Evidence map›Paper›PMID 22005949›Full record

ArticleArthritis and rheumatism2012

Wnt signaling genes of murine chromosome 15 are involved in sex-affected pathways of inflammatory arthritis.

Elena Kudryavtseva, Toni S Forde, Andrew D Pucker, Vyacheslav A Adarichev

Open access · bronzeAbstract read
In one paragraph

Article in Arthritis and rheumatism, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. A novel genomic signature with translational significance for human idiopathic pulmonary fibrosis.American journal of respiratory cell and molecular biology · 2015
    Article
  10. Review
  11. Article
  12. TCDD inhibition of canonical Wnt signaling disrupts prostatic bud formation in mouse urogenital sinus.Toxicological sciences : an official journal of the Society of Toxicology · 2013
    Article
  13. The R-spondin family of proteins: emerging regulators of WNT signaling.The international journal of biochemistry & cell biology · 2012
    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 1 institution in 1 country.

Elena KudryavtsevaAlbert Einstein College of Medicine, Bronx, New York 10461, USA.
Toni S Forde
Andrew D Pucker
Vyacheslav A Adarichev
Albert Einstein College of Medicine · US

Funding

Effects of Sex-Specific Loci in Murine ArthritisR03AR051101 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI ADARICHEV, VYACHESLAV A · 2006 to 2008
$225k
NIAMS NIH HHS AR-051101NIAMS NIH HHS R03 AR051101
6 · The paper itself

Abstract

objectiveSex disparities in rheumatoid arthritis (RA) are well documented despite the lack of any known major RA susceptibility genes mapped to sex chromosomes. Murine chromosome 15 carries the sex-affected Pgia8 locus that mediates proteoglycan-induced arthritis, and homologous human loci are associated with RA. This study was undertaken to identify genes/mechanisms implicated in sex disparities in arthritis.

methodsGene expression analysis was performed using RNA isolated from the paws of male and female Pgia8-congenic mice with collagen antibody-induced arthritis. Results were corroborated by reverse transcription-polymerase chain reaction, and mice were also studied prior to disease onset. Ingenuity Pathways Analysis of the expression patterns and gene functions was used to discover locus-specific and sex-affected signature transcripts.

resultsWe found that the Pgia8 locus regulates antibody-mediated inflammatory arthritis differently in males and females. In Pgia8-congenic males, arthritis severity was 30% less (P < 0.005) than in wild-type males, but the antiinflammatory effect was similar in wild-type and congenic females. Transcriptome analysis indicated that 12 genes within the locus were significantly dysregulated in arthritic joints of congenic mice; expression of these genes was also sex specific. The genes that correlated most highly with arthritis severity included those for collagen triple-helix repeat-containing 1 (Cthrc1), metalloproteinase (Adamts12), R-spondin (Rspo2), and syndecan (Sdc2) (r = 0.87-0.91). The level of Cthrc1 message also correlated with that of the genes for the proinflammatory cytokines interleukin-1β and interleukin-6.

conclusionThese results indicate that sex-specific disparities in RA are linked to transcriptional regulation of genes involved in cartilage degradation (Adamts12) and canonical and noncanonical Wnt signaling (Cthrc1, Rspo2, Sdc2).

Indexed as

AnimalsArthritis, ExperimentalArthritis, RheumatoidChromosomes, Human, Pair 15Disease Models, AnimalFemaleGene ExpressionGenetic Predisposition to DiseaseHumansMaleMiceSeverity of Illness IndexSex FactorsWnt Signaling Pathway

Identifiers

PMID22005949
PMCPMC3288823
OpenAlexW2029942123

What OpenQuestion holds

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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.