Evidence map›Paper›PMID 23801661›Full record

ArticleJournal of lipid research2013

Antisense oligonucleotide inhibition of cholesteryl ester transfer protein enhances RCT in hyperlipidemic, CETP transgenic, LDLr-/- mice.

Thomas A Bell, Mark J Graham, Richard G Lee, Adam E Mullick, Wuxia Fu, Dan Norris, Rosanne M Crooke

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Very low HDL levels: clinical assessment and management.Archives of endocrinology and metabolism · 2023
    Review
  3. Review
  4. Article
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  8. Article
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  10. Article
  11. HDL-targeted therapies: progress, failures and future.Nature reviews. Drug discovery · 2014
    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

7 authors at 1 institution in 1 country.

Thomas A BellCardiovascular Antisense Drug Discovery Group, Isis Pharmaceuticals, Inc., Carlsbad, CA 92010.
Mark J Graham
Richard G Lee
Adam E Mullick
Wuxia Fu
Dan Norris
Rosanne M Crooke
Ionis Pharmaceuticals (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to their ability to promote positive effects across all of the lipoprotein classes, cholesteryl ester transfer protein (CETP) inhibitors are currently being developed as therapeutic agents for cardiovascular disease. In these studies, we compared an antisense oligonucleotide (ASO) inhibitor of CETP to the CETP small molecule inhibitor anacetrapib. In hyperlipidemic CETP transgenic (tg) mice, both drugs provided comparable reductions in total plasma cholesterol, decreases in CETP activity, and increases in HDL cholesterol. However, only mice treated with the antisense inhibitor showed an enhanced effect on macrophage reverse cholesterol transport, presumably due to differences in HDL apolipoprotein composition and decreases in plasma triglyceride. Additionally, the ASO-mediated reductions in CETP mRNA were associated with less accumulation of aortic cholesterol. These preliminary findings suggest that CETP ASOs may represent an alternative means to inhibit that target and to support their continued development as a treatment for cardiovascular disease in man.

Indexed as

AnimalsAnticholesteremic AgentsAortaBiological TransportCardiovascular DiseasesCholesterol Ester Transfer ProteinsCholesterol, HDLCombined Modality TherapyGene ExpressionGene Knockdown TechniquesHyperlipidemiasLipoproteins, LDLLiverMacrophagesMaleMiceanacetrapibAnticholesteremic AgentsCholesterol Ester Transfer ProteinsCholesterol, HDLLipoproteins, LDLOligonucleotides, AntisenseOxazolidinonesReceptors, LDLTriglyceridescardiovascular diseasecholesteryl ester transfer proteinlipoprotein metabolismlow density lipoprotein

Identifiers

PMID23801661
PMCPMC3770078
OpenAlexW2148059307

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.