NCT04101149

Genetic Causes of Familial Hypercholesterolemia

Genetiska Orsaker Till familjär Hyperkolesterolemi- Mekanism, Prognos Och Individanpassad Behandling

• Status: Active Not Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 150 (estimated)
• Sponsor: Region Örebro County · Academic / Other
• Sex: All
• Age: 8 Years
• Healthy volunteers: Not accepted

Summary

Familial hypercholesterolemia (FH) is a common disease. The genetic background to FH is not yet fully understood. In the present prospective cohort study we aim to study the association between different clinical characteristics, gene mutations and prognosis.

Detailed description

In this prospective observational cohort study of patients with high clinical suspicion of familial hypercholesterolemia (FH) we aim to study the association between different clinical characteristics, gene mutations and prognosis. The included patients will undergo physical examination and extended blood sampling. DNA will be extracted and used for both whole genome sequencing and investigation of both known- , unknown- and suspected mutations associated with FH. The patients will be followed in for 15 years in the Swedish patients registry and the Swedish cause of death registry.

Conditions

• Familial Hypercholesterolemia

Interventions

Type	Name	Description
OTHER	No intervention	No intervention.

Timeline

• Start date: 2019-09-01
• Primary completion: 2025-12-01
• Completion: 2045-12-01
• First posted: 2019-09-24
• Last updated: 2025-04-08

Locations

1 site across 1 country: Sweden