Evidence map›Paper›PMID 24928496›Full record

ArticleBone2014

Reduced diaphyseal strength associated with high intracortical vascular porosity within long bones of children with osteogenesis imperfecta.

Carolyne Albert, John Jameson, Peter Smith, Gerald Harris

Open access · greenAbstract read
In one paragraph

Article in Bone, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Mechanical characterization ofCell biomaterials · 2026
    Article
  3. Article
  4. Review
  5. Evaluation of Radiolucent Lesions in Cortices of Long Bones in Osteogenesis Imperfecta Patients.Journal of the Pediatric Orthopaedic Society of North America · 2024
    Article
  6. Review
  7. Article
  8. Antagonism Between PEDF and TGF-β Contributes to Type VI Osteogenesis Imperfecta Bone and Vascular Pathogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  9. Secondary Osteoporosis and Metabolic Bone Diseases.Journal of clinical medicine · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Osteogenesis imperfecta in children and adolescents-new developments in diagnosis and treatment.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
    Review
  18. 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

4 authors at 4 institutions in 1 country.

Carolyne AlbertShriners Hospitals for Children-Chicago, Chicago, IL, USA; Department of Biomedical Engineering, Marquette University, Orthopaedic and Rehabilitation Engineering Center (OREC), Milwaukee, WI, USA. Electronic address: carolyne.albert@marquette.edu.
John JamesonAdvanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA, USA; Department of Biomedical Engineering, Marquette University, Orthopaedic and Rehabilitation Engineering Center (OREC), Milwaukee, WI, USA. Electronic address: john.jameson@marquette.edu.
Peter SmithShriners Hospitals for Children-Chicago, Chicago, IL, USA; Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL, USA. Electronic address: psmith@shrinenet.org.
Gerald HarrisShriners Hospitals for Children-Chicago, Chicago, IL, USA; Department of Biomedical Engineering, Marquette University, Orthopaedic and Rehabilitation Engineering Center (OREC), Milwaukee, WI, USA. Electronic address: gerald.harris@marquette.edu.
Lawrence Berkeley National Laboratory · USMarquette University · USRush University Medical Center · USShriners Hospitals for Children - Chicago · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR031973 · NCRR · MEDICAL COLLEGE OF WISCONSIN · PI SHAKER, REZA NONE · 2010 to 2011
$7.9M
NCRR NIH HHS UL1 RR031973NCRR NIH HHS UL1RR031973
6 · The paper itself

Abstract

Osteogenesis imperfecta is a genetic disorder resulting in bone fragility. The mechanisms behind this fragility are not well understood. In addition to characteristic bone mass deficiencies, research suggests that bone material properties are compromised in individuals with this disorder. However, little data exists regarding bone properties beyond the microstructural scale in individuals with this disorder. Specimens were obtained from long bone diaphyses of nine children with osteogenesis imperfecta during routine osteotomy procedures. Small rectangular beams, oriented longitudinally and transversely to the diaphyseal axis, were machined from these specimens and elastic modulus, yield strength, and maximum strength were measured in three-point bending. Intracortical vascular porosity, bone volume fraction, osteocyte lacuna density, and volumetric tissue mineral density were determined by synchrotron micro-computed tomography, and relationships among these mechanical properties and structural parameters were explored. Modulus and strength were on average 64-68% lower in the transverse vs. longitudinal beams (P<0.001, linear mixed model). Vascular porosity ranged between 3 and 42% of total bone volume. Longitudinal properties were associated negatively with porosity (P≤0.006, linear regressions). Mechanical properties, however, were not associated with osteocyte lacuna density or volumetric tissue mineral density (P≥0.167). Bone properties and structural parameters were not associated significantly with donor age (P≥0.225, linear mixed models). This study presents novel data regarding bone material strength in children with osteogenesis imperfecta. Results confirm that these properties are anisotropic. Elevated vascular porosity was observed in most specimens, and this parameter was associated with reduced bone material strength. These results offer insight toward understanding bone fragility and the role of intracortical porosity on the strength of bone tissue in children with osteogenesis imperfecta.

Indexed as

AdolescentBiomechanical PhenomenaBone and BonesChildChild, PreschoolDiaphysesElastic ModulusFemaleHumansImaging, Three-DimensionalLinear ModelsMaleOsteogenesis ImperfectaPorosityTissue DonorsWeight-BearingFlexural propertiesIntracortical porosityOsteogenesis imperfectaPediatric boneStrength

Identifiers

PMID24928496
PMCPMC4467578
OpenAlexW2170397117

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.