Metabolite selection for machine learning in childhood brain tumour classification.

Autor: Zhao D; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK., Grist JT; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK., Rose HEL; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK., Davies NP; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK.; Imaging and Medical Physics, University Hospitals Birmingham, Birmingham, UK., Wilson M; Centre for Human Brain Health, University of Birmingham, Birmingham, UK., MacPherson L; Radiology, Birmingham Children's Hospital, Birmingham, UK., Abernethy LJ; Radiology, Alder Hey Children's Hospital, Liverpool, UK., Avula S; Radiology, Alder Hey Children's Hospital, Liverpool, UK., Pizer B; Paediatric Oncology, Alder Hey Children's Hospital, Liverpool, UK., Gutierrez DR; Children's Brain Tumour Research Centre, University of Nottingham, Nottingham, UK.; Medical Physics, Nottingham University Hospitals NHS Trust, Nottingham, UK., Jaspan T; Children's Brain Tumour Research Centre, University of Nottingham, Nottingham, UK.; Neuroradiology, Nottingham University Hospitals NHS Trust, Nottingham, UK., Morgan PS; Children's Brain Tumour Research Centre, University of Nottingham, Nottingham, UK.; Medical Physics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Division of Clinical Neuroscience, University of Nottingham, Nottingham, UK., Mitra D; Neuroradiology, The Newcastle upon Tyne Hospitals, Newcastle upon Tyne, UK., Bailey S; Paediatric Oncology, Great North Children's Hospital, Newcastle upon Tyne, UK., Sawlani V; Radiology, Queen Elizabeth Hospital Birmingham, Birmingham, UK.; School of Psychology, University of Birmingham, Birmingham, UK., Arvanitis TN; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK.; Institute of Digital Healthcare, WMG, University of Warwick, Coventry, UK., Sun Y; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK.; University of Birmingham and Southeast University Joint Research Centre for Biomedical Engineering, Suzhou, China., Peet AC; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.; Oncology, Birmingham Children's Hospital, Birmingham, UK.
Jazyk: angličtina
Zdroj: NMR in biomedicine [NMR Biomed] 2022 Jun; Vol. 35 (6), pp. e4673. Date of Electronic Publication: 2022 Jan 27.
DOI: 10.1002/nbm.4673
Abstrakt: MRS can provide high accuracy in the diagnosis of childhood brain tumours when combined with machine learning. A feature selection method such as principal component analysis is commonly used to reduce the dimensionality of metabolite profiles prior to classification. However, an alternative approach of identifying the optimal set of metabolites has not been fully evaluated, possibly due to the challenges of defining this for a multi-class problem. This study aims to investigate metabolite selection from in vivo MRS for childhood brain tumour classification. Multi-site 1.5 T and 3 T cohorts of patients with a brain tumour and histological diagnosis of ependymoma, medulloblastoma and pilocytic astrocytoma were retrospectively evaluated. Dimensionality reduction was undertaken by selecting metabolite concentrations through multi-class receiver operating characteristics and compared with principal component analysis. Classification accuracy was determined through leave-one-out and k-fold cross-validation. Metabolites identified as crucial in tumour classification include myo-inositol (P < 0.05, AUC = 0 . 81 ± 0 . 01 ), total lipids and macromolecules at 0.9 ppm (P < 0.05, AUC = 0 . 78 ± 0 . 01 ) and total creatine (P < 0.05, AUC = 0 . 77 ± 0 . 01 ) for the 1.5 T cohort, and glycine (P < 0.05, AUC = 0 . 79 ± 0 . 01 ), total N-acetylaspartate (P < 0.05, AUC = 0 . 79 ± 0 . 01 ) and total choline (P < 0.05, AUC = 0 . 75 ± 0 . 01 ) for the 3 T cohort. Compared with the principal components, the selected metabolites were able to provide significantly improved discrimination between the tumours through most classifiers (P < 0.05). The highest balanced classification accuracy determined through leave-one-out cross-validation was 85% for 1.5 T 1 H-MRS through support vector machine and 75% for 3 T 1 H-MRS through linear discriminant analysis after oversampling the minority. The study suggests that a group of crucial metabolites helps to achieve better discrimination between childhood brain tumours.
(© 2022 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd.)
Databáze: MEDLINE
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