Key result
Adolescent FH reveals CAD and subclinical atherosclerosis, highlighting challenges in LDL-C control.
Why the study?
Inadequate LDL cholesterol control drives accelerated atherosclerosis in pediatric familial hypercholesterolemia, and coronary artery disease in adolescents poses unique management challenges due to limited representation in clinical trials.
Highlights the unique management challenges and demonstrates the use of aggressive lipid-lowering therapies like plasma exchange and interventional revascularization in adolescents with severe familial hypercholesterolemia.
Familial hypercholesterolemia is primarily a disorder of reduced low-density lipoprotein (LDL) clearance, which can be inherited in either homozygous or heterozygous form. Despite the availability of various modalities to achieve target LDL cholesterol levels, inadequate control remains a significant risk factor for accelerated atherosclerosis in the pediatric population. Moreover, the occurrence of coronary artery disease in adolescents poses unique management challenges given the limited representation of this age group in clinical trials. We report 2 cases of coronary artery disease and 1 case of subclinical atherosclerosis in adolescent patients with genetically confirmed familial hypercholesterolemia, outlining the diagnostic work-up, challenges in achieving LDL cholesterol control, measures undertaken, including plasma exchange, and revascularization strategies using drug-eluting stents or drug-coated balloons, in accordance with current guidelines.
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Mishra et al. (2026) studied this question. Coronary artery disease and subclinical atherosclerosis were identified in adolescent patients with familial hypercholesterolemia, highlighting challenges in LDL cholesterol control.
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