Evidence map›Paper›PMID 30074290›Full record

ArticleExperimental dermatology2019

Nail abnormalities identified in an ageing study of 30 inbred mouse strains.

Sarah C Linn, Allison M Mustonen, Kathleen A Silva, Victoria E Kennedy, Beth A Sundberg, Lesley S Bechtold, Sarah Alghamdi, Robert Hoehndorf, Paul N Schofield, John P Sundberg

Open access · greenAbstract read
In one paragraph

Article in Experimental dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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 5 institutions in 3 countries.

Sarah C LinnThe Ohio State University College of Veterinary Medicine, Columbus, Ohio.
Allison M MustonenPurdue University College of Veterinary Medicine, West Lafayette, Indiana.
Kathleen A SilvaThe Jackson Laboratory, Bar Harbor, Maine.
Victoria E KennedyThe Jackson Laboratory, Bar Harbor, Maine.
Beth A SundbergThe Jackson Laboratory, Bar Harbor, Maine.
Lesley S BechtoldThe Jackson Laboratory, Bar Harbor, Maine.
Sarah AlghamdiComputational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.
Robert HoehndorfComputational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.
Paul N SchofieldThe Jackson Laboratory, Bar Harbor, Maine.ORCID 0000-0002-5111-7263
John P SundbergThe Jackson Laboratory, Bar Harbor, Maine.ORCID 0000-0002-1523-5430
Jackson Laboratory · USKing Abdullah University of Science and Technology · SAPurdue University West Lafayette · USThe Ohio State University · USUniversity of Cambridge · GB

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Anna Karolina Palucka · 1985 to 2026
$61.9M
Shock Center for Aging Research at The Jackson Laborato*P30AG025707 · NIA · JACKSON LABORATORY · PI WOYCHIK, RICHARD P · 2005 to 2009
$4.1M
Pathology of Mouse Models of Human DiseaseR13OD010920 · OD · JACKSON LABORATORY · PI SUNDBERG, JOHN PAUL · 2012 to 2021
$200k
NCI NIH HHS CA034196NCI NIH HHS P30 CA034196NIA NIH HHS AG025707NIA NIH HHS P30 AG025707NIH HHS R13 OD010920
6 · The paper itself

Abstract

In a large-scale ageing study, 30 inbred mouse strains were systematically screened for histologic evidence of lesions in all organ systems. Ten strains were diagnosed with similar nail abnormalities. The highest frequency was noted in NON/ShiLtJ mice. Lesions identified fell into two main categories: acute to chronic penetration of the third phalangeal bone through the hyponychium with associated inflammation and bone remodelling or metaplasia of the nail matrix and nail bed associated with severe orthokeratotic hyperkeratosis replacing the nail plate. Penetration of the distal phalanx through the hyponychium appeared to be the initiating feature resulting in nail abnormalities. The accompanying acute to subacute inflammatory response was associated with osteolysis of the distal phalanx. Evaluation of young NON/ShiLtJ mice revealed that these lesions were not often found, or affected only one digit. The only other nail unit abnormality identified was sporadic subungual epidermoid inclusion cysts which closely resembled similar lesions in human patients. These abnormalities, being age-related developments, may have contributed to weight loss due to impacts upon feeding and should be a consideration for future research due to the potential to interact with other experimental factors in ageing studies using the affected strains of mice.

Indexed as

AgingAnimalsBone RemodelingCross-Sectional StudiesEpidermal CystFemaleInflammationKeratin-1Keratin-10KeratosisLongitudinal StudiesMaleMetaplasiaMiceMice, Inbred StrainsNails, MalformedKeratin-1Keratin-10Krt10 protein, mouseKrt1 protein, mousenail dystrophypododermatitis circumscriptasubungual intraosseous epidermoid inclusion cysts

Identifiers

PMID30074290
PMCPMC6360140
OpenAlexW2887970946

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.