Anti-Inflammatory Drugs in Patients with Ischemic Heart Disease

被引:7
|
作者
Pello Lazaro, Ana Maria [1 ,2 ]
Blanco-Colio, Luis M. [3 ,4 ]
Franco Pelaez, Juan Antonio [1 ,2 ]
Tunon, Jose [1 ,2 ,3 ,4 ]
机构
[1] IIS Fdn Jimenez Diaz, Dept Cardiol, Madrid 28040, Spain
[2] Univ Autonoma Madrid, Dept Med, Madrid 28029, Spain
[3] IIS Fdn Jimenez Diaz, Lab Vasc Pathol, Madrid 28040, Spain
[4] CIBERCV, Madrid 28029, Spain
关键词
inflammation; atherosclerosis; coronary heart disease; biomarkers; MONOCYTE CHEMOATTRACTANT PROTEIN-1; FACTOR-KAPPA-B; INTERCELLULAR-ADHESION MOLECULE-1; CORONARY ATHEROSCLEROTIC PLAQUES; PHOSPHOLIPASE A(2); GASTROINTESTINAL TOXICITY; MACROPHAGE INFILTRATION; CARDIOVASCULAR-DISEASE; POTENTIAL IMPLICATIONS; MYOCARDIAL-INFARCTION;
D O I
10.3390/jcm10132835
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inflammation has long been known to play a role in atherogenesis and plaque complication, as well as in some drugs used in therapy for atherosclerotic disease, such as statins, acetylsalicylic acid, and modulators of the renin-angiotensin system, which also have anti-inflammatory effects. Furthermore, inflammatory biomarkers have been demonstrated to predict the incidence of cardiovascular events. In spite of this, and with the exception of acetylsalicylic acid, non-steroidal anti-inflammatory drugs are unable to decrease the incidence of cardiovascular events and may even be harmful to the cardiovascular system. In recent years, other anti-inflammatory drugs, such as canakinumab and colchicine, have shown an ability to reduce the incidence of cardiovascular events in secondary prevention. Colchicine could be a potential candidate for use in clinical practice given its safety and low price, although the results of temporary studies require confirmation in large randomized clinical trials. In this paper, we discuss the evidence linking inflammation with atherosclerosis and review the results from various clinical trials performed with anti-inflammatory drugs. We also discuss the potential use of these drugs in routine clinical settings.
引用
收藏
页数:15
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