Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis

Background: Myasthenia gravis (MG) and idiopathic inflammatory myopathies (IIM) are autoimmune disorders that can co-occur, complicating diagnosis and treatment. The molecular mechanisms underlying this comorbidity are not well understood. Objective: This study aims to identify common differentially...

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Main Authors: Wenqu Yang, Feng Liang
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Heliyon
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Online Access:http://www.sciencedirect.com/science/article/pii/S2405844024174737
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author Wenqu Yang
Feng Liang
author_facet Wenqu Yang
Feng Liang
author_sort Wenqu Yang
collection DOAJ
description Background: Myasthenia gravis (MG) and idiopathic inflammatory myopathies (IIM) are autoimmune disorders that can co-occur, complicating diagnosis and treatment. The molecular mechanisms underlying this comorbidity are not well understood. Objective: This study aims to identify common differentially expressed genes (co-DEGs) between MG and IIM to elucidate shared pathogenic pathways and potential therapeutic targets. Methods: Transcriptomic data from the Gene Expression Omnibus (GEO) were analyzed using the ''limma'' package in RStudio. Functional enrichment analyses were performed using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. A nomogram prediction model was developed, and receiver operating characteristic (ROC) analysis was used to evaluate its diagnostic potential. Results: Four co-DEGs were identified between MG and IIM, associated with neurotransmitter transport and ion channel regulation. The nomogram model, incorporating three of these co-DEGs, showed high predictive accuracy for MG with IIM complications, with an area under the ROC curve of 0.94. Immune infiltration analysis revealed distinct patterns in MG and IIM, particularly involving gamma delta T cells and activated mast cells. Conclusion: The study identifies key genetic intersections between MG and IIM, providing insights into their shared pathogenesis and highlighting potential diagnostic and therapeutic targets. Further experimental validation is required to confirm these findings.
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spelling doaj-art-1f5dc2f347bf4b339795d2d048f61d712025-01-17T04:51:17ZengElsevierHeliyon2405-84402025-01-01111e41442Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesisWenqu Yang0Feng Liang1Department of Anesthesiology, Shanxi Bethune Hospital, China; Corresponding author. No.99, Longcheng Street, Taiyuan, Shanxi, China.Department of Neurology, The First Hospital of Tsinghua University, China; Shanxi Medical University, ChinaBackground: Myasthenia gravis (MG) and idiopathic inflammatory myopathies (IIM) are autoimmune disorders that can co-occur, complicating diagnosis and treatment. The molecular mechanisms underlying this comorbidity are not well understood. Objective: This study aims to identify common differentially expressed genes (co-DEGs) between MG and IIM to elucidate shared pathogenic pathways and potential therapeutic targets. Methods: Transcriptomic data from the Gene Expression Omnibus (GEO) were analyzed using the ''limma'' package in RStudio. Functional enrichment analyses were performed using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. A nomogram prediction model was developed, and receiver operating characteristic (ROC) analysis was used to evaluate its diagnostic potential. Results: Four co-DEGs were identified between MG and IIM, associated with neurotransmitter transport and ion channel regulation. The nomogram model, incorporating three of these co-DEGs, showed high predictive accuracy for MG with IIM complications, with an area under the ROC curve of 0.94. Immune infiltration analysis revealed distinct patterns in MG and IIM, particularly involving gamma delta T cells and activated mast cells. Conclusion: The study identifies key genetic intersections between MG and IIM, providing insights into their shared pathogenesis and highlighting potential diagnostic and therapeutic targets. Further experimental validation is required to confirm these findings.http://www.sciencedirect.com/science/article/pii/S2405844024174737Myasthenia gravisIdiopathic inflammatory myopathiesCommon differentially expressed genesSmall molecular compounds
spellingShingle Wenqu Yang
Feng Liang
Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
Heliyon
Myasthenia gravis
Idiopathic inflammatory myopathies
Common differentially expressed genes
Small molecular compounds
title Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
title_full Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
title_fullStr Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
title_full_unstemmed Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
title_short Elucidating genetic intersections: Co-differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
title_sort elucidating genetic intersections co differentially expressed genes in myasthenia gravis and idiopathic inflammatory myopathies and their role in comorbid pathogenesis
topic Myasthenia gravis
Idiopathic inflammatory myopathies
Common differentially expressed genes
Small molecular compounds
url http://www.sciencedirect.com/science/article/pii/S2405844024174737
work_keys_str_mv AT wenquyang elucidatinggeneticintersectionscodifferentiallyexpressedgenesinmyastheniagravisandidiopathicinflammatorymyopathiesandtheirroleincomorbidpathogenesis
AT fengliang elucidatinggeneticintersectionscodifferentiallyexpressedgenesinmyastheniagravisandidiopathicinflammatorymyopathiesandtheirroleincomorbidpathogenesis