Evidence map›Paper›PMID 33722258›Full record

ArticleJournal of orthopaedic surgery and research2021

Machine learning analysis of gene expression profile reveals a novel diagnostic signature for osteoporosis.

Xinlei Chen, Guangping Liu, Shuxiang Wang, Haiyang Zhang, Peng Xue

Abstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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  5. Identification of potential pathogenic genes related to osteoporosis and osteoarthritis.Technology and health care : official journal of the European Society for Engineering and Medicine · 2024
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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

5 authors.

Xinlei ChenDepartment of Orthopedics, Zibo Central Hospital, Zibo, 255000, Shandong, China.
Guangping LiuDepartment of Orthopedics, Zibo Central Hospital, Zibo, 255000, Shandong, China.
Shuxiang WangDepartment of Orthopedics, Zibo Central Hospital, Zibo, 255000, Shandong, China.
Haiyang ZhangDepartment of Orthopedics, Zibo Central Hospital, Zibo, 255000, Shandong, China.
Peng XueDepartment of Orthopedics, Zibo Central Hospital, Zibo, 255000, Shandong, China. xp5879@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteoporosis (OP) is increasingly prevalent with the aging of the world population. It is urgent to identify efficient diagnostic signatures for the clinical application.

methodWe downloaded the mRNA profile of 90 peripheral blood samples with or without OP from GEO database (Number: GSE152073). Weighted gene co-expression network analysis (WGCNA) was used to reveal the correlation among genes in all samples. GO term and KEGG pathway enrichment analysis was performed via the clusterProfiler R package. STRING database was applied to screen the interaction pairs among proteins. Protein-protein interaction (PPI) network was visualized based on Cytoscape, and the key genes were screened using the cytoHubba plug-in. The diagnostic model based on these key genes was constructed, and 5-fold cross validation method was applied to evaluate its reliability.

resultsA gene module consisted of 176 genes predicted to be associated with the occurrence of OP was identified. A total of 16 significantly enriched GO terms and 1 significantly enriched KEGG pathway were obtained based on the 176 genes. The top 50 key genes in the PPI network were identified. Then 22 genes were screened based on stepwise regression analysis from the 50 key genes. Of which, 9 genes were further screened out by multivariate regression analysis with the significant threshold of P value < 0.01. The diagnostic model was established based on the optimal 9 key genes, which efficiently separated the normal samples and OP samples.

conclusionA diagnostic model established based on nine key genes could reliably separate OP patients from healthy subjects, which provided novel lightings on the diagnostic research of OP.

Indexed as

Machine LearningCD5 AntigensFemaleGene Expression ProfilingHumansLogistic ModelsLymphocyte Specific Protein Tyrosine Kinase p56(lck)MaleOsteoporosisPotassium ChannelsProtein Interaction MapsRNA, MessengerSignaling Lymphocytic Activation Molecule FamilyTranscriptomeCD5 AntigensKCTD7 protein, humanLCK protein, humanLY9 protein, humanLymphocyte Specific Protein Tyrosine Kinase p56(lck)Potassium ChannelsRNA, MessengerSignaling Lymphocytic Activation Molecule FamilyLogistic regression modelOsteoporosisPPI networkWGCNA analysis

Identifiers

PMID33722258
PMCPMC7958453

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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.