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The relationship between infant and parent Lp(a) levels
D E Wilcken1, X L Wang, N P Dudman
1Department of Cardiovascular Medicine, Prince Henry Hospital, Sydney, NSW, Australia.
Chemistry and Physics of Lipids
|January 1, 1994
Summary
Apolipoprotein(a) (apo(a)) gene expression begins early, with infant levels correlating strongly with parental lipoprotein(a) (Lp(a)) by 8.5 months. Early screening can identify families at high cardiovascular risk.
Area of Science:
- Cardiovascular Science
- Genetics
- Pediatric Endocrinology
Background:
- Atherogenesis, the development of arterial plaques, can start in childhood.
- Elevated serum lipoprotein(a) (Lp(a)) levels are a known risk factor for cardiovascular disease.
- Understanding early apolipoprotein(a) (apo(a)) gene expression is crucial for early risk assessment.
Purpose of the Study:
- To investigate the early expression of the apolipoprotein(a) (apo(a)) gene in newborns.
- To examine the relationship between infant and parental serum lipoprotein(a) (Lp(a)) levels.
- To assess the predictive value of early Lp(a) measurements for identifying cardiovascular risk in families.
Main Methods:
- Analysis of apolipoprotein(a) (apo(a)) levels in 1032 newborns (3-5 days old).
- Re-measurement of Lp(a) concentrations in 51 infants at 8.5 months, along with parental samples.
- Statistical correlation and regression analyses to determine relationships between infant and parental Lp(a) levels.
Main Results:
- Infant apo(a) levels at 3-5 days showed a skewed distribution, similar to adults but lower.
- Infant Lp(a) levels at 8.5 months were highly correlated with levels at 3-5 days (r=0.73) and increased twofold.
- Infant Lp(a) levels at 8.5 months closely mirrored parental levels, with strong predictive values for parental Lp(a) >300 mg/l.
Conclusions:
- The apo(a) gene is nearly fully expressed within the first year of life.
- Infant Lp(a) levels track closely and predict parental values, indicating early genetic influence.
- Childhood Lp(a) screening can identify families with heightened cardiovascular risk for targeted prevention strategies.