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Transcriptomic analysis reveals the potential crosstalk genes and immune relationship between Crohn's disease and
Xiaohan Qiu1,2, Junlin Teng1,2, Ning Wang1,2
1National Key Laboratory for Innovation and Transformation of Luobing Theory, the Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education, Chinese National Health Commission and Chinese Academy of Medical Sciences, Jinan, China.
This study identified shared genes CXCL16 and HLA-DPB1 between Crohn's disease (CD) and atrial fibrillation (AF). Findings suggest immune cells like T cells and dendritic cells play a role in both conditions.
Area of Science:
- Genetics and Immunology
- Cardiovascular Research
- Gastroenterology
Background:
- Crohn's disease (CD) and atrial fibrillation (AF) share inflammatory and autoimmune characteristics.
- Emerging evidence suggests an elevated risk of AF in individuals with CD.
- Limited research exists on the shared genetic and immunological underpinnings of CD and AF.
Purpose of the Study:
- To investigate shared genes, pathways, and immune cell infiltration between CD and AF.
- To identify potential molecular links connecting these two distinct conditions.
- To explore the immunological basis for the observed association between CD and AF.
Main Methods:
- Utilized weighted gene co-expression network analysis (WGCNA) to identify shared genes from GEO datasets.
- Performed Gene Ontology (GO) and KEGG pathway enrichment analyses on key gene modules.
- Applied LASSO regression and SVM for hub gene screening, followed by ssGSEA for immune cell infiltration analysis.
Main Results:
- Identified 30 shared genes associated with the pathology of both AF and CD using WGCNA.
- GO analysis revealed enrichment in pathways related to major histocompatibility complex (MHC) and antigen processing.
- Pinpointed CXCL16 and HLA-DPB1 as key overlapping genes; observed increased CD4+, CD8+ T cells, and dendritic cells.
Conclusions:
- Identified CXCL16 and HLA-DPB1 as significant genes linking CD and AF through bioinformatics analysis.
- Suggests a crucial role for immune responses involving CD4+, CD8+ T cells, and dendritic cells in the interplay between CD and AF.
- Provides a genetic and immunological basis for understanding the co-occurrence of CD and AF.
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