Anacetrapib for the treatment of dyslipidaemia: the last bastion of the cholesteryl ester transfer protein inhibitors?

被引:8
|
作者
Page, Michael M. [1 ,2 ]
Hooper, Amanda J. [1 ,2 ,3 ,4 ]
Burnett, John R. [1 ,2 ,3 ]
机构
[1] Royal Perth Hosp, Dept Clin Biochem, PathWest Lab Med WA, Perth, WA 6001, Australia
[2] Fiona Stanley Hosp Network, Perth, WA, Australia
[3] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
[4] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA 6009, Australia
关键词
Anacetrapib; apolipoprotein A-I; atherosclerosis; cardiovascular disease; cholesteryl ester transfer protein inhibitors; high density lipoprotein; low density lipoprotein; HIGH-DENSITY-LIPOPROTEIN; CORONARY-HEART-DISEASE; CARDIOVASCULAR-RISK; HEALTHY-SUBJECTS; CETP INHIBITOR; FAMILIAL HYPERCHOLESTEROLEMIA; EFFECTIVE STRATEGY; APOLIPOPROTEIN-B; REDUCING LIPIDS; STATIN THERAPY;
D O I
10.1517/14656566.2016.1129402
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Inhibition of cholesteryl ester transfer protein (CETP) has emerged as a potential way to decrease cardiovascular risk by raising high density lipoprotein (HDL) cholesterol and lowering low density lipoprotein (LDL) cholesterol concentrations. However, high profile withdrawals of several CETP inhibitors have cast doubt over this hypothesis. Despite this concern, anacetrapib appears to be safe, well-tolerated and delivers a substantial increases in HDL cholesterol and reductions in LDL cholesterol as monotherapy and when combined with a statin.Areas covered: We discuss the role of CETP and HDL cholesterol as therapeutic targets, describe the pharmacokinetics and pharmacodynamics of anacetrapib, as well as report on the recent clinical trials.Expert opinion: The focus of CETP inhibition has shifted from HDL cholesterol-raising to LDL cholesterol-lowering. Although anacetrapib appears to be safe and is effective in altering lipid-related biochemical parameters of interest, its effect on cardiovascular outcomes remains unknown. Extrapolation of LDL cholesterol lowering to improved cardiovascular outcomes is not possible, because LDL and HDL functionality in the setting of anacetrapib treatment is unclear. The results of the phase III REVEAL randomised controlled trial will be critical for anacetrapib to establish a place in clinical care.
引用
收藏
页码:275 / 281
页数:7
相关论文
共 50 条
  • [31] Biochemical characterization of cholesteryl ester transfer protein inhibitors
    Ranalletta, Mollie
    Bierilo, Kathleen K.
    Chen, Ying
    Milot, Denise
    Chen, Qing
    Tung, Elaine
    Houde, Caroline
    Elowe, Nadine H.
    Garcia-Calvo, Margarita
    Porter, Gene
    Eveland, Suzanne
    Frantz-Wattley, Betsy
    Kavana, Mike
    Addona, George
    Sinclair, Peter
    Sparrow, Carl
    O'Neill, Edward A.
    Koblan, Ken S.
    Sitlani, Ayesha
    Hubbard, Brian
    Fisher, Timothy S.
    [J]. JOURNAL OF LIPID RESEARCH, 2010, 51 (09) : 2739 - 2752
  • [32] How Anacetrapib Inhibits the Activity of the Cholesteryl Ester Transfer Protein? Perspective through Atomistic Simulations
    Aijanen, Tarja
    Koivuniemi, Artturi
    Javanainenl, Matti
    Rissanen, Sami
    Rog, Tomasz
    Vattulainent, Ilpo
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2014, 10 (11)
  • [33] Phosphonate-containing analogs of cholesteryl ester as novel inhibitors of cholesteryl ester transfer protein
    Pietzonka, T
    Damon, R
    Russell, M
    Wattanasin, S
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (16) : 1951 - 1954
  • [34] Changes in LDL particle concentrations after treatment with the cholesteryl ester transfer protein inhibitor anacetrapib alone or in combination with atorvastatin
    Krauss, Ronald M.
    Pinto, Cathy Anne
    Liu, Yang
    Johnson-Levonas, Amy O.
    Dansky, Hayes M.
    [J]. JOURNAL OF CLINICAL LIPIDOLOGY, 2015, 9 (01) : 93 - 102
  • [35] Cholesteryl Ester Transfer Protein Inhibition With Anacetrapib Decreases Fractional Clearance Rates of High-Density Lipoprotein Apolipoprotein A-I and Plasma Cholesteryl Ester Transfer Protein
    Reyes-Soffer, Gissette
    Millar, John S.
    Ngai, Colleen
    Jumes, Patricia
    Coromilas, Ellie
    Asztalos, Bela
    Johnson-Levonas, Amy O.
    Wagner, John A.
    Donovan, Daniel S.
    Karmally, Wahida
    Ramakrishnan, Rajasekhar
    Holleran, Stephen
    Thomas, Tiffany
    Dunbar, Richard L.
    deGoma, Emil M.
    Rafeek, Hashmi
    Baer, Amanda L.
    Liu, Yang
    Lassman, Michael E.
    Gutstein, David E.
    Rader, Daniel J.
    Ginsberg, Henry N.
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2016, 36 (05) : 994 - 1002
  • [36] Inhibitors of cholesteryl ester transfer protein - a step forward in the treatment of coronary artery disease?
    Doggrell, SA
    [J]. DRUGS OF THE FUTURE, 2005, 30 (01) : 45 - 50
  • [37] Cholesteryl Ester Transfer Protein Penetrates Lipoproteins For Cholesteryl Ester Transfer
    Ren, Gang
    Zhang, Shengli
    Cavigiolio, Giorgio
    Lei, Dongsheng
    Oda, Michael
    Weisgraber, Karl H.
    Rye, Kerry-Anne
    Pownall, Henry J.
    Qiu, Xiayang
    [J]. BIOPHYSICAL JOURNAL, 2010, 98 (03) : 36A - 36A
  • [38] Review of the quantitative analysis of cholesteryl ester transfer protein inhibitors
    Mullangi, Ramesh
    Srinivas, Nuggehally R.
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2013, 27 (10) : 1259 - 1272
  • [39] Antisense Inhibition of Cholesteryl Ester Transfer Protein Increases HDL Cholesterol Comparable to Anacetrapib in Transgenic Mice
    Bell, Thomas A.
    Graham, Mark
    Lee, Richard
    Mullick, Adam
    Fu, Wuxia
    Crooke, Rosanne
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2010, 30 (11) : E212 - E212
  • [40] Do Cholesteryl Ester Transfer Protein Inhibitors Have a Role in the Treatment of Cardiovascular Disease?
    Nicholls, Stephen J.
    Nelson, Adam J.
    [J]. AMERICAN JOURNAL OF CARDIOVASCULAR DRUGS, 2019, 19 (03) : 229 - 235