Evidence map›Paper›PMID 29946549›Full record

ArticleFrontiers in cardiovascular medicine2018

The BCR-ABL1 Inhibitors Imatinib and Ponatinib Decrease Plasma Cholesterol and Atherosclerosis, and Nilotinib and Ponatinib Activate Coagulation in a Translational Mouse Model.

Marianne G Pouwer, Elsbet J Pieterman, Lars Verschuren, Martien P M Caspers, Cornelis Kluft, Ricardo A Garcia, Jurjan Aman, J Wouter Jukema, Hans M G Princen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Guideline
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  10. Thrombosis in Myeloid Malignancies: From CHIP to AML.Cardiovascular & hematological disorders drug targets · 2024
    Review
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  12. Observational
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  16. Cardiometabolic Consequences of Targeted Anticancer Therapies.Journal of cardiovascular pharmacology · 2022
    Review
  17. Article
  18. Review
  19. Review
  20. 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

9 authors at 5 institutions in 2 countries.

Marianne G PouwerMetabolic Health Research, Gaubius Laboratory, The Netherlands Organization of Applied Scientific Research (TNO), Leiden, Netherlands.
Elsbet J PietermanMetabolic Health Research, Gaubius Laboratory, The Netherlands Organization of Applied Scientific Research (TNO), Leiden, Netherlands.
Lars VerschurenMicrobiology and Systems Biology, The Netherlands Organization of Applied Scientific Research (TNO), Zeist, Netherlands.
Martien P M CaspersMicrobiology and Systems Biology, The Netherlands Organization of Applied Scientific Research (TNO), Zeist, Netherlands.
Cornelis KluftGood Biomarker Sciences, Leiden, Netherlands.
Ricardo A GarciaCardiovascular Drug Discovery, Bristol-Meyers Squibb, New York, United States.
Jurjan AmanDepartments of Physiology and Pulmonary Diseases, VU University Medical Center, Amsterdam, Netherlands.
J Wouter JukemaDepartment of Cardiology, Leiden University Medical Center, Leiden, Netherlands.
Hans M G PrincenMetabolic Health Research, Gaubius Laboratory, The Netherlands Organization of Applied Scientific Research (TNO), Leiden, Netherlands.
Netherlands Organisation for Applied Scientific Research · NLLeiden University Medical Center · NLAmsterdam UMC Location VUmc · NLBristol-Myers Squibb (United States) · USGBS Leiden · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment with the second and third generation BCR-ABL1 tyrosine kinase inhibitors (TKIs) increases cardiovascular risk in chronic myeloid leukemia (CML) patients. We investigated the vascular adverse effects of three generations of TKIs in a translational model for atherosclerosis, the APOE*3Leiden.CETP mouse. Mice were treated for sixteen weeks with imatinib (150 mg/kg BID), nilotinib (10 and 30 mg/kg QD) or ponatinib (3 and 10 mg/kg QD), giving similar drug exposures as in CML-patients. Cardiovascular risk factors were analyzed longitudinally, and histopathological analysis of atherosclerosis and transcriptome analysis of the liver was performed. Imatinib and ponatinib decreased plasma cholesterol (imatinib, -69%,

Indexed as

animal model cardiovascular diseaseatherosclerosiscardiovascular side effectscholesterolchronic myeloid leukemiacoagulation/thrombosislipids and lipoprotein metabolism

Identifiers

PMID29946549
PMCPMC6005845
OpenAlexW2802271217

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.