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Reductions in remnant cholesterol and VLDL cholesterol through inhibition of ANGPTL3 protein synthesis: an analysis from the TRANSLATE-TIMI 70 trial.
Zimerman, Andre; Wiviott, Stephen D; Park, Jeong-Gun; Murphy, Sabina A; Ran, Xinhui; Bramson, Candace R; Curto, Madelyn; Ramos, Vesper; Jevne, Alexandra; Kuder, Julia F; Verma, Subodh; Wojakowski, Wojtek; Terra, Steven G; Sabatine, Marc S; Bergmark, Brian A; Marston, Nicholas A.
Affiliation
  • Zimerman A; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Wiviott SD; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Park JG; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Murphy SA; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Ran X; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Bramson CR; Pfizer, Inc., New York, NY, USA.
  • Curto M; Pfizer, Inc., New York, NY, USA.
  • Ramos V; Pfizer, Inc., New York, NY, USA.
  • Jevne A; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Kuder JF; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Verma S; Department of Surgery, University of Toronto, Toronto, Canada.
  • Wojakowski W; Division of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.
  • Terra SG; Pfizer, Inc., New York, NY, USA.
  • Sabatine MS; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Bergmark BA; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
  • Marston NA; Thrombolysis in Myocardial Infarction (TIMI) Study Group, Brigham and Women's Hospital, Harvard Medical School, 7th Floor, 60 Fenwood Road, Boston, MA 02115, USA.
Eur J Prev Cardiol ; 2024 Mar 14.
Article in En | MEDLINE | ID: mdl-38484368
ABSTRACT

AIMS:

Remnant cholesterol and very low-density lipoprotein cholesterol (VLDL-C) are increasingly recognized risk factors for atherosclerotic disease with few therapeutic options. Angiopoietin-like 3 (ANGPTL3), a key protein in the metabolism of triglyceride-rich lipoproteins, is a promising target. METHODS AND

RESULTS:

TRANSLATE-TIMI 70 was a double-blind, placebo-controlled randomized trial testing seven dose regimens of vupanorsen, an antisense oligonucleotide against ANGPTL3, in adults with non-HDL-C ≥ 100 mg/dL and triglycerides 150-500 mg/dL. The primary endpoint of this analysis was percentage change in remnant cholesterol (total cholesterol minus directly measured LDL-C minus HDL-C) and VLDL-C (directly measured) over 24 weeks. Two hundred eighty-six patients were enrolled, with a median age of 64 years and 44% female. Median baseline remnant cholesterol and VLDL-C were 42 and 31 mg/dL, respectively (reference <30 mg/dL). Vupanorsen lowered remnant cholesterol by 42-59% at 24 weeks over placebo (P < 0.001), achieving a median level of 18 mg/dL at the highest dose. Over the same period, VLDL-C was reduced by 52-67% over placebo (P < 0.001), with a median achieved level of 2.5 mg/dL at the highest dose. The effect of vupanorsen on remnant cholesterol and VLDL-C reduction was dose-dependent and directly associated with the degree of ANGPTL3 inhibition at 90% ANGPTL3 reduction, there was a 61% and 81% decrease in remnant cholesterol and VLDL-C, respectively.

CONCLUSION:

Inhibition of ANGPTL3 protein synthesis significantly lowered remnant cholesterol and VLDL-C in patients with hypertriglyceridaemia. The magnitude of reduction was associated with the degree of ANGPTL3 inhibition. These findings support ANGPTL3 inhibition as a promising target for lowering cholesterol on triglyceride-rich lipoproteins.
In this randomized controlled trial of 286 participants with elevated triglycerides, treatment with vupanorsen, an ANGPTL3 inhibitor, lowered remnant cholesterol by up to 59% and VLDL cholesterol by up to 67% over placebo. The effect of the treatment was sustained throughout 24 weeks and consistent across key patient subgroups. ANGPTL3 inhibition may be a promising approach to treat patients with elevated triglycerides.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur J Prev Cardiol Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur J Prev Cardiol Year: 2024 Document type: Article Affiliation country: United States
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