Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) inhibitors and the risk for neurocognitive adverse events: A systematic review, meta-analysis and meta-regression

被引:13
|
作者
Raccah, Bruria Hirsh [1 ,2 ]
Yanovsky, Alona [1 ]
Treves, Nir [1 ]
Rotshild, Victoria [1 ]
Renoux, Christel [3 ,4 ]
Danenberg, Haim [2 ]
Eliaz, Ran [2 ]
Matok, Ilan [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Pharm, Fac Med, Div Clin Pharm,Inst Drug Res, Jerusalem, Israel
[2] Hadassah Univ Hosp, Dept Cardiol, Jerusalem, Israel
[3] Jewish Gen Hosp, Ctr Clin Epidemiol, Lady Davis Inst, Dept Epidemiol, Montreal, PQ, Canada
[4] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ, Canada
关键词
PCSK9; inhibitors; Neurocognitive adverse events; HIGH CARDIOVASCULAR-RISK; RANDOMIZED-TRIAL; CHOLESTEROL LEVELS; LDL-CHOLESTEROL; CORONARY EVENTS; REDUCING LIPIDS; ADD-ON; ALIROCUMAB; EFFICACY; SAFETY;
D O I
10.1016/j.ijcard.2021.04.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: It has been suggested that lipid lowering therapy causes impaired cognitive changes. The association between the use of Proprotein Convertase Subtilisin/ Kexin Type 9 (PCSK9) inhibitors and the risk of neurocognitive adverse events remains unclear. This meta-analysis aims to assess neurocognitive safety of PCSK9 inhibitors in randomized controlled trials (RCTs). Methods and results: The research was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). PubMed (MEDLINE), Embase and Cochrane library were searched through September 2019. Selection criteria included RCTs that addressed to neurocognitive adverse events of participants using Alirocumab, Evolocumab or Bococizumab, with a follow up duration of at least 6 months. The search results were screened by two independent reviewers. Safety data from included papers were extracted. Random effects meta-analysis was used to pool results, and meta-regression was utilized when applicable. Twenty-one studies were included. Among 59,733 patients, 31,611 were treated with PCSK9 inhibitors. The follow-up period ranged from 24 weeks to 48 months. No significant difference in the incidence of neurocognitive adverse effects between the groups was identified (RR = 1.01, 95% CI: 0.86-1.19, I-2 = 3%). Similar results were seen in subgroup analysis for each of the medications (alirocumab-RR - 0.88, 95% CI: 0.72-1.08, I-2 = 0%, evolocumab- RR = 1.42, 95% CI: 0.74-2.73, I-2 = 55%). Ameta-regression analysis for evolocumab revealed that prolonged study durationwas associated with decreased risk for neurocognitive adverse events (beta week = -0.0037, p-value = 0.03). Conclusions: Pooled results of our meta-analysis and meta-regression show that exposure to PCSK9 inhibitors is not associated with an increased risk of neurocognitive adverse effects. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 50 条
  • [31] Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) and Its Inhibitors: a Review of Physiology, Biology, and Clinical Data
    Durairaj A.
    Sabates A.
    Nieves J.
    Moraes B.
    Baum S.
    Current Treatment Options in Cardiovascular Medicine, 2017, 19 (8)
  • [32] Association of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) With Cardiovascular Risk in Primary Prevention
    Zhu, Yiming M.
    Anderson, Todd J.
    Sikdar, Khokan
    Fung, Marinda
    McQueen, Matthew J.
    Lonn, Eva M.
    Verma, Subodh
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2015, 35 (10) : 2254 - 2259
  • [33] Effects of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibition with Bococizumab on Lipoprotein Particles in Hypercholesterolemic Subjects
    Wan, Hong
    Gumbiner, Barry
    Joh, Tenshang
    Riel, Tom
    Udata, Chandrasekhar
    Forgues, Philippe
    Garzone, Pamela D.
    CLINICAL THERAPEUTICS, 2017, 39 (11) : 2243 - 2259
  • [34] Proprotein Convertase Subtilisin Kexin 9 (PCSK9) Inhibitors in the Treatment of Hypercholesterolemia and other Pathologies
    Seidah, Nabil G.
    CURRENT PHARMACEUTICAL DESIGN, 2013, 19 (17) : 3161 - 3172
  • [35] Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors: A Brief Overview
    Noel, Zachary R.
    Beavers, Craig J.
    AMERICAN JOURNAL OF MEDICINE, 2017, 130 (02) : 229.e1 - 229.e4
  • [36] Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibitors, Reality or Dream in Managing Patients with Cardiovascular Disease
    Alkhalil, Mohammad
    CURRENT DRUG METABOLISM, 2019, 20 (01) : 72 - 82
  • [37] Treatment with Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibitors to Reduce Cardiovascular Inflammation and Outcomes
    Liberale, Luca
    Montecucco, Fabrizio
    Camici, Giovanni G.
    Dallegri, Franco
    Vecchie, Alessandra
    Carbone, Federico
    Bonaventura, Aldo
    CURRENT MEDICINAL CHEMISTRY, 2017, 24 (14) : 1403 - 1416
  • [38] Efficacy and safety of different proprotein convertase subtilisin/kexin type 9 inhibitors in patients with hypercholesterolemia at high cardiovascular risk: a systematic review and meta-analysis
    MU Guang-yan
    XIANG Qian
    ZHOU Shuang
    LIU Zhi-yan
    QI Li-tong
    JIANG Jie
    GONG Yan-jun
    XIE Qiu-fen
    WANG Zi-ning
    ZHANG Han-xu
    HUO Yong
    CUI Yi-min
    中国药理学与毒理学杂志, 2019, (10) : 791 - 791
  • [39] Pro protein convertase subtilisin kexin type 9 (PCSK9) inhibitors Pharmacological review and update
    Corral, Pablo
    Suter, Agustina
    Rusconi, Alejandro
    Trigo, Leandro
    INSUFICIENCIA CARDIACA, 2016, 11 (03) : 122 - 129
  • [40] Proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors: Shaping the future after the further cardiovascular outcomes research with PCSK9 inhibition in subjects with elevated risk (FOURIER) trial
    Katsiki, Niki
    Athyros, Vasilios G.
    Mikhailidis, Dimitri P.
    Mantzoros, Christos
    METABOLISM-CLINICAL AND EXPERIMENTAL, 2017, 74 : 43 - 46