Lakoski Susan G, Lagace Thomas A, Cohen Jonathan C, Horton Jay D, Hobbs Helen H
Donald W. Reynolds Cardiovascular Clinical Research Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9046, USA.
J Clin Endocrinol Metab. 2009 Jul;94(7):2537-43. doi: 10.1210/jc.2009-0141. Epub 2009 Apr 7.
PCSK9 is a secreted protein that influences plasma levels of low-density lipoprotein cholesterol (LDL-C) and susceptibility to coronary heart disease. PCSK9 is present in human plasma, but the factors that contribute to differences in plasma concentrations of PCSK9 and how they impact on the levels of lipoproteins have not been well-characterized.
The aim of the study was to measure PCSK9 levels in a large, ethnically diverse population (n = 3138) utilizing a sensitive and specific sandwich ELISA.
We conducted an observational study in the Dallas Heart Study, a multiethnic, probability-based sample of Dallas County.
Plasma levels of PCSK9 varied over approximately 100-fold range (33-2988 ng/ml; median, 487 ng/ml). Levels were significantly higher in women (517 ng/ml) than in men (450 ng/ml), and in postmenopausal women compared to premenopausal women (P < 0.0001), irrespective of estrogen status. Plasma levels of PCSK9 correlated with plasma levels of LDL-C (r = 0.24) but explained less than 8% of the variation in LDL-C levels (r(2) = 0.073). Other factors that correlated with PCSK9 levels included plasma levels of triglycerides, insulin, and glucose. Individuals with loss-of-function mutations in PCSK9 and reduced plasma levels of LDL-C also had significantly lower plasma levels of PCSK9 after adjusting for age, gender, and LDL-C levels (P < 0.0001).
Multiple metabolic and genetic factors contribute to variation in plasma levels of PCSK9 in the general population. Although levels of PCSK9 correlate with plasma levels of LDL-C, they account for only a small proportion of the variation in the levels of this lipoprotein.
前蛋白转化酶枯草溶菌素9(PCSK9)是一种分泌蛋白,可影响低密度脂蛋白胆固醇(LDL-C)的血浆水平及冠心病易感性。PCSK9存在于人体血浆中,但导致PCSK9血浆浓度差异的因素及其对脂蛋白水平的影响尚未得到充分表征。
本研究旨在使用灵敏且特异的夹心酶联免疫吸附测定法(ELISA),测量一个种族多样化的大样本群体(n = 3138)中的PCSK9水平。
我们在达拉斯心脏研究中开展了一项观察性研究,该研究是达拉斯县基于概率的多民族样本。
PCSK9的血浆水平在约100倍的范围内变化(33 - 2988纳克/毫升;中位数为487纳克/毫升)。女性(517纳克/毫升)的水平显著高于男性(450纳克/毫升),绝经后女性高于绝经前女性(P < 0.0001),与雌激素状态无关。PCSK9的血浆水平与LDL-C的血浆水平相关(r = 0.24),但仅解释了LDL-C水平变异的不到8%(r² = 0.073)。与PCSK9水平相关的其他因素包括甘油三酯、胰岛素和葡萄糖的血浆水平。在调整年龄、性别和LDL-C水平后,携带PCSK9功能丧失突变且LDL-C血浆水平降低的个体,其PCSK9的血浆水平也显著更低(P < 0.0001)。
多种代谢和遗传因素导致一般人群中PCSK9血浆水平存在差异。尽管PCSK9水平与LDL-C的血浆水平相关,但它们仅占该脂蛋白水平变异的一小部分。