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Updated: Sep 30, 2025

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
[Cascade genetic testing of familial hypercholesterolemia A new opportunity for prevention]
Audrey Butty1, Thomas Von Känel2, Augusto Gallino3
1Consultation de prévention cardiovasculaire - cholestérol et style de vie, Département promotion de la santé et préventions, Unisanté, 1011 Lausanne.
Abstract:
Familial hypercholesterolemia (FH) is a genetic disorder associated with an increased risk of early-onset cardiovascular events. Because lifestyle interventions and lipid-lowering drugs can strongly reduce cardiovascular risk, the early diagnosis of FH is important. Indeed, given the autosomal dominant transmission of the pathogenic variant, a genetic cascade screening program of first-degree relatives from an index case could identify patients at high cardiovascular risk. In Switzerland, genetic testing for FH is rarely used, because it is not reimbursed by health insurance companies. To test the usefulness of cascade genetic testing for FH, the CATCH study is currently ongoing in all linguistic part of Switzerland.
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