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Novel circulating lipid measurements for current dyslipidemias in non-treated patients undergoing coronary angiography: PCSK9 apoC3 and sdLDL-C

机译:进行冠状动脉造影的未治疗患者当前血脂异常的新型循环脂质测量:PCSK9apoC3和sdLDL-C

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摘要

Plasma levels of proprotein convertase subtilisin/kexin type 9 (PCSK9), apolipoprotein C-III (apoC3) and small dense low density lipoprotein cholesterol (sdLDL-C), have been recently recognized as circulating atherosclerosis-related lipid measurements. We aimed to elucidate their associations with current dyslipidemias, and identify their levels at increased risk to dyslipidemia. A total of 1,605 consecutive, non-treated patients undergoing diagnostic/interventional coronary angiography were examined. Plasma PCSK9 and apoC3 levels were determined using a validated ELISA assay, and sdLDL-C was measured by the Lipoprint LDL System. Plasma levels of PCSK9, apoC3, and sdLDL-C were associated with the current dyslipidemias classification (all p<0.001). PCSK9 significantly conferred prediction of both hypercholesterolemia and combined hyperlipidemia at a level of 235 ng/ml; apoC3 levels for hypertriglyceridemia, hypercholesterolemia and combined hyperlipidemia were 80.0, 71.5, and 86.4 g/ml, respectively; and sdLDL-C for hypertriglyceridemia, hypercholesterolemia, combined hyperlipidemia and hypo high density lipoprotein (HDL) cholesterolemia 3.5, 2.5, 4.5, and 2.5 mg/dl, respectively (all p<0.001 for area under the receiver-operating characteristic curve). In a polytomous logistic model comparing increasing LDL-C categories, the interactions with high PCSK9, apoC3, and sdLDL-C elevated gradually. Similarly, apoC3 and sdLDL-C showed elevated interaction with increased triglyceride categories, and only sdLDL-C showed interaction with decreased HDL cholesterol (HDL-C) categories. Furthermore, discordances of PCSK9, apoC3, and sdLDL-C with current dyslipidemias were observed. PCSK9, apoC3, and sdLDL-C showed significant interactions with current dyslipidemias, and were predictive in the screening. The substantial discordances with current dyslipidemias might provide novel view in lipid management and further cardiovascular benefit.
机译:血浆水平的前蛋白转化酶枯草杆菌蛋白酶/ kexin类型9(PCSK9),载脂蛋白C-III(apoC3)和小的致密的低密度脂蛋白胆固醇(sdLDL-C),最近已被认为是与循环动脉粥样硬化相关的脂质测定。我们旨在阐明他们与当前血脂异常的关系,并确定其血脂异常风险增加的水平。共检查了1,605例接受诊断/介入性冠状动脉造影的连续未治疗患者。使用经过验证的ELISA分析确定血浆PCSK9和apoC3的水平,并通过Lipoprint LDL系统测量sdLDL-C。血浆PCSK9,apoC3和sdLDL-C的水平与目前的血脂异常分类相关(所有p <0.001)。 PCSK9以235 ng / ml的水平显着提高了高胆固醇血症和合并高脂血症的预测;高甘油三酸酯血症,高胆固醇血症和合并高脂血症的apoC3水平分别为80.0、71.5和86.4 g / ml; sdLDL-C和sdLDL-C分别治疗高甘油三酯血症,高胆固醇血症,合并的高脂血症和高密度脂蛋白(HDL)胆固醇血症3.5、2.5、4.5和2.5 mg / dl(在接受者操作特征曲线下的面积均p <0.001)。在比较增加的LDL-C类别的多态逻辑模型中,与高PCSK9,apoC3和sdLDL-C的相互作用逐渐提高。同样,apoC3和sdLDL-C与增加的甘油三酸酯类别之间相互作用增强,只有sdLDL-C与减少的HDL胆固醇(HDL-C)类别之间相互作用。此外,观察到PCSK9,apoC3和sdLDL-C与当前血脂异常之间的不一致。 PCSK9,apoC3和sdLDL-C与目前的血脂异常显示出显着的相互作用,并且在筛查中具有预测性。与目前血脂异常的实质性矛盾可能会为脂质管理和进一步的心血管益处提供新的见解。

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