Ten-year costs of cardiovascular disease in genetically verified familial hypercholesterolaemia compared with age- and sex-matched controls - Scorecard - MDSpire

Ten-year costs of cardiovascular disease in genetically verified familial hypercholesterolaemia compared with age- and sex-matched controls

  • By

  • Torbjørn Wisløff

  • Liv J Mundal

  • Jannicke Igland

  • Karianne Svendsen

  • Martin Prøven Bogsrud

  • Ivar Sønbø Kristiansen

  • Kjetil Retterstøl

  • September 23, 2025

  • 0 min

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Clinical Scorecard: A Decade of Cardiovascular Disease Expenses in Genetically Confirmed Familial Hypercholesterolaemia Compared to Age- and Sex-Matched Controls

At a Glance

CategoryDetail
ConditionFamilial hypercholesterolaemia (FH), an inherited disorder causing high LDL-cholesterol and increased cardiovascular disease risk
Key MechanismsGenetic variants in LDL receptor gene leading to elevated plasma LDL-cholesterol from birth, increasing risk of premature cardiovascular disease
Target PopulationPatients with genetically verified familial hypercholesterolaemia
Care SettingNorwegian healthcare system with tax-funded hospital and pharmaceutical care

Key Highlights

  • Patients with FH had approximately three times higher cardiovascular disease-related hospital costs than age- and sex-matched controls over 10 years.
  • Pharmaceutical costs related to cardiovascular disease were more than 10 times higher in FH patients compared to controls, with a notable increase due to PCSK9 inhibitors.
  • During 2010–2019, pharmaceutical costs increased while hospital care costs decreased in both FH and control populations.

Guideline-Based Recommendations

Diagnosis

  • Genetic testing for LDL receptor gene variants to confirm familial hypercholesterolaemia.

Management

  • Use of diet and lipid-lowering medications to reduce LDL-cholesterol and atherosclerosis risk.
  • Incorporation of proprotein convertase subtilisin/kexin Type 9 (PCSK9) inhibitors as part of pharmaceutical treatment.

Monitoring & Follow-up

  • Regular follow-up of cardiovascular disease-related hospitalizations and pharmaceutical treatments using comprehensive health registries.

Risks

  • Increased risk of premature cardiovascular disease including acute myocardial infarction, aortic stenosis, peripheral artery disease, atrial fibrillation, and heart failure.

Patient & Prescribing Data

Individuals with genetically verified familial hypercholesterolaemia in Norway

Pharmaceutical costs doubled over 10 years largely due to introduction of PCSK9 inhibitors; statins and other lipid-lowering therapies are standard.

Clinical Best Practices

  • Early genetic diagnosis of FH to enable timely intervention.
  • Comprehensive use of lipid-lowering therapies including newer agents like PCSK9 inhibitors to manage elevated LDL-cholesterol.
  • Utilization of national health registries for monitoring resource use and outcomes.
  • Consideration of cost implications in treatment planning and healthcare policy.

References

Original Source(s)

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