Reduction of Low-Density Lipoprotein Cholesterol by Monoclonal Antibody Inhibition of PCSK9

被引:69
作者
Stein, Evan A. [1 ]
Raal, Frederick [2 ]
机构
[1] Univ Cincinnati, Dept Pathol & Lab Med, Cincinnati, OH 45221 USA
[2] Univ Witwatersrand, Dept Med, Fac Hlth Sci, ZA-2001 Johannesburg, South Africa
来源
ANNUAL REVIEW OF MEDICINE, VOL 65 | 2014年 / 65卷
关键词
LDL cholesterol; LDL receptors; monoclonal antibodies; SUBTILISIN/KEXIN TYPE 9; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; SERINE-PROTEASE; DOUBLE-BLIND; AMG; 145; EFFICACY; SAFETY; LDL; STATIN; MUTATIONS;
D O I
10.1146/annurev-med-022613-090402
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Published phase I and II trials with two fully human monoclonal antibodies to PCSK9 have provided comprehensive evidence that inhibiting PCSK9 is a very effective method to reduce low-density lipoprotein cholesterol (LDL-C). In all populations studied so far, whether on statins or LDL-C-reducing diet alone, with or without a genetic defect in the LDL receptor, and in subjects intolerant to statins, the LDL-C reductions have been large and consistent. Even the most efficacious statin, rosuvastatin, at its highest dose has not achieved such reductions. The clinical trials have established that monoclonal antibody therapy targeted to PCSK9 may be administered subcutaneously every two or four weeks. Current data suggest these drugs will provide an effective therapeutic option for LDL-C reduction and that, if proven safe in phase III trials, they will be as important to LDL-C control, and likely to cardiovascular disease risk reduction, as statins have been over the past three decades.
引用
收藏
页码:417 / 431
页数:15
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