Management of residual risk after statin therapy

被引:78
作者
Reith, Christina
Armitage, Jane [1 ]
机构
[1] Nuffield Dept Populat Hlth, Clin Trial Serv Unit, Richard Doll Bldg,Old Rd Campus,Roosevelt Dr, Oxford OX3 7LF, England
基金
英国医学研究理事会;
关键词
HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; CHOLESTEROL ABSORPTION INHIBITOR; TYPE-2; DIABETES-MELLITUS; COA REDUCTASE INHIBITORS; CORONARY-HEART-DISEASE; ESTER TRANSFER PROTEIN; B SYNTHESIS INHIBITOR; APOLIPOPROTEIN C-III; DOUBLE-BLIND; CARDIOVASCULAR EVENTS;
D O I
10.1016/j.atherosclerosis.2015.12.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular disease (CVD) is the leading cause of mortality worldwide. Observational data indicate that low-density lipoprotein cholesterol (LDL-C) levels are strongly positively associated with the risk of coronary heart disease (CHD) whilst the level of high-density lipoprotein cholesterol (HDL-C) is strongly inversely associated, with additional associations being observed for other lipid parameters such as triglycerides, apolipoproteins and lipoprotein(a) (Lp(a)). This has led to an interest in the development of a range of lipid intervention therapies. The most widely used of these interventions are statins, but even with intensive statin therapy some groups of patients remain at significant residual cardiovascular (CV) risk. In addition, some people are intolerant of statin therapy. In these circumstances, additional therapeutic agents may be needed. This review considers the evidence behind and the pros and cons of such additional agents. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:161 / 170
页数:10
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