Evidence map›Paper›PMID 23536112›Full record

ArticleAnnals of biomedical engineering2013

Gender-dependence of bone structure and properties in adult osteogenesis imperfecta murine model.

Xiaomei Yao, Stephanie M Carleton, Arin D Kettle, Jennifer Melander, Charlotte L Phillips, Yong Wang

Open access · greenAbstract read
In one paragraph

Article in Annals of biomedical engineering, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 65 citations in OpenAlex.

  1. Iron overload induced by ferric derisomaltose and ferric carboxymaltose both increase FGF-23 levels and lead to osteomalacia and bone loss in normal mice.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Article
  2. Review
  3. Article
  4. Cardiac health, type I collagen, and aging in theAmerican journal of physiology. Heart and circulatory physiology · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Sexing Bones: Improving Transparency of Sex Reporting to Address Bias Within Preclinical Studies.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Intrafibrillar mineralization deficiency and osteogenesis imperfecta mouse bone fragility.Journal of the mechanical behavior of biomedical materials · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Fecundity is impaired in a mouse model of osteogenesis imperfecta.Molecular reproduction and development · 2020
    Article
  18. TGFβ Regulation of Perilacunar/Canalicular Remodeling Is Sexually Dimorphic.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  19. Article
  20. Article
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.

Xiaomei YaoDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri-Kansas City, 650 E. 25th St., Kansas City, MO 64108, USA.
Stephanie M Carleton
Arin D Kettle
Jennifer Melander
Charlotte L Phillips
Yong Wang
University of Missouri · USUniversity of Missouri–Kansas City · US

Funding

Mechanotransduction Approach to Improve Bone Quality in Osteogenesis ImperfectaR01AR055907 · NIAMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI PHILLIPS, CHARLOTTE L · 2010 to 2012
$974k
NIAMS NIH HHS R01 AR055907NIAMS NIH HHS R01AR055907
6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) is a dominant skeletal disorder characterized by bone fragility and deformities. Though the oim mouse model has been the most widely studied of the OI models, it has only recently been suggested to exhibit gender-dependent differences in bone mineralization. To characterize the impact of gender on the morphometry/ultra-structure, mechanical properties, and biochemical composition of oim bone on the congenic C57BL/J6 background, 4-month-old oim/oim, +/oim, and wild-type (wt) female and male tibiae were evaluated using micro-computed tomography, three-point bending, and Raman spectroscopy. Dramatic gender differences were evident in both cortical and trabecular bone morphological and geometric parameters. Male mice had inherently more bone and increased moment of inertia than genotype-matched female counterparts with corresponding increases in bone biomechanical strength. The primary influence of gender was structure/geometry in bone growth and mechanical properties, whereas the mineral/matrix composition and hydroxyproline content of bone were influenced primarily by the oim collagen mutation. This study provides evidence of the importance of gender in the evaluation and interpretation of potential therapeutic strategies when using mouse models of OI.

Indexed as

AnimalsBiomechanical PhenomenaCarbonatesDisease Models, AnimalElastic ModulusFemaleHydroxyprolineMaleMiceMice, Inbred C57BLMice, TransgenicOsteogenesisOsteogenesis ImperfectaPhosphatesSex FactorsSpectrum Analysis, RamanCarbonatesHydroxyprolinePhosphates

Identifiers

PMID23536112
PMCPMC3703620
OpenAlexW1995835293

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.