Evidence map›Paper›PMID 29522281›Full record

ArticleHead & neck2018

Treatment with anti-Sclerostin antibody to stimulate mandibular bone formation.

Matthew Tamplen, Tristan Fowler, Jeffery Markey, P Daniel Knott, Larry J Suva, Tamara Alliston

Open access · greenAbstract read
In one paragraph

Article in Head & neck, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 17 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 2 institutions in 1 country.

Matthew TamplenDepartment of Otolaryngology - Head and Neck Surgery, University of California, San Francisco, California.ORCID 0000-0002-9592-0699
Tristan FowlerDepartment of Orthopedic Surgery, University of California, San Francisco, California.
Jeffery MarkeyDepartment of Otolaryngology - Head and Neck Surgery, University of California, San Francisco, California.
P Daniel KnottDepartment of Otolaryngology - Head and Neck Surgery, University of California, San Francisco, California.
Larry J SuvaDepartment of Veterinary Physiology, Texas A&M University, College Station, Texas.
Tamara AllistonDepartment of Otolaryngology - Head and Neck Surgery, University of California, San Francisco, California.
University of California, San Francisco · USTexas A&M University · US

Funding

The mechanistic control of bone quality and joint crosstalk by osteocytesR01DE019284 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, CHRISTOPHER JOHN · 2009 to 2024
$7.6M
Skeletal Biology and Biomechanics (SBB) CoreP30AR075055 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Wenhan Chang · 2019 to 2026
$7.1M
UCSF Core Center for Musculoskeletal Biology and MedicineP30AR066262 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOTZ, JEFFREY C. · 2014 to 2018
$3.0M
ROLE OF OSTEOCYTE TbetaRII IN PERILACUNAR REMODELING AND BONE METASTASESF32CA203402 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FOWLER, TRISTAN WILLIAM · 2016 to 2016
$16k
NCI NIH HHS F32 CA203402NIAMS NIH HHS P30 AR066262NIAMS NIH HHS P30 AR075055NIDCR NIH HHS R01 DE019284
6 · The paper itself

Abstract

backgroundAnti-Sclerostin antibody (Scl-Ab) is a promising new bone anabolic therapy. Although anti-Scl-Ab stimulates bone formation and repair in the appendicular and axial skeleton, its efficacy in the craniofacial skeleton is still poorly understood.

methodsUsing an established model of Down syndrome-dependent bone deficiency, 10 Ts65Dn mice and 10 wild-type mice were treated weekly via i.v. tail vein injection with vehicle or anti-Sclerostin for 3 weeks and euthanized 1 week after.

resultsWild-type mice treated with the anti-Scl-Ab had increased mandibular bone, trabecular thickness, and alveolar height compared with controls. Anti-Scl-Ab increased Ts65Dn mandibular bone parameters such that they were statistically indistinguishable from those in vehicle-treated wild-type mandibles.

conclusionTreatment with anti-Scl-Ab significantly increased mandibular bone mass and alveolar height in wild type mice and normalized mandibular bone mass and alveolar height in Ts65Dn mice. The anti-Scl-Ab therapy represents a novel method for increasing mandibular bone formation.

Indexed as

Adaptor Proteins, Signal TransducingAlveolar ProcessAnimalsAntibodiesBone Morphogenetic ProteinsDisease Models, AnimalGlycoproteinsIntercellular Signaling Peptides and ProteinsMandibleMice, Mutant StrainsOsteogenesisAdaptor Proteins, Signal TransducingAntibodiesBone Morphogenetic ProteinsGlycoproteinsIntercellular Signaling Peptides and ProteinsSost protein, mousehead and neck reconstructionmandiblemicro-CTosteoradionecrosissclerostin

Identifiers

PMID29522281
PMCPMC6037571
OpenAlexW2792839668

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.