Direct LDL-C estimation in preschoolers: Practicable first step for FH screening
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Updated: Aug 8, 2025

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Olga Kordonouri1, Stefan Arens1, Karin Lange2
1Children's Hospital AUF DER BULT, Hannover, Germany.
Insights
Directly measuring LDL-C in preschoolers is a practical and reliable method for screening Familial Hypercholesterolemia (FH). This approach can identify children at risk for cardiovascular disease early on.
Area of Science:
- Pediatrics
- Cardiology
- Genetics
Background:
- Familial Hypercholesterolemia (FH) leads to premature cardiovascular disease due to elevated LDL-C.
- Current FH screening methods are not well-established.
Purpose of the Study:
- To assess the feasibility of screening for FH by directly measuring LDL-C levels in preschoolers.
- To evaluate the practicability of LDL-C measurement in young children for FH screening.
Main Methods:
- LDL-C was measured via capillary blood sampling in children aged 2-6 years during routine check-ups.
- Family history of dyslipidemia and/or premature cardiovascular disease was also collected.
Main Results:
- 15,009 children participated; 40.9% had a positive family history of hyperlipidemia.
- Children with a positive family history showed significantly higher LDL-C levels.
- Higher LDL-C levels (above 135 mg/dL and 160 mg/dL) were more frequent in children with a positive family history.
Conclusions:
- Direct LDL-C measurement in children aged 2-6 years is practicable and provides reliable data for FH screening.
- This method can be integrated into routine pediatric visits for effective FH screening in the general population.
Background:
Individuals with FH develop cardiovascular disease due to lifelong cumulative exposure to elevated LDL-C. Effective screening for FH is not yet established.
Objective:
To evaluate the practicability of a FH screening by measuring directly the LDL-C in preschoolers.
Methods:
LDL-C measurement through capillary blood sampling during the compulsory routine check-ups by the pediatrician in children aged 2 to 6 years including information on family history as dyslipidemia and/or premature cardiovascular disease in first and second grade of pedigrees.
Results:
15,009 children (52.2% males, median age 3.9 years [IQR 3.0-5.1]) participated in the study. Positive family history for hyperlipidemia was stated in 40.9% cases, in 12.0% also in at least one 1st degree relative. In the total cohort, median LDL-C was 93 mg/dL [IQR 79-109 mg/dL]. Boys had significantly higher LDL-C levels than girls (p < 0.0001), whereas there was no difference regarding their age (p = 0.757). Children from families with a positive history for hypercholesterolemia/dyslipidemia had significantly higher LDL-C levels (p < 0.001) and were more frequently among those with LDL-C values above 135 mg/dL (3.5 mmol/L, 96th percentile; 53.2% vs. 40.3%, p < 0.001) and those with LDL-C levels above 160 mg/dL (4.1 mmol/L, 99th percentile; 45.3% vs. 40.7%, p < 0.001) than children without positive family history.
Conclusions:
Direct measurement of LDL-C levels in children at ages 2-6 years during the compulsory routine check-ups as well as at any voluntary visits to the pediatrician's office is practicable and delivers reliable information, which can be used for a FH screening strategy in the general population.
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