Evidence map›Paper›PMID 41185046›Full record

ArticleJournal of translational medicine2025

Genomic structural equation modeling decodes skeletal aging: novel loci discovery and multisystem genetic crosstalk.

Yunqiao Zhou, Jian Huang, Leqin Xu, Fan Zhang, Chunxiao Bai, Fangyang Fan, Yuquan Wang, Bixuan Fang, Tian Wang, Xiaohong Mu and 1 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. 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. Mapping the genetic landscape of suicide risk: Insights from genomic SEM.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    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

11 authors.

Yunqiao Zhou *Orthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Jian Huang *Orthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Leqin XuScience and Technology Department, Traditional Chinese Hospital of Xiamen, Xiamen, 361015, China.
Fan ZhangOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Chunxiao BaiOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Fangyang FanOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Yuquan WangOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Bixuan FangOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Tian WangOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China.
Xiaohong MuOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China. muxiaohong2006@163.com.
Jinyu LiOrthopedics Section 1, Dongzhimen Hospital of Beijing University of Chinese Medicine, No. 5 Haiyuncang Hutong, Dongcheng District, Beijing, 100700, China. A03097@bucm.edu.cn.

Funding

Clinical Research Funding for Central Government-Supported High-Level Traditional Chinese Medicine (TCM) Hospitals C2015Excellent Young Scientists Fund of the National Natural Science Foundation of China (NSFC) 82222076Talent Development Program of Dongzhimen Hospital, Beijing University of Chinese Medicine DZMG-LJRC0013
6 · The paper itself

Abstract

objectiveSkeletal aging, a core determinant of systemic aging, poses a global public health challenge due to its association with chronic diseases and functional decline. This study aimed to decode the genetic architecture of skeletal aging by identifying novel loci and multi-system crosstalk using genomic structural equation modeling (Genomic SEM).

methodsWe integrated genome-wide association study (GWAS) data from five musculoskeletal-related traits (osteoporosis [OP], osteoarthritis [OA], lumbar spinal stenosis [LSS], telomere length [TL], and low back pain [LBP]) across 462,933 to 472,174 European individuals. Genomic SEM, FUMA, FUSION, and fine-mapping tools (SuSIE/FINEMAP) were applied to model latent skeletal aging ("mvSAge") and identify causal variants, enriched pathways, and tissue-specific gene expression.

resultsThe latent factor model (CFI = 0.993, SRMR = 0.065) revealed shared genetic architecture among OP, OA, LSS, TL, and LBP. We identified 514 lead SNPs (P < 5 × 10⁻

conclusionThis study establishes mvSAge as a genetically cohesive construct and uncovers novel loci, pathways, and multi-system interactions underlying skeletal aging. These findings advance precision medicine strategies for aging-related musculoskeletal disorders.

Indexed as

AgingBone and BonesGenetic LociGenomicsModels, GeneticGenome-Wide Association StudyHumansPolymorphism, Single NucleotideQuantitative Trait LociGenome-wide association study (GWAS)Genomic structural equation modeling (Genomic SEM)Multi-system crosstalkSkeletal agingWnt signaling

Identifiers

PMID41185046
PMCPMC12581572

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.