Molecular imaging of cardiac remodelling after myocardial infarction

被引:107
作者
Curley, Daniel [1 ]
Plaza, Begona Lavin [2 ,4 ]
Shah, Ajay M. [3 ,4 ]
Botnar, Rene M. [2 ,4 ,5 ]
机构
[1] Kings Coll London, GKT Sch Med, London, England
[2] Kings Coll London, Sch Biomed Engn & Imaging Sci, St Thomas Hosp, 4th Floor,Lambeth Wing, London SE1 7EH, England
[3] Kings Coll London, Sch Cardiovasc Med & Sci, London, England
[4] Kings Coll London, British Heart Fdn, Ctr Excellence, London, England
[5] Pontificia Univ Catolica Chile, Escuela Ingn, Santiago, Chile
基金
英国惠康基金; 英国工程与自然科学研究理事会;
关键词
Myocardial infarction; Cardiac remodelling; Cardiovascular imaging; MRI; ANGIOTENSIN-CONVERTING ENZYME; POSITRON-EMISSION-TOMOGRAPHY; MITOCHONDRIAL PERMEABILITY TRANSITION; ALPHA(V)BETA(3) INTEGRIN EXPRESSION; ENDOTHELIAL GROWTH-FACTOR; CORONARY-ARTERY-DISEASE; ISCHEMIC CELL-DEATH; MAGNETIC-RESONANCE; IN-VIVO; REOXYGENATED CARDIOMYOCYTES;
D O I
10.1007/s00395-018-0668-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myocardial infarction and subsequent heart failure is a major health burden associated with significant mortality and morbidity in western societies. The ability of cardiac tissue to recover after myocardial infarction is affected by numerous complex cellular and molecular pathways. Unbalance or failure of these pathways can lead to adverse remodelling of the heart and poor prognosis. Current clinical cardiac imaging modalities assess anatomy, perfusion, function, and viability of the myocardium, yet do not offer any insight into the specific molecular pathways involved in the repair process. Novel imaging techniques allow visualisation of these molecular processes and may have significant diagnostic and prognostic values, which could aid clinical management. Single photon-emission tomography, positron-emission tomography, and magnetic resonance imaging are used to visualise various aspects of these molecular processes. Imaging probes are usually attached to radioisotopes or paramagnetic nanoparticles to specifically target biological processes such as: apoptosis, necrosis, inflammation, angiogenesis, and scar formation. Although the results from preclinical studies are promising, translating this work to a clinical environment in a valuable and cost-effective way is extremely challenging. Extensive evaluation evidence of diagnostic and prognostic values in multi-centre clinical trials is still required.
引用
收藏
页数:18
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