Vasculitis & polymyalgia rheumatica

Neutrophil extracellular traps-associated candidate genes in IgA vasculitis: an exploratory multi-omics analysis integrating transcriptomics and Mendelian randomization

Pediatr Rheumatol Online JPublished Mechanistic study

Authors' conclusion

This exploratory multi-omics study identified a set of NET-associated candidate genes showing consistent associations with IgAV.

Study context

Population
IgA vasculitis (IgAV) patients and healthy controls; peripheral-blood bulk transcriptomic data
Comparison
IgAV patients vs healthy controls
Outcome
NET-associated candidate genes related to IgAV
Methodological detailsexploratory, multi-omics, transcriptomics, two-sample Mendelian randomization, cell-type-specific Mendelian randomization (MR), single-cell RNA sequencing (scRNA-seq), 646 NET-associated genes evaluated with gene set enrichment analysis (GSEA) and gene set variation analysis (GSVA); DEGs, GSEA leading-edge genes and transcriptome-wide association study (TWAS)-significant genes intersected
  • Exploratory
  • Multi-omics
  • Transcriptomics
  • Two-sample Mendelian randomization
  • Cell-type-specific MR
  • scRNA-seq
  • 646 NET-associated genes evaluated with GSEA and GSVA; DEGs, GSEA leading-edge genes and TWAS-significant genes intersected

Main finding

As reported in the abstract

NET-associated candidate genes
Five NET-associated candidate genes (AGER, TLR2, CXCR2, TEK, THBD) consistently prioritized across analyses
5

Further findings

Single-cell expression

Genes mainly expressed in myeloid immune subsets, with elevated NETosis-related transcriptional signatures

Intercellular communication

Enhanced activity of immune-related signalling pathways, incl. MHC-I and MIF, in IgAV samples

Original publication

Neutrophil extracellular traps-associated candidate genes in IgA vasculitis: an exploratory multi-omics analysis integrating transcriptomics and Mendelian randomization. Pediatr Rheumatol Online J. Published 5 March 2026. doi:10.1186/s12969-026-01197-5

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