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Published on: September 15, 2018
Expression of common familial dyslipidemias in early childhood
J Lapinleimu1, H Lapinleimu, I O Nuotio
1Department of Medicine, University of Turku, Turku, Finland. Jouni.Lapinleimu@tyks.fi
Insights
Early identification of familial dyslipidemia in children is key to preventing heart disease. Repeatedly high non-HDL cholesterol in children of parents with high cholesterol strongly predicts their own dyslipidemia.
Area of Science:
- Cardiovascular Health
- Pediatric Lipidology
- Preventive Cardiology
Background:
- Familial dyslipidemias can lead to premature atherosclerotic disease.
- Early detection in childhood is crucial for intervention.
- Parental dyslipidemia is a significant risk factor for children.
Purpose of the Study:
- To evaluate the diagnostic value of early childhood lipid samples in identifying familial dyslipidemias.
- To assess the predictive power of deviant lipid levels in children based on parental dyslipidemia status.
Main Methods:
- Analysis of lipid data from 353 children and their parents over the first 7 years of life.
- Defined hypo-high-density-lipoprotein-cholesterol (hypo-HDL-C) and hyper-non-high-density-lipoprotein-cholesterol (hyper-non-HDL-C) based on parental and child lipid levels.
- Estimated diagnostic values using longitudinal means, quintiles, standard deviation models, and bootstrap confidence intervals.
Main Results:
- 16.7% of all children had hyper-non-HDL-C; 31.8% of children with hyper-non-HDL-C parents had this condition (p=0.008).
- A single early non-HDL-C sample in the highest quintile predicted 83% of hyper-non-HDL-C children from affected parents.
- A mean of three samples improved prediction to 91% for children with hyper-non-HDL-C parents.
Conclusions:
- Repeatedly elevated non-HDL cholesterol in children of hypercholesterolemic parents is a strong predictor of true dyslipidemia.
- Early and repeated lipid profiling in at-risk children can aid in timely diagnosis and prevention of atherosclerotic disease.
Abstract:
Early identification of common familial dyslipidemias may prevent premature atherosclerotic disease. This study estimated the diagnostic values of few early childhood repeatedly deviant lipid samples by the knowledge of the parent's dyslipidemia. The first 7 years of age data of 353 children with their parents were evaluated from atherosclerosis risk-factor intervention study controls. Parents' low high-density-lipoprotein-cholesterol concentration (hypo-HDL-C), and high total cholesterol concentration-HDL-C (hyper-non-HDL-C) were defined. True hypo-HDL-C and hyper-non-HDL-C children were defined when their respective individual longitudinal means were beyond the appropriate lipid quintiles. Sensitivities, specificities, positive and negative predictive values of the early lipid samples were estimated with individual standard deviation models and bootstrap confidence. Hypo-HDL-C children proportions were 15.3% of all, and 20.9% of the children from the hypo-HDL-C parents (p=0.26). Hyper-non-HDL-C children were 16.7% of all and 31.8% of the children from the hyper-non-HDL-C parents (p=0.008). One early non-HDL-C sample in the highest quintile predicted 56% of the hyper-non-HDL-C children from healthy parents, but 83% of the hyper-non-HDL-C children from the hyper-non-HDL-C parents. Mean of three samples improved the latter prediction to 91%. This showed that if hypercholesterolemic parent's child expressed repeatedly hyper-non-HDL-C, it predicts true dyslipidemia of the child.
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