Atabi Fereshteh, Mohammadi Reza
Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Department of Biochemistry, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Iran J Pathol. 2020 Fall;15(4):261-267. doi: 10.30699/ijp.2020.110379.2174. Epub 2020 Jul 18.
BACKGROUND & OBJECTIVE: Concentration of low-density lipoprotein (LDL) is a known risk factor for cardiovascular disease which is routinely measured or calculated as LDL-C in clinical laboratories. In order to decrease the cost, instead of its measuring, it is recommended to calculate it using multiple formulas that have been introduced up to now. The aim of this study was to assess the results of various formulas and comparison of these results with those of measuring method and to clarify the best formula for the Iranian population.
Concentrations of total cholesterol (TC), triglyceride (TG), cholesterol of high-density lipoprotein (HDL-C) and LDL-C in serums of 471 overnight fasting individuals were measured and also LDL-Cs of these samples were calculated by eleven different formulas according to their TC, TG, and HDL-C concentrations. Subsequently, results of measured and calculated LDL-C were analyzed statistically by paired t-test, correlation coefficient, and Passing-Bablok regression. In addition, for clinical evaluation, the differences between calculated and measured mean results were calculated and compared with an allowable total error.
Paired t-test unraveled a significant difference between the results of measured and calculated LDL-C by various formulas. But for some formulas, these differences were not clinically significant. The best clinical and statistical agreement (correlation coefficient) was obtained by the Friedewald equation.
By using validated methods which have correct calibration and control system for measuring TC, TG, and HDL-C, we can use the Friedewald formula for calculating LDL-C in serum samples with TG up to 400 mg/dL.
低密度脂蛋白(LDL)浓度是心血管疾病的已知危险因素,临床实验室通常将其作为LDL-C进行常规测量或计算。为了降低成本,建议不进行测量,而是使用目前已推出的多个公式来计算。本研究的目的是评估各种公式的结果,并将这些结果与测量方法的结果进行比较,以明确适用于伊朗人群的最佳公式。
测量了471名过夜禁食个体血清中的总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)和LDL-C浓度,并根据这些样本的TC、TG和HDL-C浓度,用11种不同公式计算了这些样本的LDL-C。随后,通过配对t检验、相关系数和Passing-Bablok回归对测量和计算的LDL-C结果进行统计学分析。此外,为了进行临床评估,计算了计算结果与测量平均结果之间的差异,并与允许的总误差进行比较。
配对t检验揭示了各种公式计算的LDL-C结果与测量结果之间存在显著差异。但对于某些公式,这些差异在临床上并不显著。Friedewald方程获得了最佳的临床和统计一致性(相关系数)。
通过使用具有正确校准和控制系统来测量TC、TG和HDL-C的经过验证的方法,我们可以使用Friedewald公式来计算TG高达400mg/dL的血清样本中的LDL-C。