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Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases - a proof of concept study.

Authors :
UCL - SSS/IREC/PEDI - Pôle de Pédiatrie
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service de pédiatrie
Ha, My Kieu
Bartholomeus, Esther
Van Os, Luc
Dandelooy, Julie
Leysen, Julie
Aerts, Olivier
Siozopoulou, Vasiliki
De Smet, Eline
Gielen, Jan
Guerti, Khadija
De Maeseneer, Michel
Herregods, Nele
Lechkar, Bouchra
Wittoek, Ruth
Geens, Elke
Claes, Laura
Zaqout, Mahmoud
Dewals, Wendy
Lemay, Annelies
Tuerlinckx, David
Weynants, David
Vanlede, Koen
van Berlaer, Gerlant
Raes, Marc
Verhelst, Helene
Boiy, Tine
Van Damme, Pierre
Jansen, Anna C
Meuwissen, Marije
Sabato, Vito
Van Camp, Guy
Suls, Arvid
Werff Ten Bosch, Jutte Van der
Dehoorne, Joke
Joos, Rik
Laukens, Kris
Meysman, Pieter
Ogunjimi, Benson
UCL - SSS/IREC/PEDI - Pôle de Pédiatrie
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service de pédiatrie
Ha, My Kieu
Bartholomeus, Esther
Van Os, Luc
Dandelooy, Julie
Leysen, Julie
Aerts, Olivier
Siozopoulou, Vasiliki
De Smet, Eline
Gielen, Jan
Guerti, Khadija
De Maeseneer, Michel
Herregods, Nele
Lechkar, Bouchra
Wittoek, Ruth
Geens, Elke
Claes, Laura
Zaqout, Mahmoud
Dewals, Wendy
Lemay, Annelies
Tuerlinckx, David
Weynants, David
Vanlede, Koen
van Berlaer, Gerlant
Raes, Marc
Verhelst, Helene
Boiy, Tine
Van Damme, Pierre
Jansen, Anna C
Meuwissen, Marije
Sabato, Vito
Van Camp, Guy
Suls, Arvid
Werff Ten Bosch, Jutte Van der
Dehoorne, Joke
Joos, Rik
Laukens, Kris
Meysman, Pieter
Ogunjimi, Benson
Source :
Pediatric rheumatology online journal, Vol. 20, no.1, p. 91 (2022)
Publication Year :
2022

Abstract

Transcriptome profiling of blood cells is an efficient tool to study the gene expression signatures of rheumatic diseases. This study aims to improve the early diagnosis of pediatric rheumatic diseases by investigating patients' blood gene expression and applying machine learning on the transcriptome data to develop predictive models. RNA sequencing was performed on whole blood collected from children with rheumatic diseases. Random Forest classification models were developed based on the transcriptome data of 48 rheumatic patients, 46 children with viral infection, and 35 controls to classify different disease groups. The performance of these classifiers was evaluated by leave-one-out cross-validation. Analyses of differentially expressed genes (DEG), gene ontology (GO), and interferon-stimulated gene (ISG) score were also conducted. Our first classifier could differentiate pediatric rheumatic patients from controls and infection cases with high area-under-the-curve (AUC) values (AUC = 0.8 ± 0.1 and 0.7 ± 0.1, respectively). Three other classifiers could distinguish chronic recurrent multifocal osteomyelitis (CRMO), juvenile idiopathic arthritis (JIA), and interferonopathies (IFN) from control and infection cases with AUC ≥ 0.8. DEG and GO analyses reveal that the pathophysiology of CRMO, IFN, and JIA involves innate immune responses including myeloid leukocyte and granulocyte activation, neutrophil activation and degranulation. IFN is specifically mediated by antibacterial and antifungal defense responses, CRMO by cellular response to cytokine, and JIA by cellular response to chemical stimulus. IFN patients particularly had the highest mean ISG score among all disease groups. Our data show that blood transcriptomics combined with machine learning is a promising diagnostic tool for pediatric rheumatic diseases and may assist physicians in making data-driven and patient-specific decisions in clinical practice.

Details

Database :
OAIster
Journal :
Pediatric rheumatology online journal, Vol. 20, no.1, p. 91 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372945421
Document Type :
Electronic Resource