kapodistrian Univ Athens, Sch Med, Hippokrat Gen Hosp, Dept Cardiol 1, Athens, Greece
关键词
Familial hypercholesterolemia; HELLAS FH registry; Low-density lipoprotein cholesterol; Hypolipidemic treatment; Target achievement; Proprotein convertase subtilisin/kexin type 9 inhibitors; CORONARY-ARTERY-DISEASE; HIGH-RISK; TREATMENT GOALS; REAL-LIFE; ALL-CAUSE; DIAGNOSIS; MORTALITY; GUIDANCE; STATINS;
D O I
10.1016/j.ijcard.2021.10.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The 2019 European guidelines (ESC/EAS) for the treatment of dyslipidaemias recommend more aggressive targets for low-density lipoprotein cholesterol (LDL-C) in patients with familial hypercholesterolemia (FH). Current lipid-lowering treatment is often inadequate to achieve these targets. Methods: Data from the HELLAS-FH registry were analysed to assess achievement of LDL-C targets in adults with FH based on the 2019 ESC/EAS guidelines. In patients who had not achieved LDL-C target, the maximally reduced LDL-C value was calculated after theoretical switch to rosuvastatin/ezetimibe 40/10 mg/day. The percentage of patients who remained candidates for proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) was then calculated. Results: Patients (n = 1694, mean age 50.8 +/- 14.7 years) had LDL-C levels 242 +/- 71 mg/dL (6.3 +/- 1.8 mmol/L) at diagnosis. Most treated patients were receiving statins (97.5%) and about half were on additional ezetimibe (47.5%). Based on the 2019 ESC/EAS guidelines the percentage of patients achieving LDL-C goals was only 2.7%. Following theoretical up titration to rosuvastatin/ezetimibe 40/10 mg, LDL-C target achievement rate would increase to 5.9%. In this scenario, most patients (55.9%) would be eligible for PCSK9i treatment. Following theoretical administration of a PCSK9i, LDL-C target achievement rate would rise to 57.6%. However, 42.4% of patients would still be eligible for further LDL-C lowering treatment. Conclusions: Most FH patients do not reach new LDL-C targets even if on maximum intensity statin/ezetimibe treatment. In this case, more than half of FH patients are candidates for PCSK9i therapy and a considerable proportion may still require additional LDL-C lowering.
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收藏
页码:119 / 124
页数:6
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