Evidence map›Paper›PMID 41776826›Full record

ArticleRheumatology (Oxford, England)2026

Sex differences in clinical and imaging characteristics of axial juvenile spondyloarthritis.

Adam S Mayer, Rui Xiao, Timothy G Brandon, Pamela F Weiss, Juvenile Axial Spondyloarthritis Research Taskforce (JAxSpRT)

Abstract readMulticenter Study
In one paragraph

Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

5 authors.

Adam S MayerDivisions of Adult and Pediatric Rheumatology, Hackensack University Medical Center, Hackensack, NJ, USA.ORCID 0000-0002-2646-0115
Rui XiaoDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-2727-8171
Timothy G BrandonDepartment of Pediatrics, Division of Rheumatology, Children's Hospital of Philadelphia, PA, USA.ORCID 0000-0002-1305-4871
Pamela F WeissDepartment of Pediatrics, Division of Rheumatology, Children's Hospital of Philadelphia, PA, USA.ORCID 0000-0002-9724-0443
Juvenile Axial Spondyloarthritis Research Taskforce (JAxSpRT)

Funding

Training Program/Rheumatic DiseasesT32AR076951 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI EDWARD M BEHRENS, Peter A Merkel · 2020 to 2026
$2.6M
Refining entry criteria and outcome measures for children with axial disease and spondyloarthritis: preparation for clinical trialsR01AR074098 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI WEISS, PAMELA FITCH · 2019 to 2021
$678k
Mentoring and Patient Oriented Research in Juvenile SpondyloarthritisK24AR078950 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI Pamela Fitch Weiss · 2022 to 2026
$664k
National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases Awards 1R01-AR-074098National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases Awards 5T32AR076951-05National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases Awards K24AR078950NIAMS NIH HHS K24 AR078950NIAMS NIH HHS R01 AR074098NIAMS NIH HHS T32 AR076951
6 · The paper itself

Abstract

objectivesThe impact of biologic sex in axial juvenile spondyloarthritis (axJSpA) is unknown. We assessed whether biologic sex is associated with disease manifestations, patient-reported outcomes, or characteristic sacroiliac joint (SIJ) MRI lesions in a large cohort of youths with classified axJSpA.

methodsThis international multicentre cross-sectional study included youths aged <18 years with physician-diagnosed juvenile spondyloarthritis and fulfilling the classification criteria for axJSpA. Clinical and SIJ MRI data were available from the time axial disease was first diagnosed and were compared between males and females using Pearson's chi-squared and Wilcoxon rank-sum tests, as appropriate. Multivariable logistic regression evaluated the association of sex with inflammatory and structural MRI lesions typical of axial disease.

resultsAmong the 143 patients included, 67.1% were male. Males had significantly greater HLA-B27 positivity, hip/groin stiffness and inflammatory marker elevation. There were no differences in peripheral arthritis, enthesitis or patient-reported outcomes. On SIJ MRI, males had significantly higher odds of unequivocal inflammatory lesions (OR 4.86, 95% CI 1.37-17.32), bone marrow oedema (OR 4.13, 95% CI 1.17-14.62) and pelvic enthesitis (OR 5.23, 95% CI 1.39-19.61) compared with females, but no differences in structural lesions were found.

conclusionIn a large multicentre axJSpA cohort, males were significantly more likely to have clinical and MRI features of inflammatory sacroiliitis at the time axial disease was first diagnosed. Future trials in axJSpA should strongly consider stratification by sex in their design.

Indexed as

Axial SpondyloarthritisSacroiliac JointAdolescentChildCross-Sectional StudiesFemaleHLA-B27 AntigenHumansMagnetic Resonance ImagingMaleSex FactorsHLA-B27 Antigenaxial spondyloarthritispaediatricssex

Identifiers

PMID41776826
PMCPMC13007742

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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.