Evidence map›Paper›PMID 31815824›Full record

ArticleJournal of cardiovascular pharmacology2020

Administration of Interleukin-15 Peptide Improves Cardiac Function in a Mouse Model of Myocardial Infarction.

Kurosh Ameri, Dulguun Bayardorj, Raffi Samurkashian, Maxwell Fredkin, Eric Fuh, Vien Nguyen, Yerem Yeghiazarians

Open access · hybridAbstract read
In one paragraph

Article in Journal of cardiovascular pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Role of interleukin-15 in cardiovascular diseases.Journal of cellular and molecular medicine · 2020
    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 4 institutions in 1 country.

Kurosh AmeriDepartment of Medicine, Division of Cardiology, Cardiovascular Research Institute, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA.
Dulguun BayardorjDepartment of Medicine, Division of Cardiology, Cardiovascular Research Institute, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA.
Raffi SamurkashianDepartment of Biomedical Engineering, University of California, Davis, Davis, CA; and.
Maxwell FredkinDepartment of Medicine, Division of Cardiology, Cardiovascular Research Institute, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA.
Eric FuhPermanente Medical Group, Santa Clara, CA.
Vien NguyenDepartment of Medicine, Division of Cardiology, Cardiovascular Research Institute, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA.
Yerem YeghiazariansDepartment of Medicine, Division of Cardiology, Cardiovascular Research Institute, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA.
University of California, San Francisco · USBroad Center · USColorado Permanente Medical Group · USUniversity of California, Davis · US

Funding

SFSU MA-MS/PHD BRIDGE TO THE FUTURER25GM048972 · NIGMS · SAN FRANCISCO STATE UNIVERSITY · PI BAYLISS, FRANK T, FUSE, MEGUMI M. · 1992 to 2020
$5.6M
NIGMS NIH HHS R25 GM048972
6 · The paper itself

Abstract

Interleukin-15 is a pleotropic factor, capable of modulating metabolism, survival, proliferation, and differentiation in many different cell types. The rationale behind this study relates to previous work demonstrating that IL-15 is a major factor present in stem cell extracts, which protects cardiomyocytes subjected to hypoxic stress in vitro. The objective of this current study was to assess whether administration of IL-15 peptide will also show protective effects in vivo. The data indicate that administration of IL-15 reduces cell death, increases vascularity, decreases scar size, and significantly improves left ventricular ejection fraction in a mouse model of myocardial infarction.

Indexed as

AnimalsCardiovascular AgentsCell DeathCells, CulturedDisease Models, AnimalHumansHuman Umbilical Vein Endothelial CellsInterleukin-15MaleMice, Inbred C57BLMyocardial InfarctionMyocytes, CardiacNeovascularization, PhysiologicRecovery of FunctionStroke VolumeVentricular Function, LeftCardiovascular AgentsInterleukin-15

Identifiers

PMID31815824
PMCPMC6964872
OpenAlexW2996691233

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.