New strategies for the development of lipid-lowering therapies to reduce cardiovascular risk

被引:18
作者
Graham, Ian [1 ]
Shear, Chuck [2 ]
De Graeff, Pieter [3 ,4 ]
Boulton, Caroline [5 ]
Catapano, Alberico L. [6 ]
Stough, Wendy Gattis [7 ,8 ]
Carlsson, Stefan C. [9 ]
De Backer, Guy [10 ]
Emmerich, Joseph [11 ]
Greenfeder, Scott [12 ]
Kim, Albert M. [13 ]
Lautsch, Dominik [14 ]
Nguyen, Tu [15 ]
Nissen, Steven E. [16 ]
Prasad, Krishna [17 ]
Ray, Kausik K. [18 ]
Robinson, Jennifer G. [19 ]
Sasiela, William J. [20 ]
Slot, Karsten Bruins [21 ]
Stroes, Erik [22 ]
Thuren, Tom [5 ]
Van der Schueren, Bart [23 ]
Velkovski-Rouyer, Maja [14 ]
Wasserman, Scott M. [24 ]
Wiklund, Olov [25 ]
Zouridakis, Emmanouil [17 ]
机构
[1] Tallaght Hosp, Adelaide Hlth Fdn, Trinity Coll, Dublin 24, Ireland
[2] Pfizer Inc, Global Prod Dev Internal Med, 235 E 42nd St, New York, NY 10017 USA
[3] Dutch Med Evaluat Board CBG MEB, Graadt Van Roggenweg 500, NL-3531 AH Utrecht, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Pharm & Clin Pharmacol, Hanzepl 1, NL-9713 GZ Groningen, Netherlands
[5] Novartis Pharma AG, Asklepios 8, CH-4056 Basel, Switzerland
[6] Univ Milan, IRCCS, Dept Pharmacol & Biomol Sci & Multimed, Via Balzaretti 9, I-20133 Milan, Italy
[7] Campbell Univ, Coll Pharm & Hlth Sci, Dept Clin Res, 217 Main St, Buies Creek, NC 27506 USA
[8] Campbell Univ, Coll Pharm & Hlth Sci, Dept Pharm Practice, 217 Main St, Buies Creek, NC 27506 USA
[9] AstraZeneca, Cardiovasc Pharmacol, Pepparredsleden 1, SE-43183 Molndal, Sweden
[10] Univ Ghent, Univ Hosp, Fac Med & Hlth Sci, Dept Publ Hlth, K3,4th Floor,De Pintelaan 185, B-9000 Ghent, Belgium
[11] Univ Paris 05, Cochin Hotel Dieu Hosp, French Natl Agcy Med & Hlth Prod Safety, 143-147 Blvd, F-93285 St Denis, France
[12] Daiichi Sankyo, Regulatory Affairs, 211 Mt Airy Rd, Basking Ridge, NJ 07920 USA
[13] Pfizer Inc, Internal Med Res Unit, 1 Portland St,4th Floor, Cambridge, MA 02139 USA
[14] Merck & Co Inc, 2000 Galloping Hill Rd, Kenilworth, NJ 07033 USA
[15] Sanofi, 55 Corp Dr, Bridgewater, NJ USA
[16] Cleveland Clin, Dept Cardiovasc Med, 9500 Euclid Ave, Cleveland, OH 44195 USA
[17] United Kingdom Med & Healthcare Prod Regulatory A, Licensing Div, 151 Buckingham Palace Rd, London SW1W 9SZ, England
[18] Imperial Coll, Dept Primary Care & Publ Hlth, Charing Cross Hosp, 323 Reynolds Bldg,Room 320, London W68RF, England
[19] Univ Iowa, Coll Publ Hlth, Dept Epidemiol, 145 N Riverside Dr S455 CPHB, Iowa City, IA 52242 USA
[20] Regeneron Pharmaceut, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
[21] Oslo Univ Hosp, Dept Med, Postboks 4956 Nydalen, N-0424 Oslo, Norway
[22] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[23] Univ Leuven, Lab Expt Med & Endocrinol, Herestr 49, B-3000 Leuven, Belgium
[24] Amgen Inc, One Amgen Ctr Dr,MS 38-2-C, Thousand Oaks, CA 91320 USA
[25] Sahlgrens Univ Hosp, Wallenberg Lab, S-41345 Gothenburg, Sweden
关键词
Dyslipidaemias; Clinical trials; Cardiovascular disease; Hypolipidaemic agents; DENSITY-LIPOPROTEIN CHOLESTEROL; ACUTE CORONARY SYNDROME; STATIN THERAPY; CLINICAL-TRIALS; MENDELIAN RANDOMIZATION; HEART-DISEASE; EVENTS; ATHEROSCLEROSIS; PROGRESSION; METAANALYSIS;
D O I
10.1093/ehjcvp/pvx031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The very high occurrence of cardiovascular events presents a major public health issue, because treatment remains suboptimal. Lowering LDL cholesterol (LDL-C) with statins or ezetimibe in combination with a statin reduces major adverse cardiovascular events. The cardiovascular risk reduction in relation to the absolute LDL-C reduction is linear for most interventions without evidence of attenuation or increase in risk at low LDL-C levels. Opportunities for innovation in dyslipidaemia treatment should address the substantial risk of lipid-associated cardiovascular events among patients optimally treated per guidelines but who cannot achieve LDL-C goals and who could benefit from additional LDL-C-lowering therapy or experience side effects of statins. Fresh approaches are needed to identify promising drug targets early and develop them efficiently. The Cardiovascular Round Table of the European Society of Cardiology (ESC) convened a workshop to discuss new lipid-lowering strategies for cardiovascular risk reduction. Opportunities to improve treatment approaches and the efficient study of new therapies were explored. Circulating biomarkers may not be fully reliable proxy indicators of the relationship between treatment effect and clinical outcome. Mendelian randomization studies may better inform development strategies and refine treatment targets before Phase 3. Trials should match the drug to appropriate lipid and patient profile, and guidelines may move towards a precision-based approach to individual patient management. Stakeholder collaboration is needed to ensure continued innovation and better international coordination of both regulatory aspects and guidelines. It should be noted that risk may also be addressed through increased attention to other risk factors such as smoking, hypertension, overweight, and inactivity.
引用
收藏
页码:119 / 127
页数:9
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