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Plasma lipid profiles discriminate bacterial from viral infection in febrile children

  • EUCLIDS Consortium
  • Department of Infectious Disease, W2 1PG London, United Kingdom
  • National Phenome Centre and Imperial Clinical Phenotyping Centre, W12 0NN London, United Kingdom
  • Great North Children’s Hospital, NE1 4LP Newcastle upon Tyne, United Kingdom
  • Translational and Clinical Research Institute, NE2 4HH Newcastle upon Tyne, United Kingdom
  • NIHR Newcastle Biomedical Research Centre based at Newcastle upon Tyne Hospitals NHS Trust and Newcastle University, NE4 5PL Newcastle upon Tyne, United Kingdom
  • Department of Paediatric Emergency Medicine, W2 1NY London, United Kingdom
  • Institute of Infection and Global Health, L69 7BE Liverpool, United Kingdom
  • Department of Infectious Diseases, L12 2AP Liverpool, United Kingdom
  • Liverpool Health Partners, L3 5TF Liverpool, United Kingdom
  • Department of General Paediatrics, 8036 Graz, Austria
  • Pediatric Infectious Diseases and Immunology, 3508 AB Utrecht, Netherlands
  • Pediatric Infectious Diseases and Immunology, 6500 HB Nijmegen, Netherlands
  • Genetic, Galicia, Spain
  • Translational Pediatrics and Infectious Diseases, 15706 Galicia, Spain
  • Paediatirc Criticial Care Research Group, Brisbane, Australia
  • Department of Paediatrics, OX3 9DU Oxford, United Kingdom
  • Micropathology Ltd, CV4 7EZ Warwick, United Kingdom
  • Division of Pediatric Hematology, 1105 AZ Amsterdam, Netherlands
  • Medical Research Council Unit at the London School of Hygiene & Tropical Medicine, Banjul, Gambia
  • Vrije Universiteit University Medical Center, Amsterdam, Netherlands
  • University Medical Center Utrecht – Wilhelmina Children’s Hospital, Utrecht, Netherlands
  • Jeroen Bosch Hospital, ‘s-Hertogenbosch, Netherlands
  • Diakonessenhuis, Utrecht, Netherlands
  • Máxima Medical Center, Veldhoven, Netherlands.
  • Slingeland Hospital, Doetinchem, Netherlands
  • Catharina Hospital, Eindhoven, Netherlands
  • ETZ Elisabeth, Tilburg, Netherlands
  • Flevo hospital, Almere, Netherlands

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Fever is the most common reason that children present to Emergency Departments. Clinical signs and symptoms suggestive of bacterial infection are often non-specific, and there is no definitive test for the accurate diagnosis of infection. The ‘omics’ approaches to identifying biomarkers from the host-response to bacterial infection are promising. In this study, lipidomic analysis was carried out with plasma samples obtained from febrile children with confirmed bacterial infection (n = 20) and confirmed viral infection (n = 20). We show for the first time that bacterial and viral infection produces distinct profile in the host lipidome. Some species of glycerophosphoinositol, sphingomyelin, lysophosphatidylcholine and cholesterol sulfate were higher in the confirmed virus infected group, while some species of fatty acids, glycerophosphocholine, glycerophosphoserine, lactosylceramide and bilirubin were lower in the confirmed virus infected group when compared with confirmed bacterial infected group. A combination of three lipids achieved an area under the receiver operating characteristic (ROC) curve of 0.911 (95% CI 0.81 to 0.98). This pilot study demonstrates the potential of metabolic biomarkers to assist clinicians in distinguishing bacterial from viral infection in febrile children, to facilitate effective clinical management and to the limit inappropriate use of antibiotics.
Original languageEnglish
Article number17714
JournalScientific reports
Volume9
Issue number1
DOIs
Publication statusPublished - 1 Dec 2019

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