PCSK9 Inhibitors in Hyperlipidemia: Current Status and Clinical Outlook

被引:9
作者
Di Bartolo, Belinda [1 ]
Scherer, Daniel J. [1 ]
Brown, Alex [1 ]
Psaltis, Peter J. [1 ]
Nicholls, Stephen J. [1 ]
机构
[1] Univ Adelaide, South Australian Hlth & Med Res Inst, POB 11060, Adelaide, SA 5001, Australia
关键词
SUBTILISIN/KEXIN TYPE 9; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; HIGH CARDIOVASCULAR RISK; MONOCLONAL-ANTIBODY; RANDOMIZED-TRIAL; LDL CHOLESTEROL; LIPOPROTEIN METABOLISM; INTOLERANT PATIENTS; CORONARY-DISEASE; REDUCING LIPIDS;
D O I
10.1007/s40259-017-0220-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The clinical reality of residual risk despite statin (HMG-CoA reductase inhibitor) therapy and emergence of statin intolerance support the need to develop additional lipid-lowering strategies. Proprotein convertase subtilisin kexin type 9 (PCSK9) has received considerable attention by virtue of genetic and clinical studies that have revealed its pivotal role in the regulation of cholesterol homeostasis. Monoclonal antibodies have been developed targeting PCSK9, which have been demonstrated to produce profound low-density lipoprotein cholesterol (LDL-C) lowering when provided as monotherapy or in combination with statins. With the reports that the PCSK9 inhibitor evolocumab has a favorable impact on both plaque progression and cardiovascular outcomes, these findings begin to translate the benefits of PCSK9 inhibition from lipids to the vessel wall and ultimately to clinical outcomes. The clinical implications for the use of these agents are reviewed in this article.
引用
收藏
页码:167 / 174
页数:8
相关论文
共 55 条
[1]   Mutations in PCSK9 cause autosomal dominant hypercholesterolemia [J].
Abifadel, M ;
Varret, M ;
Rabès, JP ;
Allard, D ;
Ouguerram, K ;
Devillers, M ;
Cruaud, C ;
Benjannet, S ;
Wickham, L ;
Erlich, D ;
Derré, A ;
Villéger, L ;
Farnier, M ;
Beucler, I ;
Bruckert, E ;
Chambaz, J ;
Chanu, B ;
Lecerf, JM ;
Luc, G ;
Moulin, P ;
Weissenbach, J ;
Prat, A ;
Krempf, M ;
Junien, C ;
Seidah, NG ;
Boileau, C .
NATURE GENETICS, 2003, 34 (02) :154-156
[2]   Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials [J].
Baigent, C. ;
Blackwell, L. ;
Emberson, J. ;
Holland, L. E. ;
Reith, C. ;
Bhala, N. ;
Peto, R. ;
Barnes, E. H. ;
Keech, A. ;
Simes, J. ;
Collins, R. .
LANCET, 2010, 376 (9753) :1670-1681
[3]   Results of Bococizumab, A Monoclonal Antibody Against Proprotein Convertase Subtilisin/Kexin Type 9, from a Randomized, Placebo-Controlled, Dose-Ranging Study in Statin-Treated Subjects With Hypercholesterolemia [J].
Ballantyne, Christie M. ;
Neutel, Joel ;
Cropp, Anne ;
Duggan, William ;
Wang, Ellen Q. ;
Plowchalk, David ;
Sweeney, Kevin ;
Kaila, Nitin ;
Vincent, John ;
Bays, Harold .
AMERICAN JOURNAL OF CARDIOLOGY, 2015, 115 (09) :1212-1221
[4]  
Blackburn DF, 2005, CAN J CARDIOL, V21, P485
[5]   Familial Hypercholesterolemia [J].
Bouhairie, Victoria Enchia ;
Goldberg, Anne Carol .
CARDIOLOGY CLINICS, 2015, 33 (02) :169-+
[6]   The safety of therapeutic monoclonal antibodies: Implications for cardiovascular disease and targeting the PCSK9 pathway [J].
Catapano, A. L. ;
Papadopoulos, N. .
ATHEROSCLEROSIS, 2013, 228 (01) :18-28
[7]   A proprotein convertase subtilisin/kexin type 9 neutralizing antibody reduces serum cholesterol in mice and nonhuman primates [J].
Chan, Joyce C. Y. ;
Piper, Derek E. ;
Cao, Qiong ;
Liu, Dongming ;
King, Chadwick ;
Wang, Wei ;
Tang, Jie ;
Liu, Qiang ;
Higbee, Jared ;
Xia, Zhen ;
Di, Yongmei ;
Shetterly, Susan ;
Arimura, Ziva ;
Salomonis, Heather ;
Romanow, William G. ;
Thibault, Stephen T. ;
Zhang, Richard ;
Cao, Ping ;
Yang, Xiao-Ping ;
Yu, Timothy ;
Lu, Mei ;
Retter, Marc W. ;
Kwon, Gayle ;
Henne, Kirk ;
Pan, Oscar ;
Tsai, Mei-Mei ;
Fuchslocher, Bryna ;
Yang, Evelyn ;
Zhou, Lei ;
Lee, Ki Jeong ;
Daris, Mark ;
Sheng, Jackie ;
Wang, Yan ;
Shen, Wenyan D. ;
Yeh, Wen-Chen ;
Emery, Maurice ;
Walker, Nigel P. C. ;
Shan, Bei ;
Schwarz, Margrit ;
Jackson, Simon M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (24) :9820-9825
[8]   Predictors of adherence with antihypertensive and lipid-lowering therapy [J].
Chapman, RH ;
Benner, JS ;
Petrilla, AA ;
Tierce, JC ;
Collins, SR ;
Battleman, DS ;
Schwartz, JS .
ARCHIVES OF INTERNAL MEDICINE, 2005, 165 (10) :1147-1152
[9]   Sequence variations in PCSK9, low LDL, and protection against coronary heart disease [J].
Cohen, JC ;
Boerwinkle, E ;
Mosley, TH ;
Hobbs, HH .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (12) :1264-1272
[10]   Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia [J].
Cunningham, David ;
Danley, Dennis E. ;
Geoghegan, Kieran F. ;
Griffor, Matthew C. ;
Hawkins, Julie L. ;
Subashi, Timothy A. ;
Varghese, Alison H. ;
Ammirati, Mark J. ;
Culp, Jeffrey S. ;
Hoth, Lise R. ;
Mansour, Mahmoud N. ;
McGrath, Katherine M. ;
Seddon, Andrew P. ;
Shenolikar, Shirish ;
Stutzman-Engwall, Kim J. ;
Warren, Laurie C. ;
Xia, Donghui ;
Qiu, Xiayang .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (05) :413-419