An improved method for estimating low LDL-C based on the enhanced Sampson-NIH equation

The accurate measurement of Low-density lipoprotein cholesterol (LDL-C) is critical in the decision to utilize the new lipid-lowering therapies like PCSK9-inhibitors (PCSK9i) for high-risk cardiovascular disease patients that do not achieve sufficiently low LDL-C on statin therapy. To improve the es...

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Veröffentlicht in:Lipids in health and disease 2024-02, Vol.23 (1), p.43-43, Article 43
Hauptverfasser: Coverdell, Tatiana C, Sampson, Maureen, Zubirán, Rafael, Wolska, Anna, Donato, Leslie J, Meeusen, Jeff W, Jaffe, Allan S, Remaley, Alan T
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Sprache:eng
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Zusammenfassung:The accurate measurement of Low-density lipoprotein cholesterol (LDL-C) is critical in the decision to utilize the new lipid-lowering therapies like PCSK9-inhibitors (PCSK9i) for high-risk cardiovascular disease patients that do not achieve sufficiently low LDL-C on statin therapy. To improve the estimation of low LDL-C by developing a new equation that includes apolipoprotein B (apoB) as an independent variable, along with the standard lipid panel test results. Using β-quantification (BQ) as the reference method, which was performed on a large dyslipidemic population (N = 24,406), the following enhanced Sampson-NIH equation (eS LDL-C) was developed by least-square regression analysis: [Formula: see text] RESULTS: The eS LDL-C equation was the most accurate equation for a broad range of LDL-C values based on regression related parameters and the mean absolute difference (mg/dL) from the BQ reference method (eS LDL-C: 4.51, Sampson-NIH equation [S LDL-C]: 6.07; extended Martin equation [eM LDL-C]: 6.64; Friedewald equation [F LDL-C]: 8.3). It also had the best area-under-the-curve accuracy score by Regression Error Characteristic plots for LDL-C 
ISSN:1476-511X
1476-511X
DOI:10.1186/s12944-024-02018-y