Evidence map›Paper›PMID 41104785›Full record

ArticleAge and ageing2025

Proteomic profiling of bone tissue reveals distinct pathways in men and women with osteoporosis.

Xiaoyun Lin, Jing Hu, Hengyan Zhang, Lei Sun, Bingna Zhou, Yan Jiang, Ou Wang, Weibo Xia, Jia Zhang, Mei Li

Abstract read
In one paragraph

Article in Age and ageing, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Xiaoyun LinDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Jing HuDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Hengyan ZhangDepartment of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Lei SunDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.ORCID 0000-0002-7864-0337
Bingna ZhouDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Yan JiangDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.ORCID 0000-0003-4434-3462
Ou WangDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.ORCID 0000-0002-0395-8789
Weibo XiaDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.ORCID 0000-0001-7768-5536
Jia ZhangDepartment of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Mei LiDepartment of Endocrinology, National Health Commission Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.ORCID 0000-0001-8634-2252

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteoporosis is characterised by an imbalance in bone remodelling, yet the detailed molecular mechanisms underlying its pathogenesis remain unclear. This study aimed to identify key proteins and regulatory pathways associated with severe osteoporosis in women and men.

methodsBone specimens were collected during surgery from 13 women and 12 men with osteoporotic fractures, along with 8 female and 7 male controls with violent fractures. Differentially abundant proteins (DAPs) in bone tissues were identified via nontargeted liquid chromatography-tandem mass spectrometry proteomics. Functional enrichment and pathway analyses were performed; the diagnostic potential of core DAPs was evaluated through multivariate receiver operating characteristic (ROC) analysis, and correlations between DAPs and clinical parameters were assessed.

resultsDAPs of women with osteoporotic fractures were primarily associated with immunoinflammatory response, while DAPs of men with osteoporotic fractures were predominantly related to oxidative stress. ROC analysis revealed strong associations between core upregulated proteins and osteoporosis in both women [area under the ROC curve (AUC) = 0.908, 95% confidence interval (CI): 0.676-1] and men (AUC = 0.851, 95% CI: 0.366-1). After adjusting for age, HLA-C in women was significantly negatively correlated with bone mineral density (P < .05), while NDUFA11, COX7A2, NDUFAB1, UQCRC1, COX5A and VDAC1 in men were significantly positively correlated with β-C-terminal telopeptide of type I collagen (P < .05).

conclusionThis study identified sex-specific proteomic profiles and molecular pathways associated with osteoporosis, with ageing emerging as a central upstream driver of these differences. These findings may help elucidate the sex differences in the pathogenesis of osteoporosis and provides a foundation for the discovery of new therapeutic targets and the development of personalised precision treatment strategies.

Indexed as

Bone and BonesOsteoporosisOsteoporotic FracturesProteomicsAgedAged, 80 and overBiomarkersBone DensityBone RemodelingCase-Control StudiesFemaleHumansMaleMiddle AgedSex FactorsTandem Mass SpectrometryBiomarkersimmunoinflammatory responseolder peopleosteoporosisoxidative stressproteomics

Identifiers

PMID41104785
PMCPMC12531983

What Socratic holds

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LicenceCC BY
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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 Socratic graph.