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Determining a new formula for calculating low-density lipoprotein cholesterol: data mining approach

机译:确定计算低密度脂蛋白胆固醇的新公式:数据挖掘方法

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摘要

Low-density lipoprotein cholesterol (LDL-C) is a risk factor of coronary heart diseases. The estimation of LDL-C (LDL-Cal) level was performed using Friedewald's equation for triglyceride (TG) level less than 400 mg/dL. Therefore, the aim of this study is to generate a new formula for LDL-Cal and validate the correlation coefficient between LDL-Cal and LDL-C directly measured (LDL-Direct). A data set of 1786 individuals receiving annual medical check-ups from the Faculty of Medical Technology, Mahidol University, Thailand in 2008 was used in this study. Lipid profiles including total cholesterol (TC), TG, high-density lipoprotein cholesterol (HDL-C) and LDL-C were determined using Roche/Hitachi modular system analyzer. The estimated LDL-C was obtained using Friedewald's equation and the homogenous enzymatic method. The level of TG was divided into 6 groups (TG<200, <300, <400, <500, <600 and < 1000 mg/dL) for constructing the LDL-Cal formula. The pace regression model was used to construct the candidate formula for the LDL-Cal and determine the correlation coefficient (r) with the LDL-Direct. The candidate LDL-Cal formula was generated for 6 groups of TG levels that displayed well correlation between LDL-Cal and LDL-Direct. Interestingly, The TG level was less than 1000 mg/dL, the regression model was able to generate the equation as shown as strong r of 0.9769 with LDL-Direct. Furthermore, external data set (n = 666) with TG measurement (36-1480 mg/dL) was used to validate new formula which displayed high r of 0.971 between LDL-Cal and LDL-direct. This study explored a new formula for LDL-Cal which exhibited higher r of 0.9769 and far beyond the limitation of TG more than 1000 mg/dL and potential used for estimating LDL-C in routine clinical laboratories.
机译:低密度脂蛋白胆固醇(LDL-C)是冠心病的危险因素。使用低于400 mg / dL的甘油三酸酯(TG)水平的Friedewald方程估算LDL-C(LDL-Cal)水平。因此,本研究的目的是为LDL-Cal生成一个新公式,并验证LDL-Cal与直接测量的LDL-C之间的相关系数(LDL-Direct)。本研究使用了2008年从泰国马西多尔大学医学技术学院接受年度体检的1786人的数据集。使用Roche / Hitachi模块化系统分析仪确定脂质谱,包括总胆固醇(TC),TG,高密度脂蛋白胆固醇(HDL-C)和LDL-C。使用弗里德瓦尔德方程和均相酶法获得估计的LDL-C。 TG的水平分为6组(TG <200,<300,<400,<500,<600和<1000 mg / dL),用于构建LDL-Cal配方。使用步伐回归模型构建LDL-Cal的候选公式,并确定与LDL-Direct的相关系数(r)。为6组TG水平生成了候选LDL-Cal公式,显示了LDL-Cal和LDL-Direct之间的良好相关性。有趣的是,TG水平小于1000 mg / dL,回归模型能够生成方程,如图所示,LDL-Direct的强r为0.9769。此外,使用外部数据集(n = 666)和TG测量(36-1480 mg / dL)来验证新公式,该公式显示LDL-Cal和LDL-direct之间的高r为0.971。这项研究探索了一种新的LDL-Cal公式,该公式表现出更高的r值为0.9769,远远超出了TG的限制,即超过1000 mg / dL,并且具有在常规临床实验室中用于评估LDL-C的潜力。

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