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Non-HDL-C/TG ratio indicates significant underestimation of calculated low-density lipoprotein cholesterol (LDL-C) better than TG level: a study on the reliability of mathematical formulas used for LDL-C estimation

  • Agnieszka Ćwiklińska ORCID logo EMAIL logo , Ewa Wieczorek , Anna Gliwińska , Marta Marcinkowska , Monika Czaplińska , Agnieszka Mickiewicz , Agnieszka Kuchta , Barbara Kortas-Stempak , Marcin Gruchała , Alicja Dębska-Ślizień , Ewa Król and Maciej Jankowski
Published/Copyright: December 24, 2020

Abstract

Objectives

Low-density lipoprotein cholesterol (LDL-C) is the main laboratory parameter used for the management of cardiovascular disease. The aim of this study was to compare measured LDL-C with LDL-C as calculated by the Friedewald, Martin/Hopkins, Vujovic, and Sampson formulas with regard to triglyceride (TG), LDL-C and non-high-density lipoprotein cholesterol (non-HDL-C)/TG ratio.

Methods

The 1,209 calculated LDL-C results were compared with LDL-C measured using ultracentrifugation-precipitation (first study) and direct (second study) methods. The Passing-Bablok regression was applied to compare the methods. The percentage difference between calculated and measured LDL-C (total error) and the number of results exceeding the total error goal of 12% were established.

Results

There was good correlation between the measurement and calculation methods (r 0.962–0.985). The median total error ranged from −2.7%/+1.4% (first/second study) for Vujovic formula to −6.7%/−4.3% for Friedewald formula. The numbers of underestimated results exceeding the total error goal of 12% were 67 (Vujovic), 134 (Martin/Hopkins), 157 (Samspon), and 239 (Friedewald). Less than 7% of those results were obtained for samples with TG >4.5 mmol/L. From 57% (Martin/Hopkins) to 81% (Vujovic) of underestimated results were obtained for samples with a non-HDL-C/TG ratio of <2.4.

Conclusions

The Martin/Hopkins, Vujovic and Sampson formulas appear to be more accurate than the Friedewald formula. To minimize the number of significantly underestimated LDL-C results, we propose the implementation of risk categories according to non-HDL-C/TG ratio and suggest that for samples with a non-HDL-C/TG ratio of <1.2, the LDL-C level should not be calculated but measured independently from TG level.


Corresponding author: Agnieszka Ćwiklińska, Department of Clinical Chemistry, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland, E-mail:

Funding source: Medical University of Gdańsk

Award Identifier / Grant number: ST 02-0125/07/524

  1. Research funding: Medical University of Gdańsk grant no. ST 02–0125/07/524.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in the first study. In the second study, retrospective data was collected anonymously from laboratory database.

  5. Ethical approval: Research involving human subjects complied with all relevant national regulations, institutional policies and is in accordance with the tenets of the Helsinki Declaration (as revised in 2013), and has been approved by the Independent Bioethics Commission for Research of the Medical University of Gdańsk (Poland) (NKBBN 541/2014-2015 and 612/2017-2018).

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2020-1366).


Received: 2020-09-08
Accepted: 2020-12-15
Published Online: 2020-12-24
Published in Print: 2021-04-27

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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