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• W2922307380 endingPage "717" @default.
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• W2922307380 abstract "Familial hypercholesterolaemia (FH) is a devastating genetic disease that leads to extremely high cholesterol levels and severe cardiovascular disease, mainly caused by mutations in any of the main genes involved in low-density lipoprotein cholesterol (LDL-C) uptake. Among these genes, mutations in the LDL receptor ( LDLR ) are responsible for 80%–90% of the FH cases. The severe homozygous variety (HoFH) is not successfully treated with standard cholesterol-lowering therapies, and more aggressive strategies must be considered to mitigate the effects of this disease, such as weekly/biweekly LDL apheresis. However, development of new therapeutic approaches is needed to cure HoFH. Because HoFH is mainly due to mutations in the LDLR , this disease has been proposed as an ideal candidate for gene therapy. Several preclinical studies have proposed that the transference of functional copies of the LDLR gene reduces circulating LDL-C levels in several models of HoFH, which has led to the first clinical trials in humans. Additionally, the recent development of clustered regularly interspaced short palindromic repeat/CRISPR-associated 9 technology for genome editing has opened the door to therapies aimed at directly correcting the specific mutation in the endogenous LDLR gene. In this article, we review the genetic basis of the FH disease, paying special attention to the severe HoFH as well as the challenges in its diagnosis and clinical management. Additionally, we discuss the current therapies for this disease and the new emerging advances in gene therapy to target a definitive cure for this disease." @default.
• W2922307380 created "2019-03-22" @default.
• W2922307380 creator A5040190129 @default.
• W2922307380 creator A5057374991 @default.
• W2922307380 date "2019-03-15" @default.
• W2922307380 modified "2023-10-14" @default.
• W2922307380 title "Review of the scientific evolution of gene therapy for the treatment of homozygous familial hypercholesterolaemia: past, present and future perspectives" @default.
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• W2922307380 doi "https://doi.org/10.1136/jmedgenet-2018-105713" @default.
• W2922307380 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30877235" @default.
• W2922307380 hasPublicationYear "2019" @default.
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