Plasma lipid profiles discriminate bacterial from viral infection in febrile children

被引:0
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作者
Xinzhu Wang
Ruud Nijman
Stephane Camuzeaux
Caroline Sands
Heather Jackson
Myrsini Kaforou
Marieke Emonts
Jethro A. Herberg
Ian Maconochie
Enitan D. Carrol
Stephane C. Paulus
Werner Zenz
Michiel Van der Flier
Ronald de Groot
Federico Martinon-Torres
Luregn J. Schlapbach
Andrew J. Pollard
Colin Fink
Taco T. Kuijpers
Suzanne Anderson
Matthew R. Lewis
Michael Levin
Myra McClure
机构
[1] Imperial College London,Department of Infectious Disease
[2] National Phenome Centre and Imperial Clinical Phenotyping Centre,Translational and Clinical Research Institute
[3] Department of Metabolism,Department of Paediatric Emergency Medicine
[4] Digestion and Reproduction,Department of Infectious Diseases
[5] IRDB Building,Department of General Paediatrics
[6] Great North Children’s Hospital,Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital
[7] Paediatric Immunology,Pediatric Infectious Diseases and Immunology, Amalia Children’s Hospital, and Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Department of Laboratory Medicine, Radboud Institute for Molecular Life Sciences
[8] Infectious Diseases & Allergy,Genetic, Vaccines and Pediatric Infectious Diseases Research Group (GENVIP)
[9] Newcastle upon Tyne Hospitals NHS Foundation Trust,Translational Pediatrics and Infectious Diseases, Department of Pediatrics
[10] Newcastle University,Paediatirc Criticial Care Research Group, Child Health Research Centre
[11] NIHR Newcastle Biomedical Research Centre based at Newcastle upon Tyne Hospitals NHS Trust and Newcastle University,Department of Paediatrics
[12] St Mary’s Hospital,Micropathology Ltd
[13] Imperial College NHS Healthcare Trust,Division of Pediatric Hematology
[14] Institute of Infection and Global Health,Department of Pediatrics
[15] University of Liverpool,Service of Neonatology
[16] Alder Hey Children’s NHS Foundation Trust,Infectious Diseases Service
[17] Liverpool Health Partners,Department of Pediatrics
[18] Medical University of Graz,Pediatric Infectious Diseases Unit, Children’s Hospital of Geneva
[19] Graz,Infectious Diseases and Vaccinology
[20] Auenbruggerplatz 34/2,Department of Neonatology
[21] University Medical Center Utrecht,Department of Pediatric and Adolescence Surgery
[22] Radboud University Medical Center,Department of Pediatrics
[23] Instituto de Investigación Sanitaria de Santiago and Universidad de Santiago de Compostela (USC),Department of Pediatrics/Department of Pediatric Surgery
[24] Hospital Clínico Universitario de Santiago de Compostela,Department of Pediatrics
[25] The University of Queensland and Paediatric Intensive Care Research Group,Department of Pediatrics
[26] Queensland Children’s Hospital,Department of Pediatrics
[27] University of Oxford and the NIHR Oxford Biomedical Research Centre,Department of Pulmonology
[28] University of Warwick,Institute for Hygiene and Microbiology
[29] Immunology and Infectious diseases,Clinical Institute of Medical and Chemical Laboratory Diagnostics
[30] Emma Children’s Hospital Academic Medical Center,Department of Pediatric Orthopedics and Adult Foot and Ankle Surgery
[31] Medical Research Council Unit at the London School of Hygiene & Tropical Medicine,Department of Paediatrics
[32] Poole Hospital NHS Foundation Trust,Department of Pediatrics and Adolescent Medicine
[33] Cambridge University Hospitals NHS Trust,Department of Neonatology and Paediatric Intensive Care
[34] University Hospital Southampton,Department of Pediatrics
[35] Nottingham University Hospital NHS Trust,Department of Pediatrics and Adolescent Medicine
[36] University Hospitals of Leicester NHS Trust,Department of General Paediatrics
[37] Portsmouth Hospitals NHS Trust,Department of Paediatrics
[38] Great Ormond Street Hospital,Department of Paediatrics and Adolescents Medicine
[39] King’s College Hospital NHS Foundation Trust,Department of Pediatrics and Adolescent Medicine
[40] Oxford University Hospitals NHS Foundation Trust,Paediatric Intensive Care Unit
[41] Kettering General Hospital NHS Foundation Trust,Department of Pediatric and Adolescence Surgery, Division of Pediatric Orthopedics
[42] Central Manchester NHS Trust,Department of Pediatrics
[43] Unidade de Xenética,University Children’s Hospital
[44] Departamento de Anatomía Patolóxica e Ciencias Forenses,Department of Pediatric Surgery
[45] Instituto de Ciencias Forenses,Department of Paediatrics
[46] Facultade de Medicina,Children’s Hospital
[47] Universidade de Santiago de Compostela,undefined
[48] and GenPop Research Group,undefined
[49] Instituto de Investigaciones Sanitarias (IDIS),undefined
[50] Hospital Clínico Universitario de Santiago,undefined
来源
Scientific Reports | / 9卷
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摘要
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.
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