Familial hypercholesterolaemia (FH) is a common genetic disorder characterized by lifelong elevated low-density lipoprotein cholesterol (LDL-C) concentrations, which increase the risk of premature atherosclerotic cardiovascular disease (ASCVD).
FH affects around 1 in 300 people worldwide, while the more severe form, Homozygous FH (HoFH), affects about 1 in 300,000 people and can lead to serious cardiovascular complications already in childhood.
🚨 Early diagnosis and treatment can dramatically improve — and even normalize — life expectancy. Yet, fewer than 10% of affected children in Europe are currently identified.
The European Atherosclerosis Society (EAS) consensus statement on FH in children and adolescents highlights:
✔️ Improved diagnostic criteria
✔️ Earlier treatment initiation — sometimes from age 6
✔️ Lower LDL-C treatment targets
✔️ New lipid-lowering therapies
✔️ Updated treatment algorithms
✔️ Better transition from paediatric to adult care
The statement emphasizes one key message: reducing lifelong exposure to high LDL-C is critical to protecting cardiovascular health from an early age.
Read the full publication:
eas.to/consensus-fhinchildre…
To the press release:
eas.to/consensus-fhinchildre…
To the key messages:
eas-society.org/publications…