Comparison of Sampson and extended Martin/Hopkins methods of low-density lipoprotein cholesterol calculations with direct measurement in pediatric patients with hypertriglyceridemia.

LDL-C calculation LDL-C direct measurement cardiovascular diseases hypertriglyceridemia low-density lipoprotein cholesterol pediatric patients

Journal

Laboratory medicine
ISSN: 1943-7730
Titre abrégé: Lab Med
Pays: England
ID NLM: 0250641

Informations de publication

Date de publication:
30 May 2023
Historique:
medline: 30 5 2023
pubmed: 30 5 2023
entrez: 30 5 2023
Statut: aheadofprint

Résumé

The Friedewald equation is the commonly used method of low-density lipoprotein cholesterol (LDL-C) calculation, requiring reflex to direct LDL-C measurement when triglycerides (TG) ≥ 400 mg/dL. Recently formulated Sampson and extended Martin/Hopkins methods have been validated with TG up to 800 mg/dL and thus have the potential to replace direct LDL-C measurement. Given the growing prevalence of childhood dyslipidemia, the objective of this study was to compare Sampson and extended Martin/Hopkins methods of LDL-C calculation with the direct measurement in a pediatric cohort with 400 ≤ TG ≤ 799 mg/dL. This study retrieved standard lipid panels and corresponding direct LDL-C measurements of 131 patients with 400 ≤ TG ≤ 799 mg/dL from a pediatric population. Following the application of Sampson and extended Martin/Hopkins calculations, calculated values were compared with direct LDL-C measurements using ordinary least squares linear regression analysis and bias plotting. Both Sampson and extended Martin/Hopkins LDL-C calculations exhibited a strong correlation with the direct measurements (Pearson r = 0.89) in patients with 400 ≤ TG ≤ 800 mg/dL. Average percentages of bias of 45% and 21% were found between the direct LDL-C measurements and Sampson or extended Martin/Hopkins calculations, respectively. Both Sampson and extended Martin/Hopkins calculations are applicable as clinical alternatives of direct LDL-C measurement in pediatric patients given 400 ≤ TG ≤ 799 mg/dL.

Identifiants

pubmed: 37253142
pii: 7186698
doi: 10.1093/labmed/lmad047
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of American Society for Clinical Pathology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

S M Touhidul Islam (SMT)

University of Texas Southwestern Medical Center, Dallas, TX, US.

Alagar R Muthukumar (AR)

University of Texas Southwestern Medical Center, Dallas, TX, US.

Patricia Mary Jones (PM)

University of Texas Southwestern Medical Center, Dallas, TX, US.
Children's Health Dallas, TX, US.

Ibrahim Hashim (I)

University of Texas Southwestern Medical Center, Dallas, TX, US.

Jing Cao (J)

University of Texas Southwestern Medical Center, Dallas, TX, US.
Children's Health Dallas, TX, US.

Classifications MeSH