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Is Liver Transplant Curative in Homozygous Familial Hypercholesterolemia? A Review of Nine Global Cases

  • Published:2022-04-26 Issue:6 Volume:39 Page:3042-3057
  • ISSN:0741-238X
  • Container-title:Advances in Therapy
  • language:en
  • Short-container-title:Adv Ther

Author:

Al Dubayee Mohammed,Kayikcioglu Meral,van Lennep Jeanine Roeters,Hergli Nadia,Mata Pedro

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Medicine

Reference55 articles.

1. Cuchel M, Bruckert E, Ginsberg HN, et al. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. Eur Heart J. 2014;35(32):2146–57. https://doi.org/10.1093/eurheartj/ehu274.

2. Alves AC, Alonso R, Diaz-Diaz JL, et al. Phenotypical, clinical, and molecular aspects of adults and children with homozygous familial hypercholesterolemia in Iberoamerica. Arterioscler Thromb Vasc Biol. 2020;40(10):2508–15. https://doi.org/10.1161/ATVBAHA.120.313722.

3. Wiegman A, Gidding SS, Watts GF, et al. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment. Eur Heart J. 2015. https://doi.org/10.1093/eurheartj/ehv157.

4. Landmesser U, John Chapman M, Farnier M, et al. European Society of Cardiology/European Atherosclerosis Society Task Force consensus statement on proprotein convertase subtilisin/kexin type 9 inhibitors: practical guidance for use in patients at very high cardiovascular risk. Eur Heart J. 2016. https://doi.org/10.1093/eurheartj/ehw480.

5. Cuchel M, Meagher EA, du Toit TH, et al. Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study. Lancet. 2013;381(9860):40–6. https://doi.org/10.1016/S0140-6736(12)61731-0.
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