Evidence map›Paper›PMID 27610271›Full record

ArticleBioResearch open access2016

Functional Effects of Delivering Human Mesenchymal Stem Cell-Seeded Biological Sutures to an Infarcted Heart.

Katrina J Hansen, John T Favreau, Jacques P Guyette, Ze-Wei Tao, Spencer T Coffin, Anny Cunha-Gavidia, Brian D'Amore, Luke R Perreault, John P Fitzpatrick, Angelica DeMartino and 1 more

Open access · diamondAbstract read
In one paragraph

Article in BioResearch open access, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Biocompatibility of decellularized spinach leaves.npj biomedical innovations · 2025
    Article
  4. Review
  5. A review of current advancements for wound healing: Biomaterial applications and medical devices.Journal of biomedical materials research. Part B, Applied biomaterials · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
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

11 authors at 1 institution in 1 country.

Katrina J HansenDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
John T FavreauDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Jacques P GuyetteDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts.; Center for Regenerative Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Ze-Wei TaoDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts.; Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Spencer T CoffinDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Anny Cunha-GavidiaDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Brian D'AmoreDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Luke R PerreaultDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
John P FitzpatrickDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Angelica DeMartinoDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Glenn R GaudetteDepartment of Biomedical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts.
Worcester Polytechnic Institute · US

Funding

Biological sutures to enhance progenitor cell delivery and retention in the heartR01HL115282 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI GAUDETTE, GLENN R · 2013 to 2017
$1.9M
NHLBI NIH HHS R01 HL115282
6 · The paper itself

Abstract

Stem cell therapy has the potential to improve cardiac function after myocardial infarction (MI); however, existing methods to deliver cells to the myocardium, including intramyocardial injection, suffer from low engraftment rates. In this study, we used a rat model of acute MI to assess the effects of human mesenchymal stem cell (hMSC)-seeded fibrin biological sutures on cardiac function at 1 week after implant. Biological sutures were seeded with quantum dot (Qdot)-loaded hMSCs for 24 h before implantation. At 1 week postinfarct, the heart was imaged to assess mechanical function in the infarct region. Regional parameters assessed were regional stroke work (RSW) and systolic area of contraction (SAC) and global parameters derived from the pressure waveform. MI (n = 6) significantly decreased RSW (0.026 ± 0.011) and SAC (0.022 ± 0.015) when compared with sham operation (RSW: 0.141 ± 0.009; SAC: 0.166 ± 0.005, n = 6) (p < 0.05). The delivery of unseeded biological sutures to the infarcted hearts did not change regional mechanical function compared with the infarcted hearts (RSW: 0.032 ± 0.004, SAC: 0.037 ± 0.008, n = 6). The delivery of hMSC-seeded sutures exerted a trend toward increase of regional mechanical function compared with the infarcted heart (RSW: 0.057 ± 0.011; SAC: 0.051 ± 0.014, n = 6). Global function showed no significant differences between any group (p > 0.05); however, there was a trend toward improved function with the addition of either unseeded or seeded biological suture. Histology demonstrated that Qdot-loaded hMSCs remained present in the infarcted myocardium after 1 week. Analysis of serial sections of Masson's trichrome staining revealed that the greatest infarct size was in the infarct group (7.0% ± 2.2%), where unseeded (3.8% ± 0.6%) and hMSC-seeded (3.7% ± 0.8%) suture groups maintained similar infarct sizes. Furthermore, the remaining suture area was significantly decreased in the unseeded group compared with that in the hMSC-seeded group (p < 0.05). This study demonstrated that hMSC-seeded biological sutures are a method to deliver cells to the infarcted myocardium and have treatment potential.

Indexed as

biomaterialscardiologystem cellstissue engineering

Identifiers

PMID27610271
PMCPMC5003011
OpenAlexW2512355348

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.