Plasma PCSK9 concentrations correlate with LDL and total cholesterol in diabetic patients and are decreased by fenofibrate treatment

被引:152
作者
Lambert, Gilles [1 ,2 ]
Ancellin, Nicolas
Charlton, Francesca [1 ]
Comas, Daniel [3 ]
Pilot, Julia [3 ]
Keech, Anthony [4 ]
Patel, Sanjay [1 ]
Sullivan, David R. [4 ]
Cohn, Jeffrey S. [1 ]
Rye, Kerry-Anne [1 ,5 ]
Barter, Philip J. [1 ,5 ]
机构
[1] Heart Res Inst, Sydney, NSW, Australia
[2] Univ Nantes, INSERM, U539, Nantes, France
[3] GlaxoSmithKline Inc, CVU CEDD, Les Ulis, France
[4] Royal Prince Alfred Hosp, Sydney, NSW, Australia
[5] Univ Sydney, Sydney, NSW 2006, Australia
关键词
D O I
10.1373/clinchem.2007.099747
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Proprotein convertase subtilisin/kexin type 9 (PCSK9) promotes the degradation of the LDL receptor (LDLr) in hepatocytes, and its expression in mouse liver has been shown to decrease with fenofibrate treatment. METHODS: We developed a sandwich ELISA using recombinant human PCSK9 protein and 2 affinity-purified polyclonal antibodies directed against human PCSK9. We measured circulating PCSK9 concentrations in 115 diabetic patients from the FIELD (Fenofibrate Intervention and Event Lowering in Diabetes) study before and after fenofibrate treatment. RESULTS: We found that plasma PCSK9 concentrations correlate with total (r = 0.45, P = 0.006) and LDL (r = 0.54, P = 0.001) cholesterol but not with triglycerides or HDL cholesterol concentrations in that cohort. After 6 weeks of treatment with comicronized fenofibrate (200 mg/day), plasma PCSK9 concentrations decreased by 8.5% (P = 0.041 vs pretreatment). This decrease correlated with the efficacy of fenofibrate, as judged by a parallel reduction in plasma triglycerides (r = 0.31, P = 0.015) and LDL cholesterol concentrations (r = 0.27, P = 0.048). CONCLUSIONS: We conclude that this decrease in PCSK9 explains at least in part the LDL cholesterol-lowering effects of fenofibrate. Fenofibrate might be of interest to further reduce cardiovascular risk in patients already treated with a statin. C 2008 American Association for Clinical Chemistry.
引用
收藏
页码:1038 / 1045
页数:8
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