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Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab

Patients with homozygous familial hypercholesterolemia (HoFH) have extremely elevated levels of low-density lipoprotein cholesterol (LDL-C), with premature atherosclerosis and aortic valve disease. Available drug treatments are inadequate, and even with serial apheresis, HoFH patients rarely achieve...

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Detalles Bibliográficos
Autores principales: Jeraj, Natasha, Huang, Shih-Han S., Kennedy, Brooke A., Hegele, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978082/
https://www.ncbi.nlm.nih.gov/pubmed/35386132
http://dx.doi.org/10.1016/j.cjco.2021.11.009
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author Jeraj, Natasha
Huang, Shih-Han S.
Kennedy, Brooke A.
Hegele, Robert A.
author_facet Jeraj, Natasha
Huang, Shih-Han S.
Kennedy, Brooke A.
Hegele, Robert A.
author_sort Jeraj, Natasha
collection PubMed
description Patients with homozygous familial hypercholesterolemia (HoFH) have extremely elevated levels of low-density lipoprotein cholesterol (LDL-C), with premature atherosclerosis and aortic valve disease. Available drug treatments are inadequate, and even with serial apheresis, HoFH patients rarely achieve acceptable LDL-C levels. Evinacumab is a monoclonal antibody against angiopoietin-like protein 3 that lowers LDL-C via a novel receptor-independent mechanism. We describe an Ontario patient with HoFH who for 17 months has been treated with monthly infusions of evinacumab added to pre-existing statin, ezetimibe, and evolocumab therapy. Evinacumab in this HoFH patient was associated with markedly improved LDL-C levels and decreased frequency of apheresis.
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spelling pubmed-89780822022-04-05 Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab Jeraj, Natasha Huang, Shih-Han S. Kennedy, Brooke A. Hegele, Robert A. CJC Open Case Report Patients with homozygous familial hypercholesterolemia (HoFH) have extremely elevated levels of low-density lipoprotein cholesterol (LDL-C), with premature atherosclerosis and aortic valve disease. Available drug treatments are inadequate, and even with serial apheresis, HoFH patients rarely achieve acceptable LDL-C levels. Evinacumab is a monoclonal antibody against angiopoietin-like protein 3 that lowers LDL-C via a novel receptor-independent mechanism. We describe an Ontario patient with HoFH who for 17 months has been treated with monthly infusions of evinacumab added to pre-existing statin, ezetimibe, and evolocumab therapy. Evinacumab in this HoFH patient was associated with markedly improved LDL-C levels and decreased frequency of apheresis. Elsevier 2021-11-29 /pmc/articles/PMC8978082/ /pubmed/35386132 http://dx.doi.org/10.1016/j.cjco.2021.11.009 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Jeraj, Natasha
Huang, Shih-Han S.
Kennedy, Brooke A.
Hegele, Robert A.
Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab
title Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab
title_full Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab
title_fullStr Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab
title_full_unstemmed Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab
title_short Treatment of Homozygous Familial Hypercholesterolemia With Evinacumab
title_sort treatment of homozygous familial hypercholesterolemia with evinacumab
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978082/
https://www.ncbi.nlm.nih.gov/pubmed/35386132
http://dx.doi.org/10.1016/j.cjco.2021.11.009
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