Arterial stiffness improvement after adding on PCSK9 inhibitors or ezetimibe to high-intensity statins in patients with familial hypercholesterolemia: A Two-Lipid Center Real-World Experience

被引:34
作者
Mandraffino, Giuseppe [1 ]
Scicali, Roberto [2 ]
Rodriguez-Carrio, Javier [3 ,4 ,5 ]
Savarino, Francesca [1 ]
Mamone, Federica [1 ]
Scuruchi, Michele [1 ]
Cinquegrani, Maria [1 ]
Imbalzano, Egidio [1 ]
Di Pino, Antonino [2 ]
Piro, Salvatore [2 ]
Rabuazzo, Agata Maria [2 ]
Squadrito, Giovanni [1 ]
Purrello, Francesco [2 ]
Saitta, Antonino [1 ]
机构
[1] Univ Messina, Dept Clin & Expt Med, Messina, Italy
[2] Univ Catania, Dept Clin & Expt Med, Catania, Italy
[3] Univ Oviedo, Fac Med, Dept Funct Biol, Area Immunol, Oviedo, Spain
[4] Inst Invest Sanitaria Principado Asturias ISPA, Area Metab, Oviedo, Spain
[5] Hosp Univ Cent Asturias, Inst Reina Sofia Invest Nefrol, Bone & Mineral Res Unit, RED REN ISCIII, Oviedo, Spain
关键词
Familial hypercholesterolemia; PCSK9; inhibitors; Ezetimibe; Pulse wave velocity; LDL cholesterol; PULSE-WAVE VELOCITY; LDL-CHOLESTEROL; REDUCING LIPIDS; DOUBLE-BLIND; EFFICACY; SAFETY; ATHEROSCLEROSIS; POPULATION; THERAPY; PREVALENCE;
D O I
10.1016/j.jacl.2020.01.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Familial hypercholesterolemia (FH) is characterized by increased cardiovascular risk; despite-high intensity statins, only few patients with FH achieve the recommended low-density lipoprotein cholesterol (LDL C) targets. OBJECTIVE: We aimed to evaluate the effectiveness of six-month add-on therapy with proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9-i) or ezetimibe on lipid profile and pulse wave velocity (PWV) in patients with FH. METHODS: In this observational study, we evaluated 98 genetically confirmed patients with FH with an LDL-C off-target despite high-intensity statins with or without ezetimibe; of these, 53 patients (statin plus ezetimibe) added PCSK9-i (PCSK9-i group) and 45 (statin only) added ezetimibe (EZE group) per applicable guidelines and reimbursement rules. All patients obtained biochemical analysis and PWV evaluation at baseline and after six months of optimized treatment. RESULTS: After 6 months of add-on therapy, most patients achieving LDL-C targets were in the PCSK9-i group (77.3% PCSK9-i group vs 37.8% EZE group, P < .001). The PCSK9-i group achieved both a greater LDL-C and PWV reduction than the EZE group [-51% vs -22.8%, P < .001 and -15% vs -8.5%, P < .01, respectively]. In a linear regression analysis, we showed a coefficient (r) of 0.334 for the relationship between Delta PWV and Delta LDL (P < .05); moreover, in an exploratory analysis, the relationship appeared to be stronger in patients with FH without cardiovascular events (r = 0.422, P < .01). CONCLUSIONS: Lipid and PWV profiles in patients with FH significantly improved after addition of PCSK9-i or ezetimibe to high-intensity statin therapy; moreover, Delta PWV was associated with Delta LDL Our results are consistent with a beneficial role of these novel therapies in FH subjects. (C) 2020 National Lipid Association. All rights reserved.
引用
收藏
页码:231 / 240
页数:10
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