Novel anti-inflammatory strategies in atherosclerosis

被引:43
作者
van der Valk, Fleur M. [1 ]
van Wijk, Diederik F. [1 ]
Stroes, Erik S. G. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
关键词
anti-inflammatory strategies; atherosclerosis; cardiovascular imaging; vessel wall inflammation; CORONARY-HEART-DISEASE; MONOCYTE CHEMOATTRACTANT PROTEIN-1; SECRETORY PHOSPHOLIPASE A(2); CAROTID PLAQUE INFLAMMATION; C-REACTIVE-PROTEIN; RHEUMATOID-ARTHRITIS; MYOCARDIAL-INFARCTION; IN-VIVO; DOUBLE-BLIND; VASCULAR INFLAMMATION;
D O I
10.1097/MOL.0b013e3283587543
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
Purpose of review Inflammation has been widely acknowledged to contribute throughout all stages of atherogenesis. However, these recent advances in our understanding have not been translated into clinical practice in which the mainstay of treatment is still lipid-targeted therapy. This review provides an overview of promising anti-inflammatory therapies in atherosclerosis, and discusses potential drawbacks and clinical benefits. Recent findings Immunosuppressive drugs are likely to beneficially affect atherogenesis. Several novel anti-inflammatory targets have been scrutinized, of which some have reached clinical development stage, such as cytokine targets interleukin-1 and interleukin-6, CCR2 antagonist, selective phospholipase, and leukotriene inhibitors. Novel imaging modalities such as MRI and PET-computed tomography provide valuable surrogate inflammatory endpoints for risk stratification and testing anti-inflammatory agents in cardiovascular randomized trials. Summary Anti-inflammatory therapies hold great promise in cardiovascular prevention regimens; however, atherosclerosis is a chronic disease, and systemic long-term use of anti-inflammatory agents carries the risk of complications arising from immunosuppression. In order to successfully add immunosuppressive drugs to our routine armament, we need to identify high-risk patients who benefit from anti-inflammatory treatment, increase our insight into the inflammatory pathogenesis of atherogenesis, and find safe and effective compounds capable of directly suppressing plaque inflammation.
引用
收藏
页码:532 / 539
页数:8
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