Evidence map›Paper›PMID 29960822›Full record

ArticleBiomaterials2018

Settable polymer/ceramic composite bone grafts stabilize weight-bearing tibial plateau slot defects and integrate with host bone in an ovine model.

Sichang Lu, Madison A P McGough, Stefanie M Shiels, Katarzyna J Zienkiewicz, Alyssa R Merkel, Joseph P Vanderburgh, Jeffry S Nyman, Julie A Sterling, David J Tennent, Joseph C Wenke and 1 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2018. 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
1.7field-weighted citation impact, top 17% 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, 21 citations in OpenAlex.

  1. Article
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  3. The dual role of autophagy in periprosthetic osteolysis.Frontiers in cell and developmental biology · 2023
    Review
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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 3 institutions in 1 country.

Sichang LuDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Madison A P McGoughDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Stefanie M ShielsExtremity Trauma and Regenerative Medicine Task Area, U.S. Army Institute of Surgical Research, Fort Sam Houston, TX, USA.
Katarzyna J ZienkiewiczDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Alyssa R MerkelCenter for Bone Biology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, 37235, USA; Department of Veterans Affairs, Nashville, TN, USA.
Joseph P VanderburghDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Jeffry S NymanCenter for Bone Biology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, 37235, USA; Department of Orthopedic Surgery and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN, 37235, USA.
Julie A SterlingCenter for Bone Biology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, 37235, USA; Department of Veterans Affairs, Nashville, TN, USA.
David J TennentExtremity Trauma and Regenerative Medicine Task Area, U.S. Army Institute of Surgical Research, Fort Sam Houston, TX, USA.
Joseph C WenkeExtremity Trauma and Regenerative Medicine Task Area, U.S. Army Institute of Surgical Research, Fort Sam Houston, TX, USA.
Scott A GuelcherDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, 37235, USA; Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA; Center for Bone Biology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, 37235, USA. Electronic address: scott.guelcher@vanderbilt.edu.
Vanderbilt University · USVanderbilt University Medical Center · USUnited States Army Institute of Surgical Research · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Injectable weight-bearing bone grafts for healing of tibial plateau fracturesR01AR064304 · NIAMS · VANDERBILT UNIVERSITY · PI GUELCHER, SCOTT A, WENKE, JOSEPH C · 2013 to 2016
$1.1M
NCI NIH HHS P30 CA068485NEI NIH HHS P30 EY008126NIAMS NIH HHS R01 AR064304NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

Bone fractures at weight-bearing sites are challenging to treat due to the difficulty in maintaining articular congruency. An ideal biomaterial for fracture repair near articulating joints sets rapidly after implantation, stabilizes the fracture with minimal rigid implants, stimulates new bone formation, and remodels at a rate that maintains osseous integrity. Consequently, the design of biomaterials that mechanically stabilize fractures while remodeling to form new bone is an unmet challenge in bone tissue engineering. In this study, we investigated remodeling of resorbable bone cements in a stringent model of mechanically loaded tibial plateau defects in sheep. Nanocrystalline hydroxyapatite-poly(ester urethane) (nHA-PEUR) hybrid polymers were augmented with either ceramic granules (85% β-tricalcium phosphate/15% hydroxyapatite, CG) or a blend of CG and bioactive glass (BG) particles to form a settable bone cement. The initial compressive strength and fatigue properties of the cements were comparable to those of non-resorbable poly(methyl methacrylate) bone cement. In animals that tolerated the initial few weeks of early weight-bearing, CG/nHA-PEUR cements mechanically stabilized the tibial plateau defects and remodeled to form new bone at 16 weeks. In contrast, cements incorporating BG particles resorbed with fibrous tissue filling the defect. Furthermore, CG/nHA-PEUR cements remodeled significantly faster at the full weight-bearing tibial plateau site compared to the mechanically protected femoral condyle site in the same animal. These findings are the first to report a settable bone cement that remodels to form new bone while providing mechanical stability in a stringent large animal model of weight-bearing bone defects near an articulating joint.

Indexed as

AnimalsBone CementsBone TransplantationCeramicsCompressive StrengthFemaleGlassImmunohistochemistryPolymersPolymethyl MethacrylateSheepTibiaWeight-BearingX-Ray Microtomographybioactive glass 45S5Bone CementsPolymersPolymethyl MethacrylateBone cementNanocrystalline hydroxyapatiteTibial fractureWeight bearing fracture

Identifiers

PMID29960822
PMCPMC6065109
OpenAlexW2810244966

What OpenQuestion holds

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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.