Evidence map›Paper›PMID 30479835›Full record

ArticleBDJ open2018

Transcriptomic profiling of tantalum metal implant osseointegration in osteopenic patients.

E K Hefni, S Bencharit, S J Kim, K M Byrd, T Moreli, F H Nociti, S Offenbacher, S P Barros

Open access · goldAbstract read
In one paragraph

Article in BDJ open, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

8 authors at 3 institutions in 2 countries.

E K Hefni1Department of Periodontology, School of Dentistry, University of North Carolina, Chapel Hill, NC USA.ORCID 0000-0003-3920-2120
S Bencharit2Department of General Practice, School of Dentistry, Virginia Commonwealth University, Richmond, VA USA.
S J Kim1Department of Periodontology, School of Dentistry, University of North Carolina, Chapel Hill, NC USA.
K M Byrd1Department of Periodontology, School of Dentistry, University of North Carolina, Chapel Hill, NC USA.
T Moreli1Department of Periodontology, School of Dentistry, University of North Carolina, Chapel Hill, NC USA.
F H Nociti3Department of Periodontology, School of Dentistry, State University of Campinas, Campinas, Brazil.
S Offenbacher1Department of Periodontology, School of Dentistry, University of North Carolina, Chapel Hill, NC USA.
S P Barros1Department of Periodontology, School of Dentistry, University of North Carolina, Chapel Hill, NC USA.
University of North Carolina at Chapel Hill · USUniversidade Estadual de Campinas (UNICAMP) · BRVirginia Commonwealth University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe long-term success of dental implants is established by literature. Although clinically well defined, the complex genetic pathways underlying osseointegration have not yet been fully elucidated. Furthermore, patients with osteopenia/osteoporosis are considered to present as higher risk for implant failure. Porous tantalum trabecular metal (PTTM), an open-cell porous biomaterial, is suggested to present enhanced biocompatibility and osteoconductivity. The goal of this study was to evaluate the expression patterns of a panel of genes closely associated with osteogenesis and wound healing in osteopenic patients receiving either traditional titanium (Ti) or PTTM cylinders to assess the pathway of genes activation in the early phases of osseointegration. MATERIAL AND

methodsImplant cylinders made of Ti and PTTM were placed in osteopenic volunteers. At 2- and 4 weeks of healing, one Ti and one PTTM cylinder were removed from each subject for RT-PCR analysis using osteogenesis PCR array.

resultsCompared to Ti, PTTM-associated bone displayed upregulation of bone matrix proteins, BMP/TGF tisuperfamily, soluble ligand and integrin receptors, growth factors, and collagen genes at one or both time points. Histologically, PTTM implants displayed more robust osteogenesis deposition and maturity when compared to Ti implants from the same patient.

conclusionsOur results indicate that PTTM properties could induce an earlier activation of genes associated with osteogenesis in osteopenic patients suggesting that PTTM implants may attenuate the relative risk of placing dental implants in this population.

Identifiers

PMID30479835
PMCPMC6251902
OpenAlexW2901708082

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Registered trials

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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.