Genetics
Lp(a) drives progressive carotid wall thickening in children with familial hypercholesterolaemia followed 20 years into adulthood, a Dutch cohort of 200 (Lancet Diabetes Endocrinol 2023)
Original title: Lipoprotein(a) and carotid intima-media thickness in children with familial hypercholesterolaemia in the Netherlands: a 20-year follow-up study
In a 20-year follow-up of 214 children (aged 8-18 years) with heterozygous familial hypercholesterolaemia (FH) originally enrolled in an Amsterdam statin trial (1997-1999), 200 had at least one carotid intima-media thickness (cIMT) measurement and Lp(a) concentration recorded. Baseline median Lp(a) was 18.5 nmol/L (IQR 8.7-35.5) and mean cIMT was 0.4465 mm. Adjusted for sex, age, corrected LDL cholesterol, statin use and BMI, higher Lp(a) was significantly associated with cIMT progression over follow-up (adjusted beta 0.0073 mm per 50 nmol/L increase in Lp(a), 95% CI 0.0013-0.0132, P=0.017). The findings identify Lp(a) as an independent, additional risk factor for early atherosclerosis in children with FH, supporting routine Lp(a) measurement in this high-risk paediatric population.
Original abstract
Background: Elevated lipoprotein(a) and familial hypercholesterolaemia are both independent risk conditions for cardiovascular disease. Although signs of atherosclerosis can be observed in children with familial hypercholesterolaemia, it is unknown whether elevated lipoprotein(a) is an additional risk factor for atherosclerosis in these young patients. Therefore, we aimed to assess the contribution of lipoprotein(a) concentrations to arterial wall thickening (as measured by carotid intima-media thickness) in children with familial hypercholesterolaemia who were followed up into adulthood.
Methods: We conducted a 20-year follow-up study of 214 children (aged 8-18 years) with heterozygous familial hypercholesterolaemia who were randomly assigned in a statin trial in Amsterdam (Netherlands) between Dec 7, 1997, and Oct 4, 1999. At baseline, and at 2, 10, and 20 years thereafter, blood samples were taken and carotid intima-media thickness was measured. Linear mixed-effects models were used to evaluate the association between lipoprotein(a) and carotid intima-media thickness during follow-up. We adjusted for sex, age, corrected LDL-cholesterol, statin use, and BMI.
Findings: Our study population comprised 200 children who had a carotid intima-media thickness measurement and a measured lipoprotein(a) concentration from at least one visit available. Mean age at baseline was 13·0 years (SD 2·9), 106 (53%) children were male, and 94 (47%) were female. At baseline, median lipoprotein(a) concentration was 18·5 nmol/L (IQR 8·7-35·5) and mean carotid intima-media thickness was 0·4465 mm (SD 0·0496). During follow-up, higher lipoprotein(a) concentrations contributed significantly to progression of carotid intima-media thickness (β adjusted 0·0073 mm per 50 nmol/L increase in lipoprotein(a) [95% CI 0·0013-0·0132]; p=0·017).
Interpretation: Our findings suggest that lipoprotein(a) concentrations contribute significantly to arterial wall thickening in children with familial hypercholesterolaemia who were followed-up until adulthood, suggesting that lipoprotein(a) is an independent and additional risk factor for early atherosclerosis in those already at increased risk. Lipoprotein(a) measurement in young patients with familial hypercholesterolaemia is crucial to identify those at potentially highest risk for cardiovascular disease.
Funding: Silence Therapeutics.
childrenDutch researchfamilial hypercholesterolaemiagenetics
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.