Why the study?
A trial of vupanorsen reported dose-dependent increases in hepatic fat, leaving it unclear whether this adverse effect is an on-target consequence of inhibiting hepatic ANGPTL3.
Does genetically determined ANGPTL3 deficiency increase the risk of hepatic steatosis?
Does genetically determined ANGPTL3 deficiency increase the risk of hepatic steatosis?
Genetically determined ANGPTL3 deficiency is not associated with hepatic steatosis, suggesting that therapeutic inhibition of ANGPTL3 production in hepatocytes may not inherently cause the hepatic fat accumulation observed with vupanorsen.
Answers are grounded in this paper and cite their sources.
Suggests ANGPTL3 inhibition may avoid steatosis risk; leaves open confirmation in randomized therapeutic trials.
BACKGROUND: ANGPTL3 (angiopoietin-like 3) is a therapeutic target for reducing plasma levels of triglycerides and low-density lipoprotein cholesterol. A recent trial with vupanorsen, an antisense oligonucleotide targeting hepatic production of ANGPTL3, reported a dose-dependent increase in hepatic fat. It is unclear whether this adverse effect is due to an on-target effect of inhibiting hepatic ANGPTL3. METHODS: loss-of-function (LoF) mutations, along with wild-type (WT) participants from 2 previously characterized cohorts located in Campodimele, Italy, and St. Louis, MO. Magnetic resonance spectroscopy and magnetic resonance proton density fat fraction were performed to measure hepatic fat fraction and the distribution of extrahepatic fat. To estimate the causal relationship between ANGPTL3 and hepatic fat, we generated a genetic instrument of plasma ANGPTL3 levels as a surrogate for hepatic protein synthesis and performed Mendelian randomization analyses with hepatic fat in the UK Biobank study. Therapeutic approaches to inhibit ANGPTL3 production in hepatocytes are not necessarily expected to result in the increased risk for hepatic steatosis that was observed with vupanorsen.
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D’Erasmo et al. (2023) studied this question.
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