Literature DB >> 28595549

APOC-III Antisense Oligonucleotides: A New Option for the Treatment of Hypertriglyceridemia.

Joel Schmitz1, Ioanna Gouni-Berthold1.   

Abstract

Elevated triglyceride levels (higher than ~1000 mg/dL) are associated with an increased risk for pancreatitis. Apolipoprotein-CIII (apoC-III) plays a key role in the metabolism of triglycerides and triglyceride-rich lipoproteins. Loss of function mutations in the gene encoding apoC-III (APOC3) is associated with low triglyceride levels and a decreased risk for cardiovascular disease (CVD) while overexpression of APOC3 is associated with hypertriglyceridemia. Although many drugs such as fibrates, statins and omega-3 fatty acids modestly decrease triglyceride levels (and apoC-III concentrations), there are many patients who still have severe hypertriglyceridemia and are at increased risk for pancreatitis and potentially for CVD. The antisense oligonucleotide (ASO) against APOC3 mRNA volanesorsen (previously called ISIS 304801, ISIS-ApoCIIIRx and IONIS-ApoCIIIRx) robustly decreases both, apoC-III production and triglyceride concentrations and is being currently evaluated in phase 3 trials. In this narrative review, we present the currently available clinical evidence on the efficacy and safety of volanesorsen for the treatment of hypertriglyceridemia. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

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Keywords:  Antisense oligonucleotides; IONIS-ApoCIIIRx; ISISzzm321990304801; ISIS-ApoCIIIRx; apolipoprotein C-III; hypertriglyceridemia; triglycerides; volanesorsen.

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Year:  2018        PMID: 28595549     DOI: 10.2174/0929867324666170609081612

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  4 in total

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3.  Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation.

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Review 4.  New insights into ANGPLT3 in controlling lipoprotein metabolism and risk of cardiovascular diseases.

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  4 in total

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