A call to action for new global approaches to cardiovascular disease drug solutions

被引:30
作者
Figtree, Gemma A. [1 ]
Broadfoot, Keith [2 ]
Casadei, Barbara [3 ,4 ,5 ]
Califf, Robert [6 ]
Crea, Filippo [7 ]
Drummond, Grant R. [8 ,9 ]
Freedman, Jane E. [10 ]
Guzik, Tomasz J. [11 ,12 ]
Harrison, David [13 ]
Hausenloy, Derek J. [14 ,15 ,16 ,17 ,18 ]
Hill, Joseph A. [19 ]
Januzzi, James L. [20 ]
Kingwell, Bronwyn A. [21 ]
Lam, Carolyn S. P. [22 ,23 ]
MacRae, Calum A. [24 ]
Misselwitz, Frank [25 ]
Miura, Tetsuji [26 ]
Ritchie, Rebecca H. [27 ]
Tomaszewski, Maciej [28 ,29 ]
Wu, Joseph C. [30 ]
Xiao, Junjie [31 ]
Zannad, Faiez [32 ]
机构
[1] Univ Sydney, Royal North Shore Hosp, Kolling Inst, Sydney, NSW, Australia
[2] Natl Heart Fdn Australia, Clin Comm, Melbourne, Vic, Australia
[3] Univ Oxford, Radcliffe Dept Med, Div Cardiovasc Med, Oxford, England
[4] NIHR Oxford Biomed Res Ctr, Oxford, England
[5] British Heart Fdn Ctr Res Excellence, Oxford, England
[6] Verily, San Francisco, CA USA
[7] Catholic Univ, Rome, Italy
[8] La Trobe Univ, Ctr Cardiovasc Biol & Dis Res, Melbourne, Vic, Australia
[9] La Trobe Univ, Dept Physiol Anat & Microbiol, Melbourne, Vic, Australia
[10] Univ Massachusetts, Med Sch, Cardiovasc Res, Amherst, MA 01003 USA
[11] Univ Glasgow, Inst Cardiovasc & Med Sci, Glasgow, Lanark, Scotland
[12] Jagiellonian Univ, Coll Med, Krakow, Poland
[13] Vanderbilt Univ, Sch Med, Clin Pharmacol, Nashville, TN 37212 USA
[14] Duke Natl Univ Singapore, Signat Res Program, NUS Med Sch, Cardiovasc & Metab Disorders Program, Singapore, Singapore
[15] Natl Heart Ctr, Natl Heart Res Inst Singapore, Singapore, Singapore
[16] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore, Singapore
[17] UCL, Hatter Cardiovasc Inst, London, England
[18] Asia Univ, Coll Med & Hlth Sci, Cardiovasc Res Ctr, Taichung, Taiwan
[19] Univ Texas Southwestern, Dallas, TX USA
[20] Harvard Univ, Massachusetts Gen Hosp, Boston, MA 02115 USA
[21] CSL Ltd, Melbourne, Vic, Australia
[22] Natl Heart Ctr Singapore, Singapore, Singapore
[23] Duke Natl Univ Singapore, Singapore, Singapore
[24] Harvard Med Sch, Brigham & Womens Hosp, Boston, MA 02115 USA
[25] Bayer AG, Pharmaceut Div, Wuppertal, Germany
[26] Sapporo Med Univ, Dept Cardiovasc Renal & Metab Med, Sapporo, Hokkaido, Japan
[27] Monash Univ, Drug Discovery Biol, Monash Inst Pharmaceut Sci, Parkville Campus, Parkville, Vic, Australia
[28] Univ Manchester, Div Cardiovasc Sci, Fac Biol Med & Hlth, Manchester, Lancs, England
[29] Univ Manchester, Manchester Univ NHS Fdn Trust, Manchester, Lancs, England
[30] Stanford Cardiovasc Inst, Stanford, CA USA
[31] Shanghai Univ, Sch Life Sci, Inst Cardiovasc Sci, Cardiac Regenerat & Ageing Lab, Shanghai 200444, Peoples R China
[32] Univ Lorraine, CHRU Nancy, INI CRCT, INSERM CIC 1493, Nancy, France
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Therapeutic target; Drug discovery; Precision medicine; Multi-omics; Atherosclerosis; Heart failure; Pharmacotherapy; Cardiovascular; Organoids; ACUTE CORONARY SYNDROMES; HEART-FAILURE; GUIDELINES; THERAPIES; MODELS; CRISIS;
D O I
10.1093/eurheartj/ehab068
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Whilst we continue to wrestle with the immense challenge of implementing equitable access to established evidence-based treatments, substantial gaps remain in our pharmacotherapy armament for common forms of cardiovascular disease including coronary and peripheral arterial disease, heart failure, hypertension, and arrhythmia. We need to continue to invest in the development of new approaches for the discovery, rigorous assessment, and implementation of new therapies. Currently, the time and cost to progress from lead compound/product identification to the clinic, and the success rate in getting there reduces the incentive for industry to invest, despite the enormous burden of disease and potential size of market. There are tremendous opportunities with improved phenotyping of patients currently batched together in syndromic 'buckets'. Use of advanced imaging and molecular markers may allow stratification of patients in a manner more aligned to biological mechanisms that can, in turn, be targeted by specific approaches developed using high-throughput molecular technologies. Unbiased 'omic' approaches enhance the possibility of discovering completely new mechanisms in such groups. Furthermore, advances in drug discovery platforms, and models to study efficacy and toxicity more relevant to the human disease, are valuable. Reimagining the relationships among discovery, translation, evaluation, and implementation will help reverse the trend away from investment in the cardiovascular space, establishing innovative platforms and approaches across the full spectrum of therapeutic development.
引用
收藏
页码:1464 / 1475
页数:12
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