Evidence map›Paper›PMID 17967568›Full record

ArticleBone2008

Bone microstructure and its associated genetic variability in 12 inbred mouse strains: microCT study and in silico genome scan.

Ilya Sabsovich, J David Clark, Guochun Liao, Gary Peltz, Derek P Lindsey, Christopher R Jacobs, Wei Yao, Tian-Zhi Guo, Wade S Kingery

Open access · greenAbstract read
In one paragraph

Article in Bone, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. A Model of Immediate Implant Placement to Evaluate Early Osseointegration in 129/Sv Diabetic Mice.The International journal of oral & maxillofacial implants · 2023
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  9. Review
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  11. A novel mouse model of intervertebral disc degeneration shows altered cell fate and matrix homeostasis.Matrix biology : journal of the International Society for Matrix Biology · 2018
    Article
  12. Article
  13. Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2016
    Article
  14. The Roles and Mechanisms of Actions of Vitamin C in Bone: New Developments.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2015
    Review
  15. Article
  16. In vivo axial loading of the mouse tibia.Methods in molecular biology (Clifton, N.J.) · 2015
    Article
  17. Article
  18. Article
  19. Adenylyl cyclase 6 mediates loading-induced bone adaptation in vivo.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
  20. 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

9 authors at 3 institutions in 1 country.

Ilya SabsovichPhysical Medicine and Rehabilitation Service, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304, USA. isabo@stanford.edu
J David Clark
Guochun Liao
Gary Peltz
Derek P Lindsey
Christopher R Jacobs
Wei Yao
Tian-Zhi Guo
Wade S Kingery
VA Palo Alto Health Care System · USStanford University · USUniversity of California, Davis · US

Funding

NEURAL REGULATION OF BONE REMODELINGR01DK067197 · NIDDK · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI KINGERY, WADE S · 2004 to 2008
$1.6M
NIDDK NIH HHS DK067197NIDDK NIH HHS R01 DK067197
6 · The paper itself

Abstract

unlabelledMicroCT analysis of 12 inbred strains of mice identified 5 novel chromosomal regions influencing skeletal phenotype. Bone morphology varied in a compartment- and site-specific fashion across strains and genetic influences contributed to the morphometric similarities observed in femoral and vertebral bone within the trabecular bone compartment.

introductionSkeletal development is known to be regulated by both heritable and environmental factors, but whether genetic influence on peak bone mass is site- or compartment-specific is unknown. This study examined the genetic variation of cortical and trabecular bone microarchitecture across 12 strains of mice. MATERIALS AND

methodsMicroCT scanning was used to measure trabecular and cortical bone morphometry in the femur and vertebra of 12 strains of 4-month-old inbred male mice. A computational genome mapping technique was used to identify chromosomal intervals associated with skeletal traits.

resultsSkeletal microarchitecture varied in a compartment- and site-specific fashion across strains. Genome mapping identified 13 chromosomal intervals associated with skeletal traits and 5 of these intervals were novel. Trabecular microarchitecture in different bone sites correlated across strains and most of the chromosomal intervals associated with these trabecular traits were shared between skeletal sites. Conversely, no chromosomal intervals were shared between the trabecular and cortical bone compartments in the femur, even though there was a strong correlation for these different bone compartments across strains, suggesting site-specific regulation by environmental or intrinsic factors.

conclusionIn summary, these data confirm that there are distinct genetic determinants that define the skeletal phenotype at the time when peak bone mass is being acquired, and that genomic regulation of bone morphology is specific for skeletal compartment.

Indexed as

AnimalsBone and BonesComputational BiologyFemaleGenomeMaleMiceMice, Inbred StrainsTomography, X-Ray Computed

Identifiers

PMID17967568
PMCPMC2704123
OpenAlexW1989061098

What OpenQuestion holds

Textmetadata
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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.