Evidence map›Paper›PMID 23529475›Full record

ArticleArthritis and rheumatism2013

Testosterone is protective in the sexually dimorphic development of arthritis and lung disease in SKG mice.

Rebecca C Keith, Jeremy Sokolove, Benjamin L Edelman, Lauren Lahey, Elizabeth F Redente, V Michael Holers, Shimon Sakaguchi, William H Robinson, David W H Riches

Open access · greenAbstract read
In one paragraph

Article in Arthritis and rheumatism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
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  14. Exome sequencing link mutation inFrontiers in oncology · 2022
    Article
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  19. Article
  20. Sex, Symptom Severity, and Quality of Life in Rheumatology.Clinical reviews in allergy & immunology · 2019
    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 4 institutions in 2 countries.

Rebecca C KeithNational Jewish Health, Denver, CO 80206, USA.
Jeremy Sokolove
Benjamin L Edelman
Lauren Lahey
Elizabeth F Redente
V Michael Holers
Shimon Sakaguchi
William H Robinson
David W H Riches
University of Colorado Denver · USVA Palo Alto Health Care System · USNational Jewish Health · USOsaka University · JP

Funding

Mechanisms of myofibroblast survival in fibrosisR01HL068628 · NHLBI · NATIONAL JEWISH HEALTH · PI RICHES, DAVID W. · 2002 to 2011
$3.4M
The role TNF-alpha and Macrophages in the Resolution of Pulmonary FibrosisF32HL095274 · NHLBI · NATIONAL JEWISH HEALTH · PI REDENTE, ELIZABETH FRANCES · 2009 to 2011
$151k
NHLBI NIH HHS 1F32-HL-095274NHLBI NIH HHS F32 HL095274NHLBI NIH HHS HL-68628NHLBI NIH HHS R01 HL068628NHLBI NIH HHS T32-HL-00048
6 · The paper itself

Abstract

objectiveRheumatoid arthritis (RA) is a sexually dimorphic inflammatory autoimmune disease with both articular and extraarticular disease manifestations, including RA-associated interstitial lung disease. Low levels of testosterone have been linked to disease severity in men with RA, and supplemental testosterone has been shown to improve RA symptoms in both postmenopausal women and men with low levels of testosterone. The mechanisms by which sex and sex steroids affect the immune system and autoimmunity are poorly understood. The purpose of this study was to examine the protective effects of testicular-derived sex hormones on the development of joint and lung disease in an autoimmune mouse model.

methodsArthritis prevalence and severity were assessed in orchiectomized, sham-orchiectomized, and intact male SKG mice as well as in female SKG mice over a 12-week period after intraperitoneal injection of zymosan. Lung tissues were evaluated by quantifying cellular accumulation in bronchoalveolar lavage fluid, collagen levels, and histologic changes. An antigen microarray was used to evaluate autoantibody generation under each experimental condition.

resultsFemale SKG mice developed arthritis and lung disease at increased prevalence and severity as compared to intact male mice. The absence of testosterone after orchiectomy led to increased arthritis, lung disease, and autoantibody generation in orchiectomized male mice as compared to intact male mice.

conclusionSKG mice represent an authentic sexually dimorphic mouse model of both the joint and lung disease seen in humans with RA. Testosterone protects against the development of joint and lung disease in male SKG mice.

Indexed as

AnimalsArthritis, ExperimentalArthritis, RheumatoidAutoimmunityFemaleLung DiseasesMaleMiceSex CharacteristicsTestosteroneTestosterone

Identifiers

PMID23529475
PMCPMC3672393
OpenAlexW2156087426

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.