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pmid:39026189

Coronavirus disease 2019-related myocarditis genes contribute to ECMO prognosis.

An Yan · Ruiying Zhang · Chao Feng · Jinping Feng

BMC cardiovascular disorders · 2024 doi:10.1186/s12872-024-04032-5

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

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pmid:39026189
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2026-11-01T20:29:06Z
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title
Coronavirus disease 2019-related myocarditis genes contribute to ECMO prognosis.
doi
10.1186/s12872-024-04032-5
pmid
39026189
authors array · 4 items
[0]
An Yan
[1]
Ruiying Zhang
[2]
Chao Feng
[3]
Jinping Feng
journal
BMC cardiovascular disorders
year
2024
abstract
BACKGROUND: Acute myocardial injury, cytokine storms, hypoxemia and pathogen-mediated damage were the major causes responsible for mortality induced by coronavirus disease 2019 (COVID-19)-related myocarditis. These need ECMO treatment. We investigated differentially expressed genes (DEGs) in patients with COVID-19-related myocarditis and ECMO prognosis. METHODS: GSE150392 and GSE93101 were analyzed to identify DEGs. A Venn diagram was used to obtain the same transcripts between myocarditis-related and ECMO-related DEGs. Enrichment pathway analysis was performed and hub genes were identified. Pivotal miRNAs, transcription factors, and chemicals with the screened gene interactions were identified. The GSE167028 dataset and single-cell sequencing data were used to validate the screened genes. RESULTS: Using a Venn diagram, 229 overlapping DEGs were identified between myocarditis-related and ECMO-related DEGs, which were mainly involved in T cell activation, contractile actin filament bundle, actomyosin, cyclic nucleotide phosphodiesterase activity, and cytokine-cytokine receptor interaction. 15 hub genes and 15 neighboring DEGs were screened, which were mainly involved in the positive regulation of T cell activation, integrin complex, integrin binding, the PI3K-Akt signaling pathway, and the TNF signaling pathway. Data in GSE167028 and single-cell sequencing data were used to validate the screened genes, and this demonstrated that the screened genes CCL2, APOE, ITGB8, LAMC2, COL6A3 and TNC were mainly expressed in fibroblast cells; IL6, ITGA1, PTK2, ITGB5, IL15, LAMA4, CAV1, SNCA, BDNF, ACTA2, CD70, MYL9, DPP4, ENO2 and VEGFC were expressed in cardiomyocytes; IL6, PTK2, ITGB5, IL15, APOE, JUN, SNCA, CD83, DPP4 and ENO2 were expressed in macrophages; and IL6, ITGA1, PTK2, ITGB5, IL15, VCAM1, LAMA4, CAV1, ACTA2, MYL9, CD83, DPP4, ENO2, VEGFC and IL32 were expressed in vascular endothelial cells. CONCLUSION: The screened hub genes, IL6, ITGA1, PTK2, ITGB3, ITGB5, CCL2, IL15, VCAM1, GZMB, APOE, ITGB8, LAMA4, LAMC2, COL6A3 and TNFRSF9, were validated using GEO dataset and single-cell sequencing data, which may be therapeutic targets patients with myocarditis to prevent MI progression and adverse cardiovascular events.
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The study identified 229 overlapping differentially expressed genes between COVID-19-related myocarditis and ECMO prognosis-related DEGs.
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Using a Venn diagram, 229 overlapping DEGs were identified between myocarditis-related and ECMO-related DEGs, which were mainly involved in T cell activation, contractile actin filament bundle, actomyosin, cyclic nucleotide phosphodiesterase activity, and cytokine-cytokine receptor interaction.
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The study identified 229 overlapping differentially expressed genes between COVID-19-related myocarditis and ECMO prognosis-related DEGs.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39026189", "kind": "science-record", "revision": 4, "content_hash": "sha256:760b7db99fff9bbf5377b501f15fb6ff7cad3b3606fee46c8169f643a6c7449e", "created_at": "2026-11-01T20:29:06Z", "updated_at": "2026-11-01T22:54:43Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Coronavirus disease 2019-related myocarditis genes contribute to ECMO prognosis.", "doi": "10.1186/s12872-024-04032-5", "pmid": "39026189", "authors": ["An Yan", "Ruiying Zhang", "Chao Feng", "Jinping Feng"], "journal": "BMC cardiovascular disorders", "year": 2024, "abstract": "BACKGROUND: Acute myocardial injury, cytokine storms, hypoxemia and pathogen-mediated damage were the major causes responsible for mortality induced by coronavirus disease 2019 (COVID-19)-related myocarditis. These need ECMO treatment. We investigated differentially expressed genes (DEGs) in patients with COVID-19-related myocarditis and ECMO prognosis.\nMETHODS: GSE150392 and GSE93101 were analyzed to identify DEGs. A Venn diagram was used to obtain the same transcripts between myocarditis-related and ECMO-related DEGs. Enrichment pathway analysis was performed and hub genes were identified. Pivotal miRNAs, transcription factors, and chemicals with the screened gene interactions were identified. The GSE167028 dataset and single-cell sequencing data were used to validate the screened genes.\nRESULTS: Using a Venn diagram, 229 overlapping DEGs were identified between myocarditis-related and ECMO-related DEGs, which were mainly involved in T cell activation, contractile actin filament bundle, actomyosin, cyclic nucleotide phosphodiesterase activity, and cytokine-cytokine receptor interaction. 15 hub genes and 15 neighboring DEGs were screened, which were mainly involved in the positive regulation of T cell activation, integrin complex, integrin binding, the PI3K-Akt signaling pathway, and the TNF signaling pathway. Data in GSE167028 and single-cell sequencing data were used to validate the screened genes, and this demonstrated that the screened genes CCL2, APOE, ITGB8, LAMC2, COL6A3 and TNC were mainly expressed in fibroblast cells; IL6, ITGA1, PTK2, ITGB5, IL15, LAMA4, CAV1, SNCA, BDNF, ACTA2, CD70, MYL9, DPP4, ENO2 and VEGFC were expressed in cardiomyocytes; IL6, PTK2, ITGB5, IL15, APOE, JUN, SNCA, CD83, DPP4 and ENO2 were expressed in macrophages; and IL6, ITGA1, PTK2, ITGB5, IL15, VCAM1, LAMA4, CAV1, ACTA2, MYL9, CD83, DPP4, ENO2, VEGFC and IL32 were expressed in vascular endothelial cells.\nCONCLUSION: The screened hub genes, IL6, ITGA1, PTK2, ITGB3, ITGB5, CCL2, IL15, VCAM1, GZMB, APOE, ITGB8, LAMA4, LAMC2, COL6A3 and TNFRSF9, were validated using GEO dataset and single-cell sequencing data, which may be therapeutic targets patients with myocarditis to prevent MI progression and adverse cardiovascular events.", "claims": [{"id": "claim-method", "statement": "The data were analyzed using “DESeq2” (version 1.28.1) package in R.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39026189", "locator": "sections[3] \"Microarray data and data processing\" paragraph 4", "quote": "The data were analyzed using “DESeq2” (version 1.28.1) package in R."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Previously reported GEO data were used to support this study and are available at GSE150392, GSE93101 and GSE167028. These datasets are cited at relevant places within the text as references [13, 20, 21].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39026189", "locator": "sections[21] \"Data availability\" paragraph 2", "quote": "Previously reported GEO data were used to support this study and are available at GSE150392, GSE93101 and GSE167028. 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