Evidence map›Paper›PMID 31776453›Full record

ArticleScientific reports2019

Plasma lipid profiles discriminate bacterial from viral infection in febrile children.

Xinzhu Wang, Ruud Nijman, Stephane Camuzeaux, Caroline Sands, Heather Jackson, Myrsini Kaforou, Marieke Emonts, Jethro A Herberg, Ian Maconochie, Enitan D Carrol and 14 more

Registry-linked trialAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01022268 (A Comprehensive, Long-term Integrated Programme to Study the Aetiology and Immunopathology of Childhood Infectious, Inflammatory and Allergic Disease, Using the Large Patient Base of Children Attending St Mary's Hospital, London), which is not on this map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01022268 completednot on this map

A Comprehensive, Long-term Integrated Programme to Study the Aetiology and Immunopathology of Childhood Infectious, Inflammatory and Allergic Disease, Using the Large Patient Base of Children Attending St Mary's Hospital, London

TypeobservationalSponsorImperial College LondonRan2009 to 2019Enrolled902ConditionsInfection, Inflammation, Allergy, Children
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Clinical lipidomics in bacterial sepsis: a systematic review of serum and plasma evaluations.Metabolomics : Official journal of the Metabolomic Society · 2026
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Plasma Metabolomics Reveals Distinct Biological and Diagnostic Signatures for Melioidosis.American journal of respiratory and critical care medicine · 2024
    Article
  8. The Implication of Sphingolipids in Viral Infections.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Xinzhu WangDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom.
Ruud NijmanDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom.
Stephane CamuzeauxNational Phenome Centre and Imperial Clinical Phenotyping Centre, Department of Metabolism, Digestion and Reproduction, IRDB Building, Du Cane Road, Imperial College London, London, W12 0NN, United Kingdom.
Caroline SandsNational Phenome Centre and Imperial Clinical Phenotyping Centre, Department of Metabolism, Digestion and Reproduction, IRDB Building, Du Cane Road, Imperial College London, London, W12 0NN, United Kingdom.ORCID http://orcid.org/0000-0002-3749-7941
Heather JacksonDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom.ORCID http://orcid.org/0000-0002-1054-9983
Myrsini KaforouDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom.ORCID http://orcid.org/0000-0001-9878-4007
Marieke EmontsGreat North Children's Hospital, Paediatric Immunology, Infectious Diseases & Allergy, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, NE1 4LP, United Kingdom.
Jethro A HerbergDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom.
Ian MaconochieDepartment of Paediatric Emergency Medicine, St Mary's Hospital, Imperial College NHS Healthcare Trust, London, W2 1NY, United Kingdom.
Enitan D CarrolInstitute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, United Kingdom.
Stephane C PaulusDepartment of Infectious Diseases, Alder Hey Children's NHS Foundation Trust, Liverpool, L12 2AP, United Kingdom.ORCID http://orcid.org/0000-0002-0703-9114
Werner ZenzDepartment of General Paediatrics, Medical University of Graz, Graz, Auenbruggerplatz 34/2, 8036, Graz, Austria.
Michiel Van der FlierPediatric Infectious Diseases and Immunology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, 3508 AB, The Netherlands.
Ronald de GrootPediatric 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, Radboud University Medical Center, Nijmegen, 6500 HB, The Netherlands.
Federico Martinon-TorresGenetic, Vaccines and Pediatric Infectious Diseases Research Group (GENVIP), Instituto de Investigación Sanitaria de Santiago and Universidad de Santiago de Compostela (USC), Galicia, Spain.ORCID http://orcid.org/0000-0002-9023-581X
Luregn J SchlapbachPaediatirc Criticial Care Research Group, Child Health Research Centre, The University of Queensland and Paediatric Intensive Care Research Group, Queensland Children's Hospital, Brisbane, Australia.
Andrew J PollardDepartment of Paediatrics, University of Oxford and the NIHR Oxford Biomedical Research Centre, Oxford, OX3 9DU, United Kingdom.
Colin FinkMicropathology Ltd, University of Warwick, Warwick, CV4 7EZ, United Kingdom.
Taco T KuijpersDivision of Pediatric Hematology, Immunology and Infectious diseases, Emma Children's Hospital Academic Medical Center, Amsterdam, 1105 AZ, The Netherlands.
Suzanne AndersonMedical Research Council Unit at the London School of Hygiene & Tropical Medicine, Banjul, The Gambia.
Matthew R LewisNational Phenome Centre and Imperial Clinical Phenotyping Centre, Department of Metabolism, Digestion and Reproduction, IRDB Building, Du Cane Road, Imperial College London, London, W12 0NN, United Kingdom.
Michael LevinDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom.
Myra McClureDepartment of Infectious Disease, Imperial College London, London, W2 1PG, United Kingdom. m.mcclure@imperial.ac.uk.
EUCLIDS consortium

Funding

Medical Research Council MC_PC_12025MRF_ C0483Wellcome TrustWellcome Trust 206508/Z/17/ZWellcome Trust MC_PC_12025
6 · The paper itself

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.

Indexed as

AdolescentBacterial InfectionsBiomarkersChildChild, PreschoolCholesterolDiagnosis, DifferentialFemaleFever of Unknown OriginHumansInfantInositol PhosphatesLysophosphatidylcholinesMaleSphingomyelinsVirus DiseasesBiomarkersCholesterolglycerylphosphoinositolInositol PhosphatesLysophosphatidylcholinesSphingomyelins

Identifiers

PMID31776453
PMCPMC6881435

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.