Case reports of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibition nonresponse

被引:8
作者
Saeed, Anum [1 ,2 ]
Virani, Salim S. [1 ,2 ,3 ,4 ,5 ]
Jones, Peter H. [1 ]
Ballantyne, Christie M. [1 ,2 ,6 ]
Nambi, Vijay [1 ,2 ,3 ,6 ]
机构
[1] Baylor Coll Med, Dept Med, Sect Cardiovasc Res, Houston, TX 77030 USA
[2] Methodist DeBakey Heart & Vasc Ctr, Ctr Cardiovasc Dis Prevent, Houston, TX USA
[3] Michael E DeBakey VA Med Ctr, Cardiol Sect, Houston, TX USA
[4] Michael E DeBakey VA Med Ctr, Hlth Serv Res & Dev Ctr Innovat, Hlth Policy Qual & Informat Program, Houston, TX USA
[5] Baylor Coll Med, Dept Med, Sect Hlth Serv Res, Houston, TX 77030 USA
[6] Baylor Coll Med, Dept Med, Sect Cardiol, Houston, TX 77030 USA
关键词
Coronary artery disease; Cardiovascular diseases; Dyslipidemia; Hypercholesterolemia; PCSK9; inhibitors; AUTOSOMAL RECESSIVE HYPERCHOLESTEROLEMIA; EVOLOCUMAB; MUTATIONS;
D O I
10.1016/j.jacl.2018.05.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, a novel class of monoclonal antibodies, reduces low-density lipoprotein cholesterol levels and improves cardiovascular outcomes. Given the short time frame, these agents have been available for use; reports of nonresponse to the PCSK9 inhibitor therapy are scarce in literature. We describe 2 cases with substantially lesser than expected low-density lipoprotein cholesterol lowering on PCSK9 therapy. Nonresponse to PCSK9 inhibition was attributed to autosomal recessive hypercholesterolemia (secondary to low-density lipoprotein receptor adaptor protein 1 mutation) and plasmapheresis after PCSK9 inhibitor drug injections. Additional PCSK9 inhibitor nonresponders are likely to emerge as the use of these agents increases overtime. Published by Elsevier Inc. on behalf of National Lipid Association.
引用
收藏
页码:1141 / 1145
页数:5
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