Evinacumab for the treatment of homozygous familial hypercholesterolaemia: first patient case report in Switzerland

We present the first case in Switzerland of a patient with homozygous familial hypercholesterolaemia treated with evinacumab, a new recombinant human monoclonal antibody currently approved in Europe and in the USA but not yet in Switzerland. Homozygous familial hypercholesterolaemia is a rare genetic disorder that causes severely elevated levels of low-density lipoprotein (LDL) cholesterol and early atherosclerotic cardiovascular disease, which, if left untreated, can lead to premature death. As a result of this newly introduced treatment, the patient's LDL cholesterol levels were reduced by more than half, achieving recommended target values of secondary prevention for the first time. This case underscores the efficacy of evinacumab in achieving LDL cholesterol targets in homozygous familial hypercholesterolaemia patients and highlights the importance of early identification and treatment initiation.

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Publication Details

Journal
Swiss Medical Weekly
Published
2025-02-28
DOI
https://doi.org/10.57187/s.4024
Citations
1
Primary Topic
Lipoproteins and Cardiovascular Health
Type
article
Field-Weighted Citation Impact
2.01
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article

Evinacumab for the treatment of homozygous familial hypercholesterolaemia: first patient case report in Switzerland

Cathérine Gebhard, Noé Corpataux, Fabienne Aregger, Konstantinos C. Koskinas
1 citations
Swiss Medical Weekly
Lipoproteins and Cardiovascular Health
2.01
article

Evinacumab for the treatment of homozygous familial hypercholesterolaemia: first patient case report in Switzerland

Cathérine Gebhard, Noé Corpataux, Fabienne Aregger, Konstantinos C. Koskinas
article en
1 citations

Abstract

We present the first case in Switzerland of a patient with homozygous familial hypercholesterolaemia treated with evinacumab, a new recombinant human monoclonal antibody currently approved in Europe and in the USA but not yet in Switzerland. Homozygous familial hypercholesterolaemia is a rare genetic disorder that causes severely elevated levels of low-density lipoprotein (LDL) cholesterol and early atherosclerotic cardiovascular disease, which, if left untreated, can lead to premature death. As a result of this newly introduced treatment, the patient's LDL cholesterol levels were reduced by more than half, achieving recommended target values of secondary prevention for the first time. This case underscores the efficacy of evinacumab in achieving LDL cholesterol targets in homozygous familial hypercholesterolaemia patients and highlights the importance of early identification and treatment initiation.

Swiss Medical WeeklyVol. 155(2)
University of Bern (CH), University Hospital of Bern (CH)
Good health and well-being
Openalex Percentile: Top 18%
Lipoproteins and Cardiovascular Health
2.01
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Evinacumab for the treatment of homozygous familial hypercholesterolaemia: first patient case report in Switzerland — Cathérine Gebhard, Noé Corpataux, et al. · Swiss Medical Weekly (2025) | TGRS Research Map | TGRS