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pmid:29851858

Identification of key genes in rheumatoid arthritis and osteoarthritis based on bioinformatics analysis.

Naiqiang Zhu · Jingyi Hou · Yuanhao Wu · Geng Li · Jinxin Liu · GuiYun Ma · Bin Chen · Youxin Song

Medicine · 2018 doi:10.1097/MD.0000000000010997

Paper

complete

Experiment

complete

Data

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title
Identification of key genes in rheumatoid arthritis and osteoarthritis based on bioinformatics analysis.
doi
10.1097/MD.0000000000010997
pmid
29851858
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Naiqiang Zhu
[1]
Jingyi Hou
[2]
Yuanhao Wu
[3]
Geng Li
[4]
Jinxin Liu
[5]
GuiYun Ma
[6]
Bin Chen
[7]
Youxin Song
journal
Medicine
year
2018
abstract
Rheumatoid arthritis (RA) and osteoarthritis (OA) comprise the most common forms of arthritis. The aim of this study was to identify differentially expressed genes (DEGs) and associated biological processes between RA and OA using a bioinformatics approach to elucidate their potential pathogenesis.The gene expression profiles of the GSE55457 datasets, originally produced through use of the high-throughput Affymetrix Human Genome U133A Array, were downloaded from the Gene Expression Omnibus (GEO) database. The GSE55457 dataset contains information from 33 samples, including 10 normal control (NC) samples, 13 RA samples, and 10 OA samples. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes pathway (KEGG) enrichment analyses were performed to identify functional categories and associated molecular and biochemical pathways, respectively, for the identified DEGs, and a protein-protein interaction (PPI) network of the DEGs was constructed using Cytoscape software.GO and KEGG results suggested that several biological pathways (ie, "immune response," "inflammation," and "osteoclast differentiation") are commonly involved in the development of both RA and OA, whereas several other pathways (eg, "MAPK signaling pathway," and "ECM-receptor interaction") presented significant differences between these disorders.This study provides further insights into the underlying pathogenesis of RA and OA, which may facilitate the diagnosis and treatment of these diseases.
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GO and KEGG results suggested that several biological pathways, including “immune response,” “inflammation,” and “osteoclast differentiation,” are commonly involved in the development of both RA and OA, whereas “MAPK signaling pathway” and “ECM-receptor interaction” presented significant differences between the disorders.
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GO and KEGG results suggested that several biological pathways (ie, “immune response,” “inflammation,” and “osteoclast differentiation”) are commonly involved in the development of both RA and OA, whereas several other pathways (eg, “MAPK signaling pathway,” and “ECM-receptor interaction”) presented significant differences between these disorders.
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GO and KEGG results suggested that several biological pathways, including “immune response,” “inflammation,” and “osteoclast differentiation,” are commonly involved in the development of both RA and OA, whereas “MAPK signaling pathway” and “ECM-receptor interaction” presented significant differences between the disorders.
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Identification of rheumatoid arthritis and osteoarthritis patients by transcriptome-based rule set generation [Jena]
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The aim of this study was to identify differentially expressed genes (DEGs) and associated biological processes between RA and OA using a bioinformatics approach to elucidate their potential pathogenesis.The gene expression profiles of the GSE55457 datasets, originally produced through use of the high-throughput Affymetrix Human Genome U133A Array, were downloaded from the Gene Expression Omnibus (GEO) database. The GSE55457 dataset contains information from 33 samples, including 10 normal control (NC) samples, 13 RA samples, and 10 OA samples. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes pathway (KEGG) enrichment analyses were performed to identify functional categories and associated molecular and biochemical pathways, respectively, for the identified DEGs, and a protein-protein interaction (PPI) network of the DEGs was constructed using Cytoscape software.GO and KEGG results suggested that several biological pathways (ie, \"immune response,\" \"inflammation,\" and \"osteoclast differentiation\") are commonly involved in the development of both RA and OA, whereas several other pathways (eg, \"MAPK signaling pathway,\" and \"ECM-receptor interaction\") presented significant differences between these disorders.This study provides further insights into the underlying pathogenesis of RA and OA, which may facilitate the diagnosis and treatment of these diseases.", "claims": [{"id": "claim-method", "statement": "We used a classical t test to identify DEGs with P < .05 and fold change ≥2 as being statistically significant.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:29851858", "locator": "sections[4] \"Data acquisition and preprocessing\" paragraph 2", "quote": "We used a classical t test to identify DEGs with P < .05 and fold change ≥2 as being statistically significant."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Therefore, in the present study, we downloaded the original data (GSE55457), provided by Dirk Woetzel, from the publically available Gene Expression Omnibus database (GEO, http://www.ncbi.nlm.nih.gov/geo/) to identify DEGs and the associated biological processes between OA and RA using comprehensive bioinformatics analyses.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:29851858", "locator": "sections[1] \"Introduction\" paragraph 4", "quote": "Therefore, in the present study, we downloaded the original data (GSE55457), provided by Dirk Woetzel, from the publically available Gene Expression Omnibus database (GEO, http://www.ncbi.nlm.nih.gov/geo/) to identify DEGs and the associated biological processes between OA and RA using comprehensive bioinformatics analyses."}], "state": "complete"}, {"id": "claim-target-result", "statement": "GO and KEGG results suggested that several biological pathways, including “immune response,” “inflammation,” and “osteoclast differentiation,” are commonly involved in the development of both RA and OA, whereas “MAPK signaling pathway” and “ECM-receptor interaction” presented significant differences between the disorders.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:29851858", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "GO and KEGG results suggested that several biological pathways (ie, “immune response,” “inflammation,” and “osteoclast differentiation”) are commonly involved in the development of both RA and OA, whereas several other pathways (eg, “MAPK signaling pathway,” and “ECM-receptor interaction”) presented significant differences between these disorders."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "GO and KEGG results suggested that several biological pathways, including “immune response,” “inflammation,” and “osteoclast differentiation,” are commonly involved in the development of both RA and OA, whereas “MAPK signaling pathway” and “ECM-receptor interaction” presented significant differences between the disorders.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:29851858"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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