Evidence map›Paper›PMID 26446504›Full record

ArticleJournal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie2015

Effect of compressive loading and incubation with clodronate on the RANKL/OPG system of human osteoblasts.

Sarah Grimm, Christian Walter, Andreas Pabst, Jutta Goldschmitt, Heinrich Wehrbein, Collin Jacobs

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In one paragraph

Article in Journal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 97% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Sarah GrimmDepartment of Orthodontics, Johannes Gutenberg University, Augustusplatz 2, 55131, Mainz, Germany. sarah.grimm@unimedizin-mainz.de.
Christian WalterDepartment of Oral an Maxillofacial Surgery, Johannes Gutenberg University, Mainz, Germany.
Andreas PabstDepartment of Oral an Maxillofacial Surgery, Johannes Gutenberg University, Mainz, Germany.
Jutta GoldschmittDepartment of Oral an Maxillofacial Surgery, Johannes Gutenberg University, Mainz, Germany.
Heinrich WehrbeinDepartment of Orthodontics, Johannes Gutenberg University, Augustusplatz 2, 55131, Mainz, Germany.
Collin JacobsDepartment of Orthodontics, Johannes Gutenberg University, Augustusplatz 2, 55131, Mainz, Germany.
Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn vivo studies have shown that bisphosphonates result in slow rates of orthodontic tooth movement. This study investigated whether clodronate modifies the impact of mechanical loading on the RANKL/OPG system of human osteoblasts.

methodsOsteoblasts were cultured in vitro with 0.5 or 5.0 µM clodronate for 48 h and/or subjected to 3 h of compressive loading at 34.9 g/cm(2). Cell viability was determined by MTT assay. Real-time polymerase chain reaction (PCR), enzyme-linked immunosorbent assay (ELISA), and immunocytochemical staining were used to analyze the cells for their production of osteoprotegerin (OPG) and receptor activator of nuclear factor kappa-B ligand (RANKL) at the transcriptional and protein levels.

resultsCompressive loading did not affect osteoblast viability in a significant way. Clodronate (5.0 µM) mildly reduced the viability of both compressed and uncompressed cells. Compressive loading induced a 4.2-fold increase in RANKL gene expression, while clodronate led to a concentration-dependent inhibition of this effect (1.8-fold increase at 5.0 µM). OPG gene expression was decreased by compressive loading both in the presence of 0.5 µM clodronate and in the absence of clodronate, and OPG protein synthesis in the compressed cells was significantly decreased in the presence of clodronate. Immunocytochemical staining revealed an increase of RANKL protein synthesis in compressed cells, while clodronate and cell compression reduced this increase.

conclusionThis study demonstrates that clodronate decreases the compression-induced RANKL/OPG ratio expressed by human osteoblasts. Reported in vivo findings of reduced osteoclast numbers on the compression side of orthodontic tooth movement under the action of clodronate-and the associated slow rate of tooth movement-might be attributable not only to a direct impact on osteoclasts but also to changes in osteoblast-osteoclast interaction resulting from the presence of clodronate.

Indexed as

Bone Density Conservation AgentsCells, CulturedCell SurvivalClodronic AcidCompressive StrengthDose-Response Relationship, DrugHumansMechanotransduction, CellularOsteoblastsOsteoprotegerinRANK LigandStress, MechanicalWeight-BearingBone Density Conservation AgentsClodronic AcidOsteoprotegerinRANK LigandTNFSF11 protein, humanBisphosphonatesMechanical loadingOrthodontic tooth movementRANKL/OPG systemRoot resorption

Identifiers

PMID26446504
OpenAlexW1821160520

What OpenQuestion holds

Textmetadata
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.