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pmid:40948653

Identification and molecular mechanism of palmitoylation-related biomarkers in obstructive sleep apnea.

Yiguang Hong · Suyi Zeng · Xueqian Wang · Wei Kang · Bihua Chen · De Lan · Xuemei Wei

Frontiers in neurology · 2025 doi:10.3389/fneur.2025.1499573

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Identification and molecular mechanism of palmitoylation-related biomarkers in obstructive sleep apnea.
doi
10.3389/fneur.2025.1499573
pmid
40948653
authors array · 7 items
[0]
Yiguang Hong
[1]
Suyi Zeng
[2]
Xueqian Wang
[3]
Wei Kang
[4]
Bihua Chen
[5]
De Lan
[6]
Xuemei Wei
journal
Frontiers in neurology
year
2025
abstract
Introduction: Palmitoylation influences patients with obstructive sleep apnea (OSA) by modulating amyloid-β production. However, the involvement of palmitoylation-related genes (PRGs) in OSA remains unclear. This study aims to investigate this mechanism using bioinformatics approaches. Methods: Datasets GSE38792 and GSE135917 were retrieved from the Gene Expression Omnibus (GEO) database. Differentially expressed PRGs (DE-PRGs) were identified through differential expression analysis and weighted gene co-expression network analysis (WGCNA). Candidate genes were pinpointed using the max cluster centrality method in cytoHubba. Biomarkers were selected through machine learning algorithms, expression profiling, and ROC analysis, with diagnostic potential evaluated using a nomogram. Further insights into the role of biomarkers in OSA were provided through enrichment analysis, molecular regulatory network construction, and drug prediction. Results: HIF1A and PDIA3 emerged as potential biomarkers, with the nomogram showing high predictive accuracy for OSA. Enrichment analysis revealed that HIF1A and PDIA3 were co-enriched in pathways such as "focal adhesion," "olfactory transduction," "RNA degradation," "spliceosome," and "ubiquitin-mediated proteolysis." A lncRNA-miRNA-mRNA regulatory network was constructed, featuring multiple regulatory pairs, including CYTOR-hsa-miR-1-3p-HIF1A and CYTOR-hsa-miR-1-3p-PDIA3. Drug prediction analysis identified potential compounds targeting HIF1A, such as klugine, puupehenone, and isocephaeline. Conclusion: HIF1A and PDIA3 were highlighted as significant potential biomarkers, providing valuable insights into the molecular mechanisms of palmitoylation in OSA and potential therapeutic targets.
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Subcutaneous fat transcriptome in obstructive sleep apnea and after treatment with CPAP
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40948653", "kind": "science-record", "revision": 3, "content_hash": "sha256:74c502ff2b0c27bc92cdadf7452f6ae243d488f00dff3173e0d048dade097e99", "created_at": "2026-11-01T20:31:02Z", "updated_at": "2026-11-01T22:14:42Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and molecular mechanism of palmitoylation-related biomarkers in obstructive sleep apnea.", "doi": "10.3389/fneur.2025.1499573", "pmid": "40948653", "authors": ["Yiguang Hong", "Suyi Zeng", "Xueqian Wang", "Wei Kang", "Bihua Chen", "De Lan", "Xuemei Wei"], "journal": "Frontiers in neurology", "year": 2025, "abstract": "Introduction: Palmitoylation influences patients with obstructive sleep apnea (OSA) by modulating amyloid-β production. However, the involvement of palmitoylation-related genes (PRGs) in OSA remains unclear. This study aims to investigate this mechanism using bioinformatics approaches.\nMethods: Datasets GSE38792 and GSE135917 were retrieved from the Gene Expression Omnibus (GEO) database. Differentially expressed PRGs (DE-PRGs) were identified through differential expression analysis and weighted gene co-expression network analysis (WGCNA). Candidate genes were pinpointed using the max cluster centrality method in cytoHubba. Biomarkers were selected through machine learning algorithms, expression profiling, and ROC analysis, with diagnostic potential evaluated using a nomogram. Further insights into the role of biomarkers in OSA were provided through enrichment analysis, molecular regulatory network construction, and drug prediction.\nResults: HIF1A and PDIA3 emerged as potential biomarkers, with the nomogram showing high predictive accuracy for OSA. Enrichment analysis revealed that HIF1A and PDIA3 were co-enriched in pathways such as \"focal adhesion,\" \"olfactory transduction,\" \"RNA degradation,\" \"spliceosome,\" and \"ubiquitin-mediated proteolysis.\" A lncRNA-miRNA-mRNA regulatory network was constructed, featuring multiple regulatory pairs, including CYTOR-hsa-miR-1-3p-HIF1A and CYTOR-hsa-miR-1-3p-PDIA3. Drug prediction analysis identified potential compounds targeting HIF1A, such as klugine, puupehenone, and isocephaeline.\nConclusion: HIF1A and PDIA3 were highlighted as significant potential biomarkers, providing valuable insights into the molecular mechanisms of palmitoylation in OSA and potential therapeutic targets.", "claims": [{"id": "claim-method", "statement": "Differences between groups were analyzed using the Wilcoxon test, with a p-value <0.05 considered statistically significant.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40948653", "locator": "sections[11] \"Statistical analysis\" paragraph 2", "quote": "Differences between groups were analyzed using the Wilcoxon test, with a p-value <0.05 considered statistically significant."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available datasets were analyzed in this study. 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