Evidence map›Paper›PMID 41063774›Full record

ArticleSmart medicine2025

Contribution of Sex-Biased Expressed Genes in Osteoarthritis.

Cuicui Wang, Meng Shi, Tiandao Li, Shuang Liu, Liang Fang, Ming Xu, Bo Zhang, Jie Shen

Abstract read
In one paragraph

Article in Smart medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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  3. Review
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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

8 authors.

Cuicui WangDepartment of Orthopaedic Surgery School of Medicine Washington University St. Louis Missouri USA.
Meng ShiDepartment of Orthopaedic Surgery School of Medicine Washington University St. Louis Missouri USA.
Tiandao LiDepartment of Developmental Biology Center of Regenerative Medicine Washington University St. Louis Missouri USA.
Shuang LiuDepartment of Orthopaedic Surgery School of Medicine Washington University St. Louis Missouri USA.
Liang FangDepartment of Orthopaedic Surgery School of Medicine Washington University St. Louis Missouri USA.
Ming XuMasonic Institute on the Biology of Aging and Metabolism University of Minnesota Minneapolis Minnesota USA.
Bo ZhangDepartment of Developmental Biology Center of Regenerative Medicine Washington University St. Louis Missouri USA.
Jie ShenDepartment of Orthopaedic Surgery School of Medicine Washington University St. Louis Missouri USA.ORCID https://orcid.org/0000-0003-4131-1211

Funding

Resource Based Center for Musculoskeletal Biology and Medicine (Overall Application)P30AR074992 · NIAMS · WASHINGTON UNIVERSITY · PI MATTHEW J SILVA · 2019 to 2026
$6.8M
Targeting angiogenesis for fracture nonunion treatment under inflammatory diseasesR01AR077616 · NIAMS · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN, SHEN, JIE · 2020 to 2025
$2.7M
Epigenetic Regulation of Bone Regeneration in Inflammatory DiseaseR01AR075860 · NIAMS · WASHINGTON UNIVERSITY · PI SHEN, JIE · 2019 to 2024
$2.6M
Lipid Metabolism in Articular Cartilage and OA PathogenesisR01AR083900 · NIAMS · WASHINGTON UNIVERSITY · PI Jie Shen · 2024 to 2026
$1.9M
Transcriptional regulation of domesticated transposable elements-derived promoters in human genomeR35GM142917 · NIGMS · WASHINGTON UNIVERSITY · PI ZHANG, BO ABER · 2021 to 2025
$1.9M
NIAMS NIH HHS P30 AR074992NIAMS NIH HHS R01 AR075860NIAMS NIH HHS R01 AR077616NIAMS NIH HHS R01 AR083900NIGMS NIH HHS R35 GM142917
6 · The paper itself

Abstract

Human osteoarthritis (OA) displays sex-specific patterns in its clinical presentation. Key features of the disease-such as prevalence, age of onset, progression, and response to treatment-vary between males and females. These differences have been associated with sex hormones, as well as anatomical, biomechanical, and behavioral distinctions between the sexes. However, the underlying mechanisms driving these sex-specific disparities in OA pathogenesis remain largely unknown. In this study, we analyzed transcriptomic data from human knee articular cartilage to investigate sex-specific gene expression in articular chondrocytes. We identified genes that are uniquely or predominantly expressed in either males or females in healthy cartilage. Notably, many of these sex-biased genes were significantly dysregulated in osteoarthritic cartilage, particularly those with higher expression in females. Furthermore, female-specific OA genes may exert protective effects on cartilage degeneration, whereas male-specific OA genes could impair cartilage homeostasis. Our findings provide insights into the genetic regulation of OA and highlight the influence of sex on its molecular pathology.

Indexed as

cartilagehormoneosteoarthritissextranscriptomicstransposable element

Identifiers

PMID41063774
PMCPMC12503069

What OpenQuestion holds

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Registered trials

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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.