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Characterisation of paediatric brain tumours by their MRS metabolite profiles.
Gill, Simrandip K; Rose, Heather E L; Wilson, Martin; Rodriguez Gutierrez, Daniel; Worthington, Lara; Davies, Nigel P; MacPherson, Lesley; Hargrave, Darren R; Saunders, Dawn E; Clark, Christopher A; Payne, Geoffrey S; Leach, Martin O; Howe, Franklyn A; Auer, Dorothee P; Jaspan, Tim; Morgan, Paul S; Grundy, Richard G; Avula, Shivaram; Pizer, Barry; Arvanitis, Theodoros N; Peet, Andrew C.
Afiliação
  • Gill SK; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Rose HEL; Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Wilson M; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Rodriguez Gutierrez D; Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Worthington L; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Davies NP; Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • MacPherson L; Medical Physics, Nottingham University Hospital, Queen's Medical Centre, Nottingham, UK.
  • Hargrave DR; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Saunders DE; Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Clark CA; Department of Imaging and Medical Physics, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Payne GS; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Leach MO; Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Howe FA; Department of Imaging and Medical Physics, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Auer DP; Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Jaspan T; Paediatric Oncology Unit, Great Ormond Street Hospital For Sick Children, London, UK.
  • Morgan PS; Paediatric Oncology Unit, Great Ormond Street Hospital For Sick Children, London, UK.
  • Grundy RG; Developmental Imaging and Biophysics Section, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Avula S; CRUK Cancer Imaging Centre, The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London, UK.
  • Pizer B; CRUK Cancer Imaging Centre, The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London, UK.
  • Arvanitis TN; Neurosciences Research Section, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, UK.
  • Peet AC; The Children's Brain Tumour Research Centre, University of Nottingham, Nottingham, UK.
NMR Biomed ; 37(5): e5101, 2024 May.
Article em En | MEDLINE | ID: mdl-38303627
ABSTRACT
1H-magnetic resonance spectroscopy (MRS) has the potential to improve the noninvasive diagnostic accuracy for paediatric brain tumours. However, studies analysing large, comprehensive, multicentre datasets are lacking, hindering translation to widespread clinical practice. Single-voxel MRS (point-resolved single-voxel spectroscopy sequence, 1.5 T echo time [TE] 23-37 ms/135-144 ms, repetition time [TR] 1500 ms; 3 T TE 37-41 ms/135-144 ms, TR 2000 ms) was performed from 2003 to 2012 during routine magnetic resonance imaging for a suspected brain tumour on 340 children from five hospitals with 464 spectra being available for analysis and 281 meeting quality control. Mean spectra were generated for 13 tumour types. Mann-Whitney U-tests and Kruskal-Wallis tests were used to compare mean metabolite concentrations. Receiver operator characteristic curves were used to determine the potential for individual metabolites to discriminate between specific tumour types. Principal component analysis followed by linear discriminant analysis was used to construct a classifier to discriminate the three main central nervous system tumour types in paediatrics. Mean concentrations of metabolites were shown to differ significantly between tumour types. Large variability existed across each tumour type, but individual metabolites were able to aid discrimination between some tumour types of importance. Complete metabolite profiles were found to be strongly characteristic of tumour type and, when combined with the machine learning methods, demonstrated a diagnostic accuracy of 93% for distinguishing between the three main tumour groups (medulloblastoma, pilocytic astrocytoma and ependymoma). The accuracy of this approach was similar even when data of marginal quality were included, greatly reducing the proportion of MRS excluded for poor quality. Children's brain tumours are strongly characterised by MRS metabolite profiles readily acquired during routine clinical practice, and this information can be used to support noninvasive diagnosis. This study provides both key evidence and an important resource for the future use of MRS in the diagnosis of children's brain tumours.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Biomarcadores Tumorais Limite: Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Biomarcadores Tumorais Limite: Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article