Evidence map›Paper›PMID 25043571›Full record

ArticleBiomaterials2014

ECM hydrogel coating mitigates the chronic inflammatory response to polypropylene mesh.

Denver M Faulk, Ricardo Londono, Matthew T Wolf, Christian A Ranallo, Christopher A Carruthers, Justin D Wildemann, Christopher L Dearth, Stephen F Badylak

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
15.5field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 173 citations in OpenAlex.

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  15. Exploiting Matrix Stiffness to Overcome Drug Resistance.ACS biomaterials science & engineering · 2024
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12 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Denver M FaulkDepartment of Bioengineering, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Ricardo LondonoMcGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; School of Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Matthew T WolfDepartment of Bioengineering, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Christian A RanalloDepartment of Bioengineering, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Christopher A CarruthersDepartment of Bioengineering, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Justin D WildemannDepartment of Bioengineering, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Christopher L DearthMcGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; Department of Surgery, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA.
Stephen F BadylakDepartment of Bioengineering, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA; Department of Surgery, University of Pittsburgh, 450 Technology Drive, Suite 300, Pittsburgh, PA, USA. Electronic address: badylaks@upmc.edu.
University of Pittsburgh · US

Funding

Cardiovascular Bioengineering Training ProgramT32HL076124 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SANJEEV G SHROFF · 2005 to 2026
$7.0M
Engineering a Functional Liver Graft for Treatment of End Stage Liver DiseaseF31AA021324 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FAULK, DENVER MICHAEL · 2012 to 2013
$56k
NHLBI NIH HHS T32 HL076124NHLBI NIH HHS T32-HL76124-6NIAAA NIH HHS 1F31AA021324-01NIAAA NIH HHS F31 AA021324
6 · The paper itself

Abstract

Polypropylene has been used as a surgical mesh material for several decades. This non-degradable synthetic polymer provides mechanical strength, a predictable host response, and its use has resulted in reduced recurrence rates for ventral hernia and pelvic organ prolapse. However, polypropylene and similar synthetic materials are associated with a chronic local tissue inflammatory response and dense fibrous tissue deposition. These outcomes have prompted variations in mesh design to minimize the surface area interface and increase integration with host tissue. In contrast, biologic scaffold materials composed of extracellular matrix (ECM) are rapidly degraded in-vivo and are associated with constructive tissue remodeling and minimal fibrosis. The objective of the present study was to assess the effects of an ECM hydrogel coating on the long-term host tissue response to polypropylene mesh in a rodent model of abdominal muscle injury. At 14 days post implantation, the ECM coated polypropylene mesh devices showed a decreased inflammatory response as characterized by the number and distribution of M1 macrophages (CD86+/CD68+) around mesh fibers when compared to the uncoated mesh devices. At 180 days the ECM coated polypropylene showed decreased density of collagen and amount of mature type I collagen deposited between mesh fibers when compared to the uncoated mesh devices. This study confirms and extends previous findings that an ECM coating mitigates the chronic inflammatory response and associated scar tissue deposition characteristic of polypropylene.

Indexed as

AnimalsBiomechanical PhenomenaChronic DiseaseCoated Materials, BiocompatibleCollagenExtracellular MatrixFluorescent Antibody TechniqueHydrogel, Polyethylene Glycol DimethacrylateImplants, ExperimentalInflammationMacrophagesPhenotypePolypropylenesRatsSurgical MeshSus scrofaCoated Materials, BiocompatibleCollagenHydrogel, Polyethylene Glycol DimethacrylatePolypropylenesCoated surgical meshECM (extracellular matrix)Foreign body responseHydrogelPolypropyleneSurgical mesh

Identifiers

PMID25043571
PMCPMC5942585
OpenAlexW1963795951

What OpenQuestion holds

Textmetadata
LicenceTDM
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.