Evidence map›Paper›PMID 25753363›Full record

ArticleBone2015

Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosis.

Sarah S Park, Richard P Beyer, Matthew D Smyth, Christine M Clarke, Andrew E Timms, Theo K Bammler, Brendan D Stamper, Brigham H Mecham, Jennifer A Gustafson, Michael L Cunningham

Open access · greenAbstract read
In one paragraph

Article in Bone, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Genetics versus environment in the pathophysiology of sagittal synostosis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Pooled it
  2. Article
  3. Endoscopic Strip Craniectomy for the Treatment of Single Suture Craniosynostosis.Advances and technical standards in neurosurgery · 2025
    Review
  4. Isolation and Culture of Osteoblasts.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes.International journal of molecular sciences · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

10 authors at 3 institutions in 1 country.

Sarah S ParkSeattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, WA, USA.
Richard P BeyerUniversity of Washington, Center for Ecogenetics and Environmental Health, Seattle, WA, USA.
Matthew D SmythWashington University, Department of Neurosurgery and St. Louis Children's Hospital, St. Louis, MO, USA.
Christine M ClarkeSeattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, WA, USA.
Andrew E TimmsSeattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, WA, USA.
Theo K BammlerUniversity of Washington, Center for Ecogenetics and Environmental Health, Seattle, WA, USA.
Brendan D StamperSchool of Pharmacy, Pacific University, Hillsboro, OR, USA.
Brigham H MechamTrialomics, Seattle, WA, USA.
Jennifer A GustafsonSeattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, WA, USA.
Michael L CunninghamSeattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, WA, USA; Seattle Children's Craniofacial Center, Seattle, WA, USA. Electronic address: mcunning@u.washington.edu.
Center for Environmental Health · USPacific University Oregon · USSt. Louis Children's Hospital · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI GURALNICK, MICHAEL J · 2014 to 2019
$7.9M
SINGLE SUTURE CRANIOSYNOSTOSIS: CANDIDATE GENE AND PATHWAY DISCOVERYR01DE018227 · NIDCR · UNIVERSITY OF WASHINGTON · PI CUNNINGHAM, MICHAEL L · 2008 to 2017
$5.6M
NICHD NIH HHS U54 HD083091NIDCR NIH HHS NIH/NIDCR R01DE018227NIDCR NIH HHS R01 DE018227NIEHS NIH HHS NIH/NIEHS P30ES007033NIEHS NIH HHS P30 ES007033PHS HHS NICHD U54HD083091
6 · The paper itself

Abstract

Single suture craniosynostosis (SSC) is the premature fusion of one calvarial suture and occurs in 1-1700-2500 live births. Congenital fusion of either the sagittal, metopic, or coronal sutures represents 95% of all cases of SSC. Sagittal and metopic synostosis have a male preponderance (3:1) while premature fusion of the coronal suture has a female preponderance (2:1). Although environmental and genetic factors contribute to SSC, the etiology of the majority of SSC cases remains unclear. In this study, 227 primary calvarial osteoblast cell lines from patients with coronal, metopic, or sagittal synostosis and unaffected controls were established and assayed for ALP activity and BrdU incorporation (n = 226) as respective measures of early stage osteoblast differentiation and proliferation. Primary osteoblast cell lines from individuals with sagittal synostosis demonstrated higher levels of ALP activity and reduced proliferation when compared to control lines. In order to address the sex differences in SSC types, the data was further stratified by sex. Osteoblasts from males and females with sagittal synostosis as well as males with metopic synostosis demonstrated higher levels of ALP activity when compared to sex matched controls, and males with sagittal or metopic synostosis demonstrated reduced levels of proliferation. In order to elucidate genes and pathways involved in these observed phenotypes, correlation analyses comparing ALP activity and proliferation to global gene expression was performed. Transcripts related to osteoblast differentiation were identified both differentially up and downregulated, correlated with ALP activity when compared to controls, and demonstrated a striking sex specific gene expression pattern. These data support that the dysregulation of osteoblast differentiation plays a role in the development of SSC and that genetic factors contribute to the observed sex related differences.

Indexed as

Cell DifferentiationGene Expression ProfilingSex FactorsCell ProliferationCells, CulturedCraniosynostosesFemaleHumansMaleOsteoblastsCraniosynostosisGene expression analysisOsteoblast differentiationOsteoblasts

Identifiers

PMID25753363
PMCPMC4546839
OpenAlexW2014710862

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.