Skip to main navigation Skip to search Skip to main content

A dual covari-ant biomarker approach to Kawasaki disease, using vascular endothelial growth factor A and B gene expression; implications for coronary pathogenesis

  • Asrar Rashid*
  • , Govind Benakatti
  • , Feras Al-Obeidat
  • , Rajesh Phatak
  • , Zainab A. Malik
  • , Javed Sharief
  • , Raziya Kadwa
  • , Wael Hafez
  • , Mohammed Toufiq
  • , Damien Chaussabel
  • , Rayaz Malik
  • , Nasir Quraishi
  • , Syed Ahmed Zaki
  • , Guftar Shaikh
  • , Amir Hussain
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Kawasaki disease (KD) is the most common vasculitis in young children, with coronary artery lesions (CALs) and coronary aneurysms (CAAs) being responsible for most KD-related deaths. Objective: We hypothesized that Vascular Endothelial Growth Factors (VEGFs) are pivotal in KD inflammation and coronary artery lesions. This study assessed VEGF-A and VEGF-B gene expression (GE) as potential biomarkers in KD inflammation. Study design: We analyzed NCBI-GEO datasets, categorizing gene expression patterns as “inflammatory” or "non-inflammatory". We focused on TNF-, NFKB1, VEGF-A, and VEGF-B GEs. Datasets were filtered based on differential changes in TNF and NFKB1 levels to isolate those with inflammatory shifts. Results: Inflammatory datasets (GSE63881, GSE73464, and GSE68004) displayed elevated TNF, NFKB1, and VEGF-A GE levels during acute KD. VEGF-B GE exhibited a distinctive trend: an initial drop and subsequent rise during recovery, a pattern that was missing in the non-inflammatory group. The treatment response was also studied, with intravenous immunoglobulin (IVIG) responders showing significant downregulation of NFKB1 GE after treatment: GSE16797 [IVIG ± methylprednisolone; p = 8.6443-03], GSE48498 [IVIG; p = 6.618e-02, infliximab; p = 3.240e-03], and GSE18606 [IVIG; p = 3.518e-02]. Considering the similar binding of VEGF-A and VEGF-B to the VEGFR1 receptor, a co-variate and inverse relationship is suggested. Conclusion: Temporal VEGF-A, VEGF-B, and GE changes show promise as new post-inflammatory biomarkers for KD. Novelty results with the biomarker approach, with the potential for a dual temporal relationship between VEGF-A and VEGF-A. A comprehensive exploration of VEGF-A and VEGF-B genes and protein analysis in KD is warranted to understand the functional aspects of these changes and how best to utilize the pattern of changes for therapeutic benefit.

Original languageEnglish
Article number101384
JournalInformatics in Medicine Unlocked
Volume43
DOIs
StatePublished - Jan 2023
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Gene-expression
  • Kawasaki disease
  • NFKB1
  • TNF
  • Temporal
  • VEGF-A
  • VEGF-B

ASJC Scopus subject areas

  • Software
  • General Computer Science
  • Information Systems
  • Health Informatics
  • Computer Science Applications

Fingerprint

Dive into the research topics of 'A dual covari-ant biomarker approach to Kawasaki disease, using vascular endothelial growth factor A and B gene expression; implications for coronary pathogenesis'. Together they form a unique fingerprint.

Cite this