Evidence map›Paper›PMID 28939717›Full record

ArticleJournal of the American Heart Association2017

Apolipoprotein A-I Modulates Atherosclerosis Through Lymphatic Vessel-Dependent Mechanisms in Mice.

Andreea Milasan, Gabriel Jean, François Dallaire, Jean-Claude Tardif, Yahye Merhi, Mary Sorci-Thomas, Catherine Martel

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Lymphatics in Cardiovascular Physiology.Cold Spring Harbor perspectives in medicine · 2022
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. APOA1: a Protein with Multiple Therapeutic Functions.Current atherosclerosis reports · 2021
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Andreea MilasanDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Gabriel JeanDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
François DallaireMontreal Heart Institute, Montreal, Quebec, Canada.
Jean-Claude TardifDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Yahye MerhiDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Mary Sorci-ThomasDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Catherine MartelDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada catherine.martel@icm-mhi.org.
Montreal Heart Institute · CAUniversité de Montréal · CAMedical College of Wisconsin · US

Funding

Biogenesis of HDL Through Cholesterol Efflux and ApoA-I Structural ReorganizationR01HL127649 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI SORCI-THOMAS, MARY G · 2015 to 2018
$2.2M
NHLBI NIH HHS R01 HL127649
6 · The paper itself

Abstract

backgroundSubcutaneously injected lipid-free apoA-I (apolipoprotein A-I) reduces accumulation of lipid and immune cells within the aortic root of hypercholesterolemic mice without increasing high-density lipoprotein-cholesterol concentrations. Lymphatic vessels are now recognized as prerequisite players in the modulation of cholesterol removal from the artery wall in experimental conditions of plaque regression, and particular attention has been brought to the role of the collecting lymphatic vessels in early atherosclerosis-related lymphatic dysfunction. In the present study, we address whether and how preservation of collecting lymphatic function contributes to the protective effect of apoA-I. METHODS AND

resultsAtherosclerotic

conclusionsAltogether, we bring forward a new pleiotropic role for apoA-I in lymphatic function and unveil new potential therapeutic targets for the prevention and treatment of atherosclerosis.

Indexed as

AnimalsAortaAortic DiseasesApolipoprotein A-IAtherosclerosisCells, CulturedDisease Models, AnimalEndothelial CellsFemaleGenetic Predisposition to DiseaseHumansInjections, SubcutaneousLipid MetabolismLymphatic VesselsMice, Inbred C57BLMice, KnockoutAPOA1 protein, humanApolipoprotein A-IFLT4 protein, humanReceptors, LDLVascular Endothelial Growth Factor Receptor-3apolipoprotein A‐Iatherosclerosiscollecting lymphatic vesselsplatelets

Identifiers

PMID28939717
PMCPMC5634311
OpenAlexW2759133973

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.