TY - JOUR
T1 - Statin treatment in children with familial hypercholesterolemia - The younger, the better
AU - Rodenburg, Jessica
AU - Vissers, Maud N.
AU - Wiegman, Albert
AU - van Trotsenburg, A. S. Paul
AU - van der Graaf, Anouk
AU - de Groot, Eric
AU - Wijburg, Frits A.
AU - Kastelein, John J. P.
AU - Hutten, Barbara A.
PY - 2007
Y1 - 2007
N2 - Background - We previously demonstrated in a randomized placebo- controlled trial that 2-year pravastatin treatment induced a significant regression of carotid intima-media thickness (IMT) in 8- to 18-year-old children with familial hypercholesterolemia. Subsequently, we continued to follow up these children to explore the relation between the age of statin initiation and carotid IMT after follow- up on statin treatment. We also examined safety aspects of statin therapy during this long-term follow-up. Methods and Results - All 214 children who initially participated in the previous placebo-controlled study were eligible for the follow- up study. After completion of the placebo-controlled study, all children continued treatment with pravastatin 20 or 40 mg, depending on their age. Blood samples were taken on a regular basis for lipids and safety parameters, and a carotid IMT measurement was performed after an average treatment period of 4.5 years. Follow-up data for 186 children were available for the statistical analyses. Multivariate analyses revealed that age at statin initiation was an independent predictor for carotid IMT after follow-up with adjustment for carotid IMT at initiation of statin treatment, sex, and duration of treatment. Early initiation of statin treatment was associated with a subsequently smaller IMT. Furthermore, no serious laboratory adverse events were reported during follow- up, and statin treatment had no untoward effects on sexual maturation. Conclusions - These data indicate that early initiation of statin treatment delays the progression of carotid IMT in adolescents and young adults. The present study shows for the first time that early initiation of statin therapy in children with familial hypercholesterolemia might be beneficial in the prevention of atherosclerosis in adolescence
AB - Background - We previously demonstrated in a randomized placebo- controlled trial that 2-year pravastatin treatment induced a significant regression of carotid intima-media thickness (IMT) in 8- to 18-year-old children with familial hypercholesterolemia. Subsequently, we continued to follow up these children to explore the relation between the age of statin initiation and carotid IMT after follow- up on statin treatment. We also examined safety aspects of statin therapy during this long-term follow-up. Methods and Results - All 214 children who initially participated in the previous placebo-controlled study were eligible for the follow- up study. After completion of the placebo-controlled study, all children continued treatment with pravastatin 20 or 40 mg, depending on their age. Blood samples were taken on a regular basis for lipids and safety parameters, and a carotid IMT measurement was performed after an average treatment period of 4.5 years. Follow-up data for 186 children were available for the statistical analyses. Multivariate analyses revealed that age at statin initiation was an independent predictor for carotid IMT after follow-up with adjustment for carotid IMT at initiation of statin treatment, sex, and duration of treatment. Early initiation of statin treatment was associated with a subsequently smaller IMT. Furthermore, no serious laboratory adverse events were reported during follow- up, and statin treatment had no untoward effects on sexual maturation. Conclusions - These data indicate that early initiation of statin treatment delays the progression of carotid IMT in adolescents and young adults. The present study shows for the first time that early initiation of statin therapy in children with familial hypercholesterolemia might be beneficial in the prevention of atherosclerosis in adolescence
U2 - https://doi.org/10.1161/CIRCULATIONAHA.106.671016
DO - https://doi.org/10.1161/CIRCULATIONAHA.106.671016
M3 - Article
C2 - 17664376
SN - 0009-7322
VL - 116
SP - 664
EP - 668
JO - Circulation
JF - Circulation
IS - 6
ER -