Atherosclerosis: Recent trials, new targets and future directions

被引:28
作者
Ladeiras-Lopes, Ricardo [1 ,2 ]
Agewall, Stefan [3 ,4 ]
Tawakol, Ahmed [5 ,6 ]
Staels, Bart [7 ]
Stein, Evan [8 ]
Mentz, Robert J. [9 ,10 ]
Leite-Moreira, Adelino [1 ]
Zannad, Faiez [11 ]
Koenig, Wolfgang [12 ,13 ,14 ]
机构
[1] Univ Porto, Fac Med, Cardiovasc Res & Dev Ctr, Dept Physiol & Cardiothorac Surg, Oporto, Portugal
[2] Gaia Espinho Hosp Ctr, Dept Cardiol, Vila Nova De Gaia, Portugal
[3] Univ Oslo, Oslo Univ Hosp Ulleval, Dept Cardiol, Oslo, Norway
[4] Univ Oslo, Inst Clin Med, Oslo, Norway
[5] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
[6] Harvard Univ, Sch Med, Div Cardiol, Boston, MA USA
[7] Univ Lille 2, INSERM, EGID, Inst Pasteur Lille,UMR1011, Lille, France
[8] Metab & Atherosclerosis Res Ctr, Cincinnati, OH USA
[9] Duke Univ Hosp, Duke Clin Res Inst, Durham, NC USA
[10] Duke Univ Hosp, Div Cardiol, Durham, NC USA
[11] Univ Lorraine, Ctr Invest Clin 9501, INSERM, Nancy, France
[12] Univ Ulm, Med Ctr, Dept Internal Med Cardiol 2, D-89069 Ulm, Germany
[13] Tech Univ Munich, Deutsch Herzzentrum Munchen, D-80290 Munich, Germany
[14] German Ctr Cardiovasc Res, DZHK, Partner Site Munich Heart Alliance, Munich, Germany
关键词
Atherosclerosis; Pharmacology; Clinical research; DENSITY-LIPOPROTEIN CHOLESTEROL; TRIGLYCERIDE TRANSFER PROTEIN; SUBTILISIN/KEXIN TYPE 9; ACUTE CORONARY SYNDROME; APOLIPOPROTEIN-A-I; ESTER TRANSFER PROTEIN; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; SECRETORY PHOSPHOLIPASE A(2); STATIN-TREATED PATIENTS; RESIDUAL VASCULAR RISK;
D O I
10.1016/j.ijcard.2015.05.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mortality from cardiovascular diseases (CVD) represents the primary cause of death worldwide. Prevention or treatment of atherosclerosis and its clinical sequelae is a central goal in the management of patients with established vascular disease or those at high-risk for vascular events. This paper provides a review of the contemporary pharmacological armamentarium targeting atherosclerosis and also highlights strategies to support future clinical trial design. Powering future trials targeting LDL-cholesterol to its absolute reduction and including patients with a higher LDL-C despite optimal medical therapy (or unable to tolerate statins) will increase the odds of meaningful results. Mendelian randomization studies may identify new causal risk factors for CVD that would help in the selection of the patients most likely to benefit from a specific new compound. Furthermore, imaging techniques integrating a morphological and functional assessment such as IVUS, OCT, PET/CT and PET/MRI may represent in a near future robust "soft" endpoints to support successful translation of early research into meaningful phase III clinical outcome trials. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:72 / 81
页数:10
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