Login / Signup

Comparison between the Friedewald, Martin and Sampson Equations and LDL-C Quantification by Ultracentrifugation in a Mexican Population.

Giovanny Fuentevilla-ÁlvarezMaría Elena SotoJosé Antonio García ValdiviaYazmín Estela Torres-PazReyna SámanoIsrael Pérez-TorresRicardo GamboaClaudia Huesca-Gómez
Published in: Diagnostics (Basel, Switzerland) (2024)
Low-density lipoprotein cholesterol (LDL-C), which makes up about 70% of the cholesterol in the blood, is critical in the formation of arteriosclerotic plaques, increasing the risk of heart disease. LDL-C levels are estimated using Friedewald, Martin and Sampson equations, though they have limitations with high triglycerides. Our aim is to compare the effectiveness of these equations versus the ultracentrifugation technique in individuals with and without dyslipidemia and identify precision. There were 113 participants, 59 healthy controls and 54 dyslipidemic patients. Samples were collected after fasting. LDL-C was estimated using the Friedewald, Martin and Sampson equations. The purified LDL-C, ultracentrifugated and dialysized control group without dyslipidemia vs. patients with coronary artery disease (CAD) showed differences in age, HDL-C, triglycerides and glucose non-HDL-C ( p = 0.001 in all). There were correlations in CGWD between ultracentrifugation and Sampson R-squared (R 2 ) = 0.791. In the dyslipidemia control group, ultracentrifugation and Friedewald R 2 = 0.911. In patients with CAD, correlation between ultracentrifugation and Sampson R 2 = 0.892; Bland-Altman confirmed agreement in controls without dyslipidemia. The Martin and Sampson equations are interchangeable with ultracentrifugation. Conclusion: The role of LDL analysis using precise techniques is necessary to obtain better control of disease outcomes after the use of precise therapies and suggests verifying its importance through clinical trials.
Keyphrases
  • low density lipoprotein
  • clinical trial
  • coronary artery disease
  • randomized controlled trial
  • ejection fraction
  • blood glucose
  • pulmonary hypertension
  • insulin resistance
  • metabolic syndrome
  • adipose tissue