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pmid:41171455

Identification of potential biomarkers for Lyme disease using bioinformatics and machine learning.

Qi-Wen Lan · Yao-Zhu Wu · Zhi-Shan Wang · Xin-Lei Hu · Yi-Lin Huang · Xun-Jie Cao · Yi-Fei Li · Xu-Guang Guo · Jun-Jie Wang

Clinical and experimental medicine · 2025 doi:10.1007/s10238-025-01803-y

Paper

complete

Experiment

complete

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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pmid:41171455
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title
Identification of potential biomarkers for Lyme disease using bioinformatics and machine learning.
doi
10.1007/s10238-025-01803-y
pmid
41171455
authors array · 9 items
[0]
Qi-Wen Lan
[1]
Yao-Zhu Wu
[2]
Zhi-Shan Wang
[3]
Xin-Lei Hu
[4]
Yi-Lin Huang
[5]
Xun-Jie Cao
[6]
Yi-Fei Li
[7]
Xu-Guang Guo
[8]
Jun-Jie Wang
journal
Clinical and experimental medicine
year
2025
abstract
Lyme disease (LD) presents significant diagnostic challenges due to the absence of a reliable screening method for initial detection. This study aimed to identify potential biomarkers using bioinformatics and machine learning algorithms, which may contribute to future biomarker-based research for Lyme disease diagnostics. The gene expression profile datasets GSE145974 and GSE63085 were analyzed using machine learning to identify hub genes among differentially expressed genes. High-throughput data and receiver operating characteristic curves were used to validate these genes. The molecular mechanisms underlying LD were explored using functional enrichment analysis. The correlation between immune cell counts and insomnia in LD was further validated using clinical data from the GEO database. Gene set enrichment analysis indicated that hub genes were enriched in circadian rhythms. The integration of machine learning revealed FCGR1B, MPP1, and HSPA6 as potential central genes involved in immune response and diagnostic biomarkers for Lyme disease. Immune infiltration analysis showed that LD is frequently associated with the monocyte-macrophage system and humoral immunity. This study provides novel insights into the targeted treatment of LD by revealing novel diagnostic biomarkers.
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Differentially expressed genes (DEGs) were identified using the limma package, applying thresholds of |log2 fold change (logFC)|≥ 1 and adjusted p-value (adj.P) < 0.05 [21].
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sections[4] "Identification of differentially expressed genes (DEGs)" paragraph 2
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Differentially expressed genes (DEGs) were identified using the limma package, applying thresholds of |log2 fold change (logFC)|≥ 1 and adjusted p-value (adj.P) < 0.05 [21].
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The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
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External validation using the GSE63085 dataset confirmed robust diagnostic performance for FCGR1B and MPP1, with AUC values above 0.80 (Fig. 4b).
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sections[15] "Validation of diagnostic performance" paragraph 2
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External validation using the GSE63085 dataset confirmed robust diagnostic performance for FCGR1B and MPP1, with AUC values above 0.80 (Fig. 4b).
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External validation using the GSE63085 dataset confirmed robust diagnostic performance for FCGR1B and MPP1, with AUC values above 0.80 (Fig. 4b).
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Global transcriptome analysis identifies a signature for early disseminated Lyme disease and its resolution
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Identification of a Molecular Signature for Acute Lyme Disease by Human Transcriptome Profiling
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41171455", "kind": "science-record", "revision": 4, "content_hash": "sha256:2ed76d19aac2ba14a7112674137c733ca4dae438d58424a19d4a115dacecf0a4", "created_at": "2026-11-01T20:31:12Z", "updated_at": "2026-11-01T22:57:23Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of potential biomarkers for Lyme disease using bioinformatics and machine learning.", "doi": "10.1007/s10238-025-01803-y", "pmid": "41171455", "authors": ["Qi-Wen Lan", "Yao-Zhu Wu", "Zhi-Shan Wang", "Xin-Lei Hu", "Yi-Lin Huang", "Xun-Jie Cao", "Yi-Fei Li", "Xu-Guang Guo", "Jun-Jie Wang"], "journal": "Clinical and experimental medicine", "year": 2025, "abstract": "Lyme disease (LD) presents significant diagnostic challenges due to the absence of a reliable screening method for initial detection. This study aimed to identify potential biomarkers using bioinformatics and machine learning algorithms, which may contribute to future biomarker-based research for Lyme disease diagnostics. The gene expression profile datasets GSE145974 and GSE63085 were analyzed using machine learning to identify hub genes among differentially expressed genes. High-throughput data and receiver operating characteristic curves were used to validate these genes. The molecular mechanisms underlying LD were explored using functional enrichment analysis. The correlation between immune cell counts and insomnia in LD was further validated using clinical data from the GEO database. Gene set enrichment analysis indicated that hub genes were enriched in circadian rhythms. The integration of machine learning revealed FCGR1B, MPP1, and HSPA6 as potential central genes involved in immune response and diagnostic biomarkers for Lyme disease. Immune infiltration analysis showed that LD is frequently associated with the monocyte-macrophage system and humoral immunity. 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