Ten-year costs of cardiovascular disease in genetically verified familial hypercholesterolaemia compared with age- and sex-matched controls - Scorecard - MDSpire
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Ten-year costs of cardiovascular disease in genetically verified familial hypercholesterolaemia compared with age- and sex-matched controls
Clinical Scorecard: A Decade of Cardiovascular Disease Expenses in Genetically Confirmed Familial Hypercholesterolaemia Compared to Age- and Sex-Matched Controls
At a Glance
Category
Detail
Condition
Familial hypercholesterolaemia (FH), an inherited disorder causing high LDL-cholesterol and increased cardiovascular disease risk
Key Mechanisms
Genetic variants in LDL receptor gene leading to elevated plasma LDL-cholesterol from birth, increasing risk of premature cardiovascular disease
Target Population
Patients with genetically verified familial hypercholesterolaemia
Care Setting
Norwegian 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.