Elevated Lp(a) with a small apo(a) isoform in children: risk factor for the development of premature coronary artery
Albert Dirisamer1, Harald Widhalm, Elsie Aldover-Macasaet
1Department of Obesity and Lipid Disorder, University of Vienna, Austria.
Insights
Elevated small-isoform Lipoprotein(a) (Lp(a)) is a significant risk factor for early cardiovascular disease in children with hypercholesterolemia. This finding highlights the importance of assessing apo(a) size and Lp(a) levels in pediatric cardiovascular risk assessment.
Area of Science:
- Cardiovascular Science
- Genetics
- Pediatric Endocrinology
Background:
- Lipoprotein(a) (Lp(a)) and apolipoprotein(a) (apo(a)) isoforms are linked to cardiovascular disease.
- Specific apo(a) isoforms combined with high Lp(a) may predict premature coronary artery disease.
Purpose of the Study:
- Investigate the association between familial history of premature coronary artery disease, apo(a) size, and Lp(a) levels in hypercholesterolemic children and adolescents.
- Utilize a novel method for determining apo(a) isoforms.
Main Methods:
- Classified apo(a) isoforms into six phenotype patterns (S1-S4, B, F) based on K-IV repeats.
- Grouped apo(a) isoforms into low-molecular-weight and high-molecular-weight categories.
- Quantified Lp(a) contribution in double-banded isoforms based on band intensity.
Main Results:
- 46% of the risk group had elevated Lp(a) with a small apo(a) isoform, compared to 20% in the control group (p < 0.05).
- Children and adolescents in the risk group showed a statistically significant higher prevalence of elevated Lp(a) levels (p < 0.05).
Conclusions:
- Elevated levels of small-isoform Lp(a) may serve as a strong, independent risk factor for premature coronary artery disease.
- This is particularly relevant in pediatric populations with hypercholesterolemia.
Background:
levels of Lp(a) and low-molecular-weight apolipoprotein(a) isoform are strongly associated with the development of early cardiovascular disease. Certain types of apo(a) isoforms in combination with elevated levels of Lp(a) may be important in the determining of premature coronary artery disease. Therefore, we investigated the association of familial history of premature coronary artery disease and apo(a) size and Lp(a) levels in children and adolescents with hypercholesterolemia using a novel method determining apo(a) isoforms.
Methods And Results:
Isoforms were classified in six phenotype patterns: S1-S4, B, F and according to their K-IV repeats. Apo(a) isoforms were divided into two groups: low-molecular- and high-molecular apo(a) isoforms. In subjects with double-banded apo(a) isoforms containing a small- and a large-isoform Lp(a) each contribution was based on the intensity of staining of the two bands. The percentage of patients with elevated levels of Lp(a) and a small apo(a) isoform (i.e. elevated small-isoform Lp(a)) was 46% in the risk group and 20% in the control group, p < 0.05. The percentage number of children and adolescents with elevated Lp(a) levels was higher in the risk group, reaching statistical significance (p < 0.05).
Conclusion:
Elevated levels of small-isoform Lp(a) might be a strong and independent risk factor for the development of premature coronary artery disease in children and adolescents with hypercholesterolemia.
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