Evidence map›Paper›PMID 26589134›Full record

ArticleExperimental and molecular pathology2016

Genetic determinants of fibro-osseous lesions in aged inbred mice.

Annerose Berndt, Cheryl Ackert-Bicknell, Kathleen A Silva, Victoria E Kennedy, Beth A Sundberg, Justin M Cates, Paul N Schofield, John P Sundberg

Abstract read
In one paragraph

Article in Experimental and molecular pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis.Mammalian genome : official journal of the International Mammalian Genome Society · 2016
    Article
  7. 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

8 authors at 4 institutions in 2 countries.

Annerose BerndtDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States. Electronic address: berndta@upmc.edu.
Cheryl Ackert-BicknellThe Jackson Laboratory, Bar Harbor, ME, United States. Electronic address: Cheryl_AckertBicknell@URMC.Rochester.edu.
Kathleen A SilvaThe Jackson Laboratory, Bar Harbor, ME, United States. Electronic address: kathleen.silva@jax.org.
Victoria E KennedyThe Jackson Laboratory, Bar Harbor, ME, United States. Electronic address: vicki.kennedy@jax.org.
Beth A SundbergThe Jackson Laboratory, Bar Harbor, ME, United States. Electronic address: beth.sundberg@jax.org.
Justin M CatesDepartment of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN, United States. Electronic address: justin.m.cates@Vanderbilt.Edu.
Paul N SchofieldThe Jackson Laboratory, Bar Harbor, ME, United States; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom. Electronic address: PNS12@cam.ac.uk.
John P SundbergThe Jackson Laboratory, Bar Harbor, ME, United States. Electronic address: john.sundberg@jax.org.
Jackson Laboratory · USUniversity of Cambridge · GBUniversity of Pittsburgh · USVanderbilt University · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Paul Robson · 1985 to 2026
$61.9M
Mouse Models of Human Cancer DatabaseR01CA089713 · NCI · JACKSON LABORATORY · PI BULT, CAROL J · 2002 to 2025
$17.5M
Shock Center for Aging Research at The Jackson Laborato*P30AG025707 · NIA · JACKSON LABORATORY · PI CHURCHILL, GARY A · 2005 to 2009
$4.1M
NCI NIH HHS CA034196NCI NIH HHS CA089713NCI NIH HHS P30 CA034196NCI NIH HHS R01 CA089713NIA NIH HHS AG025707NIA NIH HHS P30 AG025707
6 · The paper itself

Abstract

Fibro-osseous lesions in mice are progressive aging changes in which the bone marrow is replaced to various degrees by fibrovascular stroma and bony trabeculae in a wide variety of bones. The frequency and severity varied greatly among 28 different inbred mouse stains, predominantly affecting females, ranging from 0% for 10 strains to 100% for KK/HlJ and NZW/LacJ female mice. Few lesions were observed in male mice and for 23 of the strains, no lesions were observed in males for any of the cohorts. There were no significant correlations between strain-specific severities of fibro-osseous lesions and ovarian (r=0.11; P=0.57) or endometrial (r=0.03; P=0.89) cyst formation frequency or abnormalities in parathyroid glands. Frequency of fibro-osseous lesions was most strongly associated (P<10(-6)) with genome variations on chromosome (Chr) 8 at 90.6 and 90.8Mb (rs33108071, rs33500669; P=5.0·10(-10), 1.3·10(-6)), Chr 15 at 23.6 and 23.8Mb (rs32087871, rs45770368; P=7.3·10(-7), 2.7·10(-6)), and Chr 19 at 33.2, 33.4, and 33.6Mb (rs311004232, rs30524929, rs30448815; P=2.8·10(-6), 2.8·10(-6), 2.8·10(-6)) in genome-wide association studies (GWAS). The relatively large number of candidate genes identified in the GWAS analyses suggests that this may be an extremely complex polygenic disease. These results indicate that fibro-osseous lesions are surprisingly common in many inbred strains of laboratory mice as they age. While this presents little problem in most studies that utilize young animals, it may complicate aging studies, particularly those focused on bone.

Indexed as

Genome-Wide Association StudyAgingAnimalsBone DiseasesBone MarrowFemaleFibrosisMaleMiceMice, Inbred StrainsRodent DiseasesSex FactorsAgingBoneGenome-wide association studiesKK/HlJ mice

Identifiers

PMID26589134
PMCPMC4766837
OpenAlexW2173619956

What Socratic 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 Socratic graph.