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Kawasaki Disease Patient Stratification and Pathway Analysis Based on Host Transcriptomic and Proteomic Profiles.
Jackson, Heather; Menikou, Stephanie; Hamilton, Shea; McArdle, Andrew; Shimizu, Chisato; Galassini, Rachel; Huang, Honglei; Kim, Jihoon; Tremoulet, Adriana; Thorne, Adam; Fischer, Roman; de Jonge, Marien I; Kuijpers, Taco; Wright, Victoria; Burns, Jane C; Casals-Pascual, Climent; Herberg, Jethro; Levin, Mike; Kaforou, Myrsini.
Afiliación
  • Jackson H; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Menikou S; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Hamilton S; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • McArdle A; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Shimizu C; Department of Pediatrics, University of California San Diego, La Jolla, CA 92093, USA.
  • Galassini R; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Huang H; Target Discovery Institute, University of Oxford, Oxford OX3 7FZ, UK.
  • Kim J; Department of Biomedical Informatics, University of California San Diego, La Jolla, CA 92093, USA.
  • Tremoulet A; Department of Pediatrics, University of California San Diego, La Jolla, CA 92093, USA.
  • Thorne A; Department of Surgery, Section of Hepatobiliary Surgery and Liver Transplantation, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
  • Fischer R; Discovery Proteomics Facility, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford OX3 9DU, UK.
  • de Jonge MI; Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • Kuijpers T; Department of Pediatric Immunology, Rheumatology, and Infectious Diseases, Emma Children's Hospital, Amsterdam University Medical Center (AMC), 1105 AZ Amsterdam, The Netherlands.
  • Wright V; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Burns JC; Department of Pediatrics, University of California San Diego, La Jolla, CA 92093, USA.
  • Casals-Pascual C; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
  • Herberg J; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Levin M; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
  • Kaforou M; Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
Int J Mol Sci ; 22(11)2021 May 26.
Article en En | MEDLINE | ID: mdl-34073389
ABSTRACT
The aetiology of Kawasaki disease (KD), an acute inflammatory disorder of childhood, remains unknown despite various triggers of KD having been proposed. Host 'omic profiles offer insights into the host response to infection and inflammation, with the interrogation of multiple 'omic levels in parallel providing a more comprehensive picture. We used differential abundance analysis, pathway analysis, clustering, and classification techniques to explore whether the host response in KD is more similar to the response to bacterial or viral infections at the transcriptomic and proteomic levels through comparison of 'omic profiles from children with KD to those with bacterial and viral infections. Pathways activated in patients with KD included those involved in anti-viral and anti-bacterial responses. Unsupervised clustering showed that the majority of KD patients clustered with bacterial patients on both 'omic levels, whilst application of diagnostic signatures specific for bacterial and viral infections revealed that many transcriptomic KD samples had low probabilities of having bacterial or viral infections, suggesting that KD may be triggered by a different process not typical of either common bacterial or viral infections. Clustering based on the transcriptomic and proteomic responses during KD revealed three clusters of KD patients on both 'omic levels, suggesting heterogeneity within the inflammatory response during KD. The observed heterogeneity may reflect differences in the host response to a common trigger, or variation dependent on different triggers of the condition.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Bacterianas / Virosis / Perfilación de la Expresión Génica / Proteómica / Síndrome Mucocutáneo Linfonodular Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Bacterianas / Virosis / Perfilación de la Expresión Génica / Proteómica / Síndrome Mucocutáneo Linfonodular Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido