Evidence map›Paper›PMID 28515138›Full record

ArticleJournal of lipid research2017

Dalcetrapib and anacetrapib differently impact HDL structure and function in rabbits and monkeys.

Mathieu R Brodeur, David Rhainds, Daniel Charpentier, Teodora Mihalache-Avram, Mélanie Mecteau, Geneviève Brand, Evelyne Chaput, Anne Perez, Eric J Niesor, Eric Rhéaume and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. HDL and Cholesterol Ester Transfer Protein (CETP).Advances in experimental medicine and biology · 2022
    Article
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Mathieu R BrodeurMontreal Heart Institute, Montreal, Quebec, Canada.
David RhaindsMontreal Heart Institute, Montreal, Quebec, Canada.
Daniel CharpentierMontreal Heart Institute, Montreal, Quebec, Canada.
Teodora Mihalache-AvramMontreal Heart Institute, Montreal, Quebec, Canada.
Mélanie MecteauMontreal Heart Institute, Montreal, Quebec, Canada.
Geneviève BrandMontreal Heart Institute, Montreal, Quebec, Canada.
Evelyne ChaputF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Anne PerezF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Eric J NiesorF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Eric RhéaumeMontreal Heart Institute, Montreal, Quebec, Canada; Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Cyrille MaugeaisF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Jean-Claude TardifMontreal Heart Institute, Montreal, Quebec, Canada; Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada. Electronic address: jean-claude.tardif@icm-mhi.org.
Montreal Heart Institute · CARoche (Switzerland) · CHUniversité de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibition of cholesteryl ester transfer protein (CETP) increases HDL cholesterol (HDL-C) levels. However, the circulating CETP level varies and the impact of its inhibition in species with high CETP levels on HDL structure and function remains poorly characterized. This study investigated the effects of dalcetrapib and anacetrapib, the two CETP inhibitors (CETPis) currently being tested in large clinical outcome trials, on HDL particle subclass distribution and cholesterol efflux capacity of serum in rabbits and monkeys. New Zealand White rabbits and vervet monkeys received dalcetrapib and anacetrapib. In rabbits, CETPis increased HDL-C, raised small and large α-migrating HDL, and increased ABCA1-induced cholesterol efflux. In vervet monkeys, although anacetrapib produced similar results, dalcetrapib caused opposite effects because the LDL-C level was increased by 42% and HDL-C decreased by 48% (

Indexed as

AmidesAnimalsApolipoprotein A-IBiological TransportChlorocebus aethiopsCholesterol Ester Transfer ProteinsCholesterol, HDLEstersHep G2 CellsHumansMaleOxazolidinonesRabbitsSpecies SpecificitySulfhydryl CompoundsAmidesanacetrapibApolipoprotein A-ICholesterol Ester Transfer ProteinsCholesterol, HDLdalcetrapibEstersOxazolidinonesSulfhydryl Compoundscholesteryl ester transfer proteineffluxhigh density lipoprotein

Identifiers

PMID28515138
PMCPMC5496027
OpenAlexW2616548027

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.