University of Washington School of Medicine, Cardiology Section Chief, Harborview Medical Center, Room 2CT-64, Box 359748, 325 Ninth Avenue, Seattle, WA 98104, USA.
Curr Cardiol Rep. 2009 Nov;11(6):452-9. doi: 10.1007/s11886-009-0065-1.
Although assessment of traditional coronary heart disease risk factors can often stratify individuals into low- or high-risk categories, additional means are needed to more precisely classify people clinically defined as intermediate-risk, to guide the intensity of risk-reducing therapies. The recognition that inflammatory pathways are important in the progression of atherosclerosis and its complications has prompted investigation to identify circulating risk markers that may be useful in risk stratification. This article summarizes recent studies on the current use of an emerging group of inflammatory markers: soluble CD-40 ligand, interleukin-18, myeloperoxidase, B-type natriuretic peptides, secretory phospholipase A(2), lipoprotein-associated phospholipase A(2), and C-reactive protein. The demonstration that lowering C-reactive protein along with low-density lipoprotein cholesterol with statins reduces events beyond cholesterol lowering alone suggests that titration of therapies using other emerging inflammatory markers may further reduce the toll of atherosclerosis in adult populations.
尽管评估传统的冠心病危险因素通常可以将个体分为低风险或高风险类别,但需要额外的方法来更准确地对临床上定义为中危的人群进行分类,以指导降低风险治疗的强度。认识到炎症途径在动脉粥样硬化及其并发症的进展中很重要,促使人们研究以确定可能有助于风险分层的循环风险标志物。本文总结了最近关于一组新兴炎症标志物的当前用途的研究:可溶性 CD40 配体、白细胞介素 18、髓过氧化物酶、B 型利钠肽、分泌型磷脂酶 A2、脂蛋白相关磷脂酶 A2 和 C 反应蛋白。他汀类药物降低 C 反应蛋白和低密度脂蛋白胆固醇的疗效表明,使用其他新兴炎症标志物调整治疗方案可能会进一步降低成年人群中动脉粥样硬化的危害。