Inflammatory markers in ST-elevation acute myocardial infarction

被引:91
|
作者
Seropian, Ignacio M. [1 ]
Sonnino, Chiara [2 ,3 ,4 ]
Van Tassell, Benjamin W. [2 ,3 ,5 ]
Biasucci, Luigi M. [4 ]
Abbate, Antonio [2 ,3 ]
机构
[1] Hosp Italiano Buenos Aires, Intervent Cardiol Dept, Buenos Aires, DF, Argentina
[2] Virginia Commonwealth Univ, VCU Pauley Heart Ctr, 1200 E Broad St,Box 980281, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Victoria Johnson Res Lab, Richmond, VA 23284 USA
[4] Catholic Univ, Dept Cardiovasc Med, Milan, Italy
[5] Virginia Commonwealth Univ, Sch Pharm, Richmond, VA 23284 USA
关键词
Inflammation; biological markers; ST-elevation acute myocardial infarction; ventricular remodeling; C-REACTIVE PROTEIN; CELL DISTRIBUTION WIDTH; PERCUTANEOUS CORONARY INTERVENTION; ENDOTHELIAL PROGENITOR CELLS; MIGRATION INHIBITORY FACTOR; LONG-TERM MORTALITY; PLASMA ADIPONECTIN LEVELS; LEFT-VENTRICULAR FUNCTION; MONOCYTE CHEMOATTRACTANT PROTEIN-1; INTERCELLULAR-ADHESION MOLECULE-1;
D O I
10.1177/2048872615568965
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
After acute myocardial infarction, ventricular remodeling is characterized by changes at the molecular, structural, geometrical and functional level that determine progression to heart failure. Inflammation plays a key role in wound healing and scar formation, affecting ventricular remodeling. Several, rather different, components of the inflammatory response were studied as biomarkers in ST-elevation acute myocardial infarction. Widely available and inexpensive tests, such as leukocyte count at admission, as well as more sophisticated immunoassays provide powerful predictors of adverse outcome in patients with ST-elevation acute myocardial infarction. We review the value of inflammatory markers in ST-elevation acute myocardial infarction and their association with ventricular remodeling, heart failure and sudden death. In conclusion, the use of these biomarkers may identify subjects at greater risk of adverse events and perhaps provide an insight into the mechanisms of disease progression.
引用
收藏
页码:382 / 395
页数:14
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