Evidence for improved survival with treatment of homozygous familial hypercholesterolemia.

Current Opinion in Lipidology
Alexandre M BélangerJacques Genest

Abstract

Homozygous familial hypercholesterolemia (HoFH) is an orphan disease caused by biallelic mutations at the LDL receptor (LDLR) gene, with a prevalence estimated at 1 : 250 000 to 1 : 630 000. HoFH is characterized by extremely elevated plasma levels of LDL-C greater than 10 mmol/l (>387 mg/dl), tendinous and cutaneous xanthomas in youth and premature atherosclerotic cardiovascular disease (ASCVD). The expected prevalence varies from country to country depending on the presence of founder effects, genetic probability and life expectancy. Untreated, HoFH is a fatal condition before age 30. Plasma levels of LDL-C are the major cause of mortality and the therapeutic target. Statin therapy led to a remarkable improvement in survival but is of limited use in loss-of-function LDLR gene variants or 'null' mutations. Inhibitors of PCSK9 are a useful adjunct in patients with LDLR mutations with residual activity. Extracorporeal LDL filtration has improved survival since its introduction three decades ago. Novel therapies, not dependent on a functioning LDLR include lomitapide and mipomersen, which decrease hepatic apolipoprotein B secretion, and evinacumab, directed at the angiopoietin like-3 protein (ANGPLT-3). Over the past 3-4 decades,...Continue Reading

References

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Citations

Jun 22, 2021·Biochimie·Stéphane OrlowskiEric Bruckert
Aug 26, 2021·Patterns·Shuting JinXiangxiang Zeng
Oct 23, 2021·Endocrine Reviews·Amanda J Berberich, Robert A Hegele

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