Assessment of the Prevalence of Steatotic Liver Disease Associated With Metabolic Dysfunction in Patients With Heterozygous Familial Hypercholesterolemia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age35+
SponsorNantes University Hospital

About this trial

The main goal of the STEATO-FH study is to determine the prevalence of liver steatosis within the Heterozygous Familial Hypercholesterolemia patient population.

Eligibility criteria

Qualifiers

Patient aged 35 or over

Consultation at Nantes, Rennes or Angers University Hospital during the inclusion period

With a diagnosis of familial hypercholesterolemia defined by the presence of a genetic variant, ACMG classes 4 & 5 on LDLR, APOB or PCSK9

Patient not objecting to inclusion in study (no written objection)

Disqualifiers

Protected patients: minors, adults under guardianship, curatorship and/or safeguard of justice

Pregnant or breast-feeding

Active viral hepatitis

Hemochromatosis

Trial design

Treatments tested in this trial

  • Fibroscan
  • Sample collection

Treatment groups

200 Participants
are divided into 1 treatment group

Sponsors and collaborators

Nantes University Hospital

Lead sponsor

University Hospital, Angers

Collaborator

Rennes University Hospital

Collaborator