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February 27, 2026Clinical and Experimental Pediatrics0 citationsOpen Access

Multiomics approaches in Kawasaki disease: insights into pathogenesis and emerging directions for diagnosis and treatment

JAJong Gyun AhnIKInsoo Kang

Key Points

  • This research aims to explore the mechanisms underlying Kawasaki disease and improve diagnostic and treatment options.
  • Utilized high-throughput technologies including genomics, proteomics, and metabolomics.
  • Integrated multiomics profiles to identify key inflammatory and vascular pathways.
  • Prioritized pathways for future biomarker discovery and clinical application.
  • Identified several convergent mechanistic axes linked to systemic inflammation and coronary artery lesions.
  • Established a framework for potential biomarkers and therapeutic hypotheses related to Kawasaki disease.
  • Emphasized the need for prospective validation and standardization of diagnostic assays.

Abstract

Kawasaki disease (KD) is an acute febrile vasculitis and the leading cause of acquired heart disease in children. Despite decades of research, the etiology remains unknown and key mechanisms linking systemic inflammation to coronary artery lesions are incompletely defined. High-throughput technologies-including genomics, transcriptomics, proteomics, metabolomics, epigenomics, and immunomics-have enabled systems-level profiling of KD and highlighted reproducible inflammatory and vascular pathways. Multiomics integration increasingly supports convergent mechanistic axes, particularly interleukin (IL-1/IL-6-neutrophil programs, Fcγ-receptor signaling related to intravenous immunoglobulin (IVIG) pharmacodynamics, Ca²+/nuclear factor of activated T cells-dependent T-cell activation, and endothelial/extracellular matrix remodeling associated with coronary outcomes. While these findings provide a robust framework for biomarker discovery and therapeutic hypothesis generation, most signatures remain investigational and require prospective validation, standardized sampling (pre-/post-IVIG), and clinically scalable assays before routine implementation. This review summarizes current multiomics applications in KD, prioritizes the most consistently supported pathways, and outlines a pragmatic roadmap toward clinically useful risk stratification, disease monitoring, and outcome prediction.

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Cite This Study

Ahn et al. (2026) studied this question.

synapsesocial.com/papers/69a134fbed1d949a99abe6a4https://doi.org/10.3345/cep.2025.02901
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Metagenomic analysis demonstrates distinct changes in the gut microbiome of Kawasaki diseases children2024 · 9 citations
  2. 2Polymorphism-driven immune disruptions in Kawasaki disease across populations: decoding the role of T and B-cells2025 · 3 citations
  3. 3Identification and mechanistic elucidation of neutrophil migration-related biomarkers in Kawasaki disease based on single-cell and transcriptome sequencing2026
  4. 4MicroRNAs in Kawasaki disease: An update on diagnosis, therapy and monitoring2022 · 28 citations
  5. 5Knowledge graph visualization and bibliometric analysis of research on coronary artery lesions in Kawasaki disease2026