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: We recruited participants with ANGPTL3 deficiency related to ANGPTL3 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. Results: We recruited participants with complete (n=6) or partial (n=32) ANGPTL3 deficiency related to ANGPTL3 LoF mutations, as well as WT participants (n=92) without LoF mutations. Participants with ANGPTL3 deficiency exhibited significantly lower total cholesterol (complete deficiency, 78.5 mg/dL; partial deficiency, 172 mg/dL; WT, 188 mg/dL; P<0.05 for both deficiency groups compared with WT), along with plasma triglycerides (complete deficiency, 26 mg/dL; partial deficiency, 79 mg/dL; WT, 88 mg/dL; P<0.05 for both deficiency groups compared with WT) without any significant difference in hepatic fat (complete deficiency, 9.8%; partial deficiency, 10.1%; WT, 9.9%; P>0.05 for both deficiency groups compared with WT) or severity of hepatic steatosis as assessed by magnetic resonance imaging. In addition, ANGPTL3 deficiency did not alter the distribution of extrahepatic fat. Results from Mendelian randomization analyses in 36 703 participants from the UK Biobank demonstrated that genetically determined ANGPTL3 plasma protein levels were causally associated with low-density lipoprotein cholesterol (P=1.7×10-17) and triglycerides (P=3.2×10-18) but not with hepatic fat (P=0.22). Conclusions: ANGPTL3 deficiency related to LoF mutations in ANGPTL3, as well as genetically determined reduction of plasma ANGPTL3 levels, is not associated with hepatic steatosis. 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.

ANGPTL3 Deficiency and Risk of Hepatic Steatosis / D'Erasmo, Laura; Di Martino, Michele; Neufeld, Thomas; Fraum, Tyler J; Kang, Chul Joo; Burks, Kendall H; Di Costanzo, Alessia; Minicocci, Ilenia; Bini, Simone; Maranghi, Marianna; Pigna, Giovanni; Labbadia, Giancarlo; Zheng, Jie; Fierro, Davide; Montali, Anna; Ceci, Fabrizio; Catalano, Carlo; Davidson, Nicholas O; Lucisano, Giuseppe; Nicolucci, Antonio; Arca, Marcello; Stitziel, Nathan O. - In: CIRCULATION. - ISSN 0009-7322. - 148:19(2023), pp. 1479-1489. [10.1161/CIRCULATIONAHA.123.065866]

ANGPTL3 Deficiency and Risk of Hepatic Steatosis

D'Erasmo, Laura;Di Costanzo, Alessia;Minicocci, Ilenia;Bini, Simone;Maranghi, Marianna;Labbadia, Giancarlo;Ceci, Fabrizio;Catalano, Carlo;Arca, Marcello;
2023

Abstract

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: We recruited participants with ANGPTL3 deficiency related to ANGPTL3 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. Results: We recruited participants with complete (n=6) or partial (n=32) ANGPTL3 deficiency related to ANGPTL3 LoF mutations, as well as WT participants (n=92) without LoF mutations. Participants with ANGPTL3 deficiency exhibited significantly lower total cholesterol (complete deficiency, 78.5 mg/dL; partial deficiency, 172 mg/dL; WT, 188 mg/dL; P<0.05 for both deficiency groups compared with WT), along with plasma triglycerides (complete deficiency, 26 mg/dL; partial deficiency, 79 mg/dL; WT, 88 mg/dL; P<0.05 for both deficiency groups compared with WT) without any significant difference in hepatic fat (complete deficiency, 9.8%; partial deficiency, 10.1%; WT, 9.9%; P>0.05 for both deficiency groups compared with WT) or severity of hepatic steatosis as assessed by magnetic resonance imaging. In addition, ANGPTL3 deficiency did not alter the distribution of extrahepatic fat. Results from Mendelian randomization analyses in 36 703 participants from the UK Biobank demonstrated that genetically determined ANGPTL3 plasma protein levels were causally associated with low-density lipoprotein cholesterol (P=1.7×10-17) and triglycerides (P=3.2×10-18) but not with hepatic fat (P=0.22). Conclusions: ANGPTL3 deficiency related to LoF mutations in ANGPTL3, as well as genetically determined reduction of plasma ANGPTL3 levels, is not associated with hepatic steatosis. 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.
2023
angiopoietin-like protein 3; fatty acids, nonesterified; fatty liver; lipids; magnetic resonance spectroscopy; triglycerides
01 Pubblicazione su rivista::01a Articolo in rivista
ANGPTL3 Deficiency and Risk of Hepatic Steatosis / D'Erasmo, Laura; Di Martino, Michele; Neufeld, Thomas; Fraum, Tyler J; Kang, Chul Joo; Burks, Kendall H; Di Costanzo, Alessia; Minicocci, Ilenia; Bini, Simone; Maranghi, Marianna; Pigna, Giovanni; Labbadia, Giancarlo; Zheng, Jie; Fierro, Davide; Montali, Anna; Ceci, Fabrizio; Catalano, Carlo; Davidson, Nicholas O; Lucisano, Giuseppe; Nicolucci, Antonio; Arca, Marcello; Stitziel, Nathan O. - In: CIRCULATION. - ISSN 0009-7322. - 148:19(2023), pp. 1479-1489. [10.1161/CIRCULATIONAHA.123.065866]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1692967
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