Comparing calculated LDL-C with directly measured LDL-C in healthy and in dyslipidemic children

Anastasia Garoufi1, Antonis Drakatos2, Charalampos Tsentidis3

  • 1Second Department of Pediatrics, National and Kapodistrian University of Athens, Medical School, "P & A Kyriakou" Children's Hospital, Athens, Attica, Greece.

Clinical Biochemistry
|November 13, 2016
PubMed

Insights

Friedewald formula (FF) is more accurate for screening, while Anandaraja's formula (AF) is better for evaluating dyslipidemic children's LDL-C levels. Both formulas show high correlation but can misclassify actual LDL-C, impacting treatment decisions.

Area of Science:

  • Pediatric Endocrinology
  • Clinical Chemistry
  • Cardiovascular Disease Risk Assessment

Background:

  • Low-density lipoprotein cholesterol (LDL-C) is a key marker for atherosclerosis in children.
  • Therapeutic decisions for pediatric dyslipidemia rely on accurate LDL-C measurements.
  • Calculated LDL-C (cLDL-C) using Friedewald formula (FF) or Anandaraja's formula (AF) may deviate from directly measured LDL-C (dLDL-C).

Purpose of the Study:

  • To compare the accuracy of cLDL-C derived from FF and AF against dLDL-C in pediatric populations.
  • To evaluate the utility of these formulas in screening and managing dyslipidemic children.
  • To assess potential misclassification rates of LDL-C levels using calculated methods.

Main Methods:

  • A cohort of 1005 children aged 2-18 years was studied, divided into a general check-up group (A, n=688) and a dyslipidemic group (B, n=317).
  • Fasting serum lipid profiles were obtained.
  • LDL-C was measured directly (dLDL-C) using a homogenous assay and calculated (cLDL-C) using FF and AF.

Main Results:

  • Both FF and AF demonstrated high correlation with dLDL-C.
  • FF underestimated dLDL-C in 75.6% (group A) and 77.3% (group B), with significant mean differences in group B.
  • AF overestimated dLDL-C, showing significant mean differences in group A and leading to potential misclassification in dyslipidemic children.

Conclusions:

  • FF is a more accurate screening tool for LDL-C in children compared to AF.
  • AF is more suitable for the evaluation and follow-up of dyslipidemic children.
  • Both calculated methods carry a risk of misclassifying LDL-C levels, potentially affecting clinical management.
Abstract

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