Understanding cardiac extracellular matrix remodeling to develop biomarkers of myocardial infarction outcomes

被引:102
|
作者
Nielsen, Signe Holm [1 ,2 ]
Mouton, Alan J. [3 ]
DeLeon-Pennell, Kristine Y. [3 ]
Genovese, Federica [1 ]
Karsdal, Morten [1 ]
Lindsey, Merry L. [3 ,4 ]
机构
[1] Nord Bioscie, Fibrosis Biol & Biomarkers, Herlev, Denmark
[2] Tech Univ Denmark, Dis Syst Immunol, Lyngby, Denmark
[3] Univ Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Heart Res, Jackson, MS 39216 USA
[4] GV Sonny Montgomery Vet Affairs Med Ctr, Jackson, MS USA
关键词
Extracellular matrix; Myocardial infarction; Biomarkers; Collagen; Matrix metalloproteinases; LEFT-VENTRICULAR DILATION; ALL-CAUSE MORTALITY; POSTMYOCARDIAL INFARCTION; HEART-FAILURE; BASEMENT-MEMBRANE; TISSUE INHIBITOR; CARDIOVASCULAR-DISEASE; DIASTOLIC DYSFUNCTION; HYPERTENSIVE PATIENTS; COLLAGEN DEPOSITION;
D O I
10.1016/j.matbio.2017.12.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cardiovascular Disease (CVD) is the most common cause of death in industrialized countries, and myocardial infarction (MI) is a major CVD with significant morbidity and mortality. Following MI, the left ventricle (LV) undergoes a wound healing response to ischemia that results in extracellular matrix (ECM) scar formation to replace necrotic myocytes. While ECM accumulation following MI is termed cardiac fibrosis, this is a generic term that does not differentiate between ECM accumulation that occurs in the infarct region to form a scar that is structurally necessary to preserve left ventricle (LV) wall integrity and ECM accumulation that increases LV wall stiffness to exacerbate dilation and stimulate the progression to heart failure. This review focuses on post-MI LV ECM remodeling, targeting the discussion on ECM biomarkers that could be useful for predicting MI outcomes. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 57
页数:15
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