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糖尿病患者血浆前蛋白转化酶枯草溶菌素9(PCSK9)浓度与低密度脂蛋白(LDL)及总胆固醇相关,且非诺贝特治疗可使其降低。

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

作者信息

Lambert Gilles, Ancellin Nicolas, Charlton Francesca, Comas Daniel, Pilot Julia, Keech Anthony, Patel Sanjay, Sullivan David R, Cohn Jeffrey S, Rye Kerry-Anne, Barter Philip J

机构信息

The Heart Research Institute, Sydney, Australia.

出版信息

Clin Chem. 2008 Jun;54(6):1038-45. doi: 10.1373/clinchem.2007.099747. Epub 2008 Apr 24.

Abstract

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.

摘要

背景

前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)促进肝细胞中低密度脂蛋白受体(LDLr)的降解,并且已显示其在小鼠肝脏中的表达随非诺贝特治疗而降低。

方法

我们使用重组人PCSK9蛋白和2种针对人PCSK9的亲和纯化多克隆抗体制备了一种夹心ELISA。我们在FIELD(糖尿病患者非诺贝特干预与事件降低)研究中测量了115例糖尿病患者在非诺贝特治疗前后的循环PCSK9浓度。

结果

我们发现,在该队列中,血浆PCSK9浓度与总胆固醇(r = 0.45,P = 0.006)和低密度脂蛋白胆固醇(r = 0.54,P = 0.001)相关,但与甘油三酯或高密度脂蛋白胆固醇浓度无关。在用微粒化非诺贝特(200 mg/天)治疗6周后,血浆PCSK9浓度降低了8.5%(与治疗前相比,P = 0.041)。这种降低与非诺贝特的疗效相关,这可通过血浆甘油三酯(r = 0.31,P = 0.015)和低密度脂蛋白胆固醇浓度的平行降低来判断(r = 0.27,P = 0.048)。

结论

我们得出结论,PCSK9的这种降低至少部分解释了非诺贝特降低低密度脂蛋白胆固醇的作用。非诺贝特可能对于进一步降低已经接受他汀类药物治疗的患者的心血管风险具有意义。

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