Evidence map›Paper›PMID 33029518›Full record

ArticleBioMed research international2020

Functionalized Scaffold and Barrier Membrane with Anti-BMP-2 Monoclonal Antibodies for Alveolar Ridge Preservation in a Canine Model.

Seiko Min, Taewan Kim, Oksu Kim, Carames Goncalo, Tadahiko Utsunomiya, Takashi Matsumoto, Kayo Kuyama, Nikola Angelov

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. [Evaluation of the clinical effect of concentrated growth factor combined with sticky bone in maxillary anterior alveolar ridge preservation].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2025
    Trial
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 5 institutions in 4 countries.

Seiko MinDepartment of Periodontics and Dental Hygiene, University of Texas Health Science Center at Houston, Houston, TX, USA.ORCID https://orcid.org/0000-0003-0716-0616
Taewan KimDepartment of Periodontics, University of Pennsylvania School of Dental Medicine, Philadelphia, PA, USA.
Oksu KimDepartment of Periodontology, Dental Research Institute, School of Dentistry, Chonnam National University, Gwangju, Republic of Korea.
Carames GoncaloDepartment of Periodontology, Implantology Institute, Lisbon, Portugal.
Tadahiko UtsunomiyaDepartment of Pathology, School of Dentistry, Nihon University at Matsudo, Chiba, Japan.
Takashi MatsumotoDivision of Diagnostic Pathology, Nihon University Hospital School of Dentistry at Matsudo, Chiba, Japan.
Kayo KuyamaDepartment of Pathology, School of Dentistry, Nihon University at Matsudo, Chiba, Japan.
Nikola AngelovDepartment of Periodontics and Dental Hygiene, University of Texas Health Science Center at Houston, Houston, TX, USA.
Nihon University · JPThe University of Texas Health Science Center at Houston · USChonnam National University · KRInstituto de Implantologia · PTUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe aim of this study was to investigate the ability of anti-bone morphogenetic protein 2 monoclonal antibody (anti-BMP-2 mAb) to functionalize scaffolds to mediate bone regeneration in a canine model. MATERIALS AND

methodsThe mandibular right premolar 4 (PM4) was extracted in eight beagle dogs and grafted with anti-BMP-2 mAb+anorganic bovine bone mineral with 10% collagen (ABBM-C) and porcine bilayer native collagen membrane (CM). The ABBM-C and CM were functionalized with either anti-BMP-2 mAb (test group) or an isotype matched control mAb (control group). Animals were euthanized at 12 weeks for radiographic, histologic, and histomorphometric analyses. Outcomes were compared between groups.

results3D imaging using cone beam computed tomography (CBCT) revealed that sites treated with ABBM-C and CM functionalized with anti-BMP-2 mAb exhibited significantly more remaining bone width near the alveolar crest, as well as buccal bone height, compared with control groups. Histologic and histomorphometric analyses demonstrated that in anti-BMP-2 mAb-treated sites, total tissue volume was significantly higher in the coronal part of the alveolar bone crest compared with control sites. In anti-BMP-2 mAb-treated sites, bone formation was observed under the barrier membrane.

conclusionFunctionalization of the ABBM-C scaffold and CM appeared to have led to bone formation within healing alveolar bone sockets.

Indexed as

Alveolar ProcessAnatomic LandmarksAnimalsAntibodies, MonoclonalBicuspidBone Morphogenetic Protein 2Cone-Beam Computed TomographyDisease Models, AnimalDogsMandibleMembranesOrgan SizeTissue ScaffoldsAntibodies, MonoclonalBone Morphogenetic Protein 2

Identifiers

PMID33029518
PMCPMC7530509
OpenAlexW3088340449

What OpenQuestion holds

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LicenceCC BY
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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.