Literature DB >> 30155718

The Effect of Bromodomain and Extra-Terminal Inhibitor Apabetalone on Attenuated Coronary Atherosclerotic Plaque: Insights from the ASSURE Trial.

Daisuke Shishikura1, Yu Kataoka1, Satoshi Honda1, Kohei Takata1, Susan W Kim1, Jordan Andrews1, Peter J Psaltis1, Michael Sweeney2, Ewelina Kulikowski2, Jan Johansson2, Norman C W Wong2, Stephen J Nicholls3.   

Abstract

BACKGROUND: Apabetalone is a selective bromodomain and extra-terminal (BET) inhibitor which modulates lipid and inflammatory pathways implicated in atherosclerosis. The impact of apabetalone on attenuated coronary atherosclerotic plaque (AP), a measure of vulnerability, is unknown.
METHODS: The ApoA-1 Synthesis Stimulation and intravascular Ultrasound for coronary atheroma Regression Evaluation (ASSURE; NCT01067820) study employed serial intravascular ultrasound (IVUS) measures of coronary atheroma in 281 patients treated with apabetalone or placebo for 26 weeks. AP was measured at baseline and follow-up. Factors associated with changes in AP were investigated.
RESULTS: AP was observed in 31 patients (11%) [27 (13.0%) in the apabetalone group and four (5.5%) in the placebo group]. The apabetalone group demonstrated reductions in AP length by - 1 mm [interquartile range (IQR) - 4, 1] (p = 0.03), AP arc by - 37.0° (IQR - 59.2, 8.2) (p = 0.003) and the AP index by - 34.6 mm° (IQR - 52.6, 10.1) (p = 0.003) from baseline. The change in AP index correlated with on-treatment concentration of high-density lipoprotein (HDL) particles (r = - 0.52, p = 0.006), but not HDL cholesterol (r = - 0.11, p = 0.60) or apolipoprotein A-1 (r = - 0.16, p = 0.43). Multivariable analysis revealed that on-treatment concentrations of HDL particles (p = 0.03) and very low-density lipoprotein particles (p = 0.01) were independently associated with changes in AP index.
CONCLUSIONS: Apabetalone favorably modulated ultrasonic measures of plaque vulnerability in the population studied, which may relate to an increase in HDL particle concentrations. The clinical implications are currently being investigated in the phase 3 major adverse cardiac event outcomes trial BETonMACE.

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Year:  2019        PMID: 30155718     DOI: 10.1007/s40256-018-0298-8

Source DB:  PubMed          Journal:  Am J Cardiovasc Drugs        ISSN: 1175-3277            Impact factor:   3.571


  9 in total

1.  Effect of Apabetalone Added to Standard Therapy on Major Adverse Cardiovascular Events in Patients With Recent Acute Coronary Syndrome and Type 2 Diabetes: A Randomized Clinical Trial.

Authors:  Kausik K Ray; Stephen J Nicholls; Kevin A Buhr; Henry N Ginsberg; Jan O Johansson; Kamyar Kalantar-Zadeh; Ewelina Kulikowski; Peter P Toth; Norman Wong; Michael Sweeney; Gregory G Schwartz
Journal:  JAMA       Date:  2020-04-28       Impact factor: 56.272

2.  Apabetalone (RVX-208) reduces vascular inflammation in vitro and in CVD patients by a BET-dependent epigenetic mechanism.

Authors:  Laura M Tsujikawa; Li Fu; Shovon Das; Christopher Halliday; Brooke D Rakai; Stephanie C Stotz; Christopher D Sarsons; Dean Gilham; Emily Daze; Sylwia Wasiak; Deborah Studer; Kristina D Rinker; Michael Sweeney; Jan O Johansson; Norman C W Wong; Ewelina Kulikowski
Journal:  Clin Epigenetics       Date:  2019-07-12       Impact factor: 6.551

Review 3.  Histone Deacetylases (HDACs) and Atherosclerosis: A Mechanistic and Pharmacological Review.

Authors:  Xiaona Chen; Yanhong He; Wenjun Fu; Amirhossein Sahebkar; Yuhui Tan; Suowen Xu; Hong Li
Journal:  Front Cell Dev Biol       Date:  2020-11-12

4.  A hierarchical and collaborative BRD4/CEBPD partnership governs vascular smooth muscle cell inflammation.

Authors:  Qingwei Wang; Hatice Gulcin Ozer; Bowen Wang; Mengxue Zhang; Go Urabe; Yitao Huang; K Craig Kent; Lian-Wang Guo
Journal:  Mol Ther Methods Clin Dev       Date:  2021-02-27       Impact factor: 6.698

5.  Inhibition of epigenetic reader proteins by apabetalone counters inflammation in activated innate immune cells from Fabry disease patients receiving enzyme replacement therapy.

Authors:  Li Fu; Sylwia Wasiak; Laura M Tsujikawa; Brooke D Rakai; Stephanie C Stotz; Norman C W Wong; Jan O Johansson; Michael Sweeney; Connie M Mohan; Aneal Khan; Ewelina Kulikowski
Journal:  Pharmacol Res Perspect       Date:  2022-06

6.  Covalent-Fragment Screening of BRD4 Identifies a Ligandable Site Orthogonal to the Acetyl-Lysine Binding Sites.

Authors:  Michael D Olp; Daniel J Sprague; Christopher J Goetz; Stefan G Kathman; Sarah L Wynia-Smith; Shifali Shishodia; Steven B Summers; Ziyang Xu; Alexander V Statsyuk; Brian C Smith
Journal:  ACS Chem Biol       Date:  2020-03-23       Impact factor: 5.100

Review 7.  BET Protein-Mediated Transcriptional Regulation in Heart Failure.

Authors:  Talha Ijaz; Michael A Burke
Journal:  Int J Mol Sci       Date:  2021-06-04       Impact factor: 6.208

Review 8.  Genomic Variants and Multilevel Regulation of ABCA1, ABCG1, and SCARB1 Expression in Atherogenesis.

Authors:  Alexandra V Rozhkova; Veronika G Dmitrieva; Elena V Nosova; Alexander D Dergunov; Svetlana A Limborska; Liudmila V Dergunova
Journal:  J Cardiovasc Dev Dis       Date:  2021-12-02

Review 9.  Targeting epigenetics as atherosclerosis treatment: an updated view.

Authors:  Annette E Neele; Lisa Willemsen; Hung-Jen Chen; Kim E Dzobo; Menno P J de Winther
Journal:  Curr Opin Lipidol       Date:  2020-12       Impact factor: 4.616

  9 in total

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