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pmid:35901050

Gene module regulation in dilated cardiomyopathy and the role of Na/K-ATPase.

Yingnyu Gao · Lilian N D Silva · John D Hurley · Xiaoming Fan · Sandrine V Pierre · Komal Sodhi · Jiang Liu · Joseph I Shapiro · Jiang Tian

PloS one · 2022 doi:10.1371/journal.pone.0272117

Paper

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Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35901050
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title
Gene module regulation in dilated cardiomyopathy and the role of Na/K-ATPase.
doi
10.1371/journal.pone.0272117
pmid
35901050
authors array · 9 items
[0]
Yingnyu Gao
[1]
Lilian N D Silva
[2]
John D Hurley
[3]
Xiaoming Fan
[4]
Sandrine V Pierre
[5]
Komal Sodhi
[6]
Jiang Liu
[7]
Joseph I Shapiro
[8]
Jiang Tian
journal
PloS one
year
2022
abstract
Dilated cardiomyopathy (DCM) is a major cause of cardiac death and heart transplantation. It has been known that black people have a higher incidence of heart failure and related diseases compared to white people. To identify the relationship between gene expression and cardiac function in DCM patients, we performed pathway analysis and weighted gene co-expression network analysis (WGCNA) using RNA-sequencing data (GSE141910) from the NCBI Gene Expression Omnibus (GEO) database and identified several gene modules that were significantly associated with the left ventricle ejection fraction (LVEF) and DCM phenotype. Genes included in these modules are enriched in three major categories of signaling pathways: fibrosis-related, small molecule transporting-related, and immune response-related. Through consensus analysis, we found that gene modules associated with LVEF in African Americans are almost identical as in Caucasians, suggesting that the two groups may have more common rather than disparate genetic regulations in the etiology of DCM. In addition to the identified modules, we found that the gene expression level of Na/K-ATPase, an important membrane ion transporter, has a strong correlation with the LVEF. These clinical results are consistent with our previous findings and suggest the clinical significance of Na/K-ATPase regulation in DCM.
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We performed the gene expression analysis using DESeq2 based on the published RNA-sequencing data obtained from the GEO141910 cohort.
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sections[12] "Gene expression and pathway changes in DCM patients receiving heart transplants compared to non-failing donors" paragraph 2
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We performed the gene expression analysis using DESeq2 based on the published RNA-sequencing data obtained from the GEO141910 cohort.
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The relevant data for this study are publicly available from the NCBI GEO database (GSE141910; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE141910). The clinical phenotype data and gene expression count data of this cohort are publicly available online from the Github database (https://github.com/mpmorley/MAGNet).
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The relevant data for this study are publicly available from the NCBI GEO database (GSE141910; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE141910). The clinical phenotype data and gene expression count data of this cohort are publicly available online from the Github database (https://github.com/mpmorley/MAGNet).
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The comparison of eigengene and group module characteristics showed an overall similarity of 0.94 between African American and Caucasian American groups.
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The comparison of eigengene and group module characteristics showed an overall similarity of 0.94 (Fig 5B).
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The comparison of eigengene and group module characteristics showed an overall similarity of 0.94 between African American and Caucasian American groups.
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co-expression network analysis (WGCNA) using RNA-sequencing data (GSE141910) from the NCBI Gene Expressi
[1]
kilobase of exon per million reads) data of RNA-sequencing were downloaded from public available NCBI G
[2]
ristics of patients and donors The published RNA-sequencing dataset (GEO141910) is a cohort of heart fai
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non-failing donors. The data also contained RNA-sequencing data of 28 hypertrophic cardiomyopathy (HCM)
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Na/K-ATPase α1 reduction caused cardiac cell apoptosis and tissue fibrosis and was closely related
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other kinases were downregulated, while cell apoptosis-related genes such as Casp9 were upregulated
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We performed the gene expression analysis using DESeq2 based on the published RNA-sequencing data obtained from the GEO141910 cohort.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35901050", "kind": "science-record", "revision": 5, "content_hash": "sha256:9624bcef4846f7919ec91ba43c99f8e2c455bb2fc3d72442709aaa84270f52c6", "created_at": "2026-11-01T18:14:59Z", "updated_at": "2026-11-01T22:49:40Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Gene module regulation in dilated cardiomyopathy and the role of Na/K-ATPase.", "doi": "10.1371/journal.pone.0272117", "pmid": "35901050", "authors": ["Yingnyu Gao", "Lilian N D Silva", "John D Hurley", "Xiaoming Fan", "Sandrine V Pierre", "Komal Sodhi", "Jiang Liu", "Joseph I Shapiro", "Jiang Tian"], "journal": "PloS one", "year": 2022, "abstract": "Dilated cardiomyopathy (DCM) is a major cause of cardiac death and heart transplantation. It has been known that black people have a higher incidence of heart failure and related diseases compared to white people. To identify the relationship between gene expression and cardiac function in DCM patients, we performed pathway analysis and weighted gene co-expression network analysis (WGCNA) using RNA-sequencing data (GSE141910) from the NCBI Gene Expression Omnibus (GEO) database and identified several gene modules that were significantly associated with the left ventricle ejection fraction (LVEF) and DCM phenotype. Genes included in these modules are enriched in three major categories of signaling pathways: fibrosis-related, small molecule transporting-related, and immune response-related. Through consensus analysis, we found that gene modules associated with LVEF in African Americans are almost identical as in Caucasians, suggesting that the two groups may have more common rather than disparate genetic regulations in the etiology of DCM. In addition to the identified modules, we found that the gene expression level of Na/K-ATPase, an important membrane ion transporter, has a strong correlation with the LVEF. 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The data also contained RNA-sequencing data of 28 hypertrophic cardiomyopathy (HCM)"], "order_basis": "paper_text_order:431", "id": "assay:1"}, {"role": "data_generation", "definition_id": "apoptosis_assay", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["Na/K-ATPase α1 reduction caused cardiac cell apoptosis and tissue fibrosis and was closely related", "other kinases were downregulated, while cell apoptosis-related genes such as Casp9 were upregulated"], "order_basis": "paper_text_order:6104", "id": "assay:2"}, {"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["We performed the gene expression analysis using DESeq2 based on the published RNA-sequencing data obtained from the GEO141910 cohort."], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}