New lipid-lowering drugs: an update

被引:58
作者
Wierzbicki, A. S.
Hardman, T. C. [1 ]
Viljoen, A. [2 ]
机构
[1] Niche Sci & Technol, London, England
[2] Lister Hosp, Stevenage, Herts, England
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; CORONARY-HEART-DISEASE; APOLIPOPROTEIN-A-I; TRIGLYCERIDE TRANSFER PROTEIN; STATIN-TREATED PATIENTS; DOUBLE-BLIND; CARDIOVASCULAR EVENTS; PHOSPHOLIPASE A(2); LDL CHOLESTEROL; HDL CHOLESTEROL;
D O I
10.1111/j.1742-1241.2011.02867.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lipid lowering is established as a proven intervention to reduce atherosclerosis and its complications. Statins form the basis of care but are not able to treat all aspects of dyslipidaemia. Many novel therapeutic compounds are being developed. These include additional therapeutics for low-density lipoprotein cholesterol, for example, thyroid mimetics (thyroid receptor beta-agonists), antisense oligonucleotides or microsomal transfer protein inhibitors (MTPI); triglycerides, for example, novel peroxosimal proliferator activating receptors agonists, MTPIs, diacylglycerol acyl transferase-1 inhibitors and high-density lipoprotein cholesterol (HDL-C), for example, mimetic peptides; HDL delipidation strategies and cholesterol ester transfer protein inhibitors and modulators of inflammation, for example, phospholipase inhibitors. Gene therapy for specific rare disorders, for example, lipoprotein lipase deficiency using alipogene tiparvovec is also in clinical trials. Lipid-lowering drugs are likely to prove a fast-developing area for novel treatments as possible synergies exist between new and established compounds for the treatment of atherosclerosis.
引用
收藏
页码:270 / 280
页数:11
相关论文
共 133 条
[1]   Efficacy of apolipoprotein B synthesis inhibition in subjects with mild-to-moderate hyperlipidaemia [J].
Akdim, Fatima ;
Tribble, Diane L. ;
Flaim, JoAnn D. ;
Yu, Rosie ;
Su, John ;
Geary, Richard S. ;
Baker, Brenda F. ;
Fuhr, Rainard ;
Wedel, Mark K. ;
Kastelein, John J. P. .
EUROPEAN HEART JOURNAL, 2011, 32 (21) :2650-2659
[2]  
Al-Allaf Faisal A, 2010, Int Arch Med, V3, P36, DOI 10.1186/1755-7682-3-36
[3]  
Amgen, 2011, TIMI 57 DOUBL BLIND
[4]   The Emerging Risk Factors Collaboration: analysis of individual data on lipid, inflammatory and other markers in over 1.1 million participants in 104 prospective studies of cardiovascular diseases [J].
不详 .
EUROPEAN JOURNAL OF EPIDEMIOLOGY, 2007, 22 (12) :839-869
[5]  
[Anonymous], 1975, JAMA-J AM MED ASSOC, V231, P360
[6]  
Anthera Pharmaceuticals, 2011, VISTA 16 TRIAL EV SA
[7]  
Arisaph Pharmaceuticals, 2011, FDA ACC INV NEW DRUG
[8]   ApoB siRNA-induced Liver Steatosis is Resistant to Clearance by the Loss of Fatty Acid Transport Protein 5 (Fatp5) [J].
Ason, Brandon ;
Castro-Perez, Jose ;
Tep, Samnang ;
Stefanni, Alice ;
Tadin-Strapps, Marija ;
Roddy, Thomas ;
Hankemeier, Thomas ;
Hubbard, Brian ;
Sachs, Alan B. ;
Flanagan, W. Michael ;
Kuklin, Nelly A. ;
Mitnaul, Lyndon J. .
LIPIDS, 2011, 46 (11) :991-1003
[9]   Plasma PCSK9 Is Associated with Age, Sex, and Multiple Metabolic Markers in a Population-Based Sample of Children and Adolescents [J].
Baass, Alexis ;
Dubuc, Genevieve ;
Tremblay, Michel ;
Delvin, Edgard E. ;
O'Loughlin, Jennifer ;
Levy, Emile ;
Davignon, Jean ;
Lambert, Marie .
CLINICAL CHEMISTRY, 2009, 55 (09) :1637-1645
[10]   RVX-208 A Small Molecule That Increases Apolipoprotein A-I and High-Density Lipoprotein Cholesterol In Vitro and In Vivo [J].
Bailey, Dana ;
Jahagirdar, Ravi ;
Gordon, Allan ;
Hafiane, Anouar ;
Campbell, Steven ;
Chatur, Safia ;
Wagner, Gregory S. ;
Hansen, Henrik C. ;
Chiacchia, Fabrizio S. ;
Johansson, Jan ;
Krimbou, Larbi ;
Wong, Norman C. W. ;
Genest, Jacques .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 55 (23) :2580-2589