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Updated: Jan 10, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Toward accurate LDL-cholesterol estimation: platform-specific, population-based equations outperform Friedewald in
Imola Györfi1, Ion Bogdan Mănescu2,3, Oana Roxana Oprea2,3
1Doctoral School (I.O.S.U.D), George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, Romania.
None:
Low-density lipoprotein cholesterol (LDL-C) remains a key biomarker for cardiovascular risk assessment. While the Friedewald equation is widely used for estimating LDL-C, its accuracy can vary across populations and analytical platforms. This study aimed to develop and validate population-specific, platform-adapted LDL-C equations in two independent cohorts and to compare their performance with the Friedewald equation. A retrospective analysis was conducted using lipid profiles from 31,265 individuals across two datasets: a tertiary hospital (n = 10,174; Roche Cobas platform) and a private laboratory (n = 21,091; Abbott Alinity platform). For each, two linear regression models (50:50 and 80:20 random training-validation splits) were used to develop LDL-C estimation equations using total cholesterol, high-density lipoprotein cholesterol, and triglycerides as predictors. Performance was evaluated by median absolute error (MAE), median percentage error (MPE), and agreement with direct LDL-C in clinical risk categories. The training/validation models performed nearly identically; therefore, only the 50:50 models were retained for the final analysis, with one equation generated for each platform. Both novel equations showed significantly lower MAE (-0.015 to -0.010 mmol/L) and MPE (-0.5% to -0.4%) compared to the Friedewald equation (-0.217 and -0.209 mmol/L MAE; -7.4% and -6.6% MPE) and had more balanced error distributions. The Roche Cobas-derived equation achieved higher overall classification accuracy (85.1%) than the Abbott Alinity-based model (78.6%), while both substantially outperformed Friedewald (67.1% and 65.3%) in all but the <1.03 mmol/L LDL-C category. Platform-specific, population-adapted LDL-C equations offer superior accuracy and risk classification over Friedewald. These findings further support the clinical relevance of implementing such equations; however, broader validation and formal guidance from professional bodies are needed to facilitate their integration into clinical practice.
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