Validation of a Proposed Novel Equation for Estimating LDL Cholesterol

被引:62
作者
Meeusen, Jeffrey W. [1 ]
Lueke, Alan J. [1 ]
Jaffe, Allan S. [1 ,2 ]
Saenger, Amy K. [1 ]
机构
[1] Mayo Clin, Dept Lab Med & Pathol, Div Clin Core Lab Serv, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Med, Div Cardiovasc Dis, Rochester, MN 55905 USA
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; PLASMA;
D O I
10.1373/clinchem.2014.227710
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Aggressive LDL cholesterol (LDL-C)-lowering strategies are recommended for primary and secondary prevention of cardiovascular events. A newly derived equation for LDL-C estimation was recently published that addressed limitations in the commonly used Friedewald LDL-C calculation method. The novel method was reported to classify patients with superior concordance to measured LDL-C compared to the Friedewald method, particularly in patients with LDL-C <70 mg/dL. METHODS: We evaluated the performance of the novel method within an independent cohort of 23055 patients with LDL-C measured by the gold standard beta-quantification reference method. RESULTS: Overall Friedewald underestimated and the novel method overestimated measured LDL-C. Both estimations significantly deviated from the reference method when LDL-C was <70 mg/dL. Overall, the Friedewald and novel calculations correctly classified 77% and 78% of patients, respectively. The largest discrepancy in classification was observed in individuals with measured LDL-C <70 mg/dL. For this group the novel calculation would reclassify 8.7% of patients as >70 mg/dL compared to the Friedewald equation. CONCLUSIONS: We compared both novel and Friedewald estimated LDL-C against the LDL-C reference method; in contrast, the prior study relied on validation of a subset of samples by beta-quantification to allow the use of the vertical autoprofile method for LDL-C measurement. We conclude that the novel method has some benefits but it is unclear whether improvements over the Friedewald calculation are substantive enough to justify making the change in routine clinical practice and to improve patient outcomes. (C) 2014 American Association for Clinical Chemistry
引用
收藏
页码:1519 / 1523
页数:5
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