4.7 Article

1H-NMR urinary metabolomic profiling for diagnosis of gastric cancer

Journal

BRITISH JOURNAL OF CANCER
Volume 114, Issue 1, Pages 59-62

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/bjc.2015.414

Keywords

biomarkers; metabolomics; screening; gastric cancer; nuclear magnetic resonance

Categories

Funding

  1. Edmonton Civic Employees Charitable Assistance Fund
  2. Alberta Innovates Technology Futures Graduate Student Scholarship
  3. Dr D Schiller Academic Enrichment Fund
  4. Queen Elizabeth II Graduate Scholarship
  5. Government of Canada
  6. Alberta Heritage Foundation for Medical Research (AHFMR) Population Health Investigator Award from Alberta Innovates Health Solutions (AIHS)

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Background: Metabolomics has shown promise in gastric cancer (GC) detection. This research sought to identify whether GC has a unique urinary metabolomic profile compared with benign gastric disease (BN) and healthy (HE) patients. Methods: Urine from 43 GC, 40 BN, and 40 matched HE patients was analysed using H-1 nuclear magnetic resonance (H-1-NMR) spectroscopy, generating 77 reproducible metabolites (QC-RSD <25%). Univariate and multivariate (MVA) statistics were employed. A parsimonious biomarker profile of GC vs HE was investigated using LASSO regularised logistic regression (LASSO-LR). Model performance was assessed using Receiver Operating Characteristic (ROC) curves. Results: GC displayed a clear discriminatory biomarker profile; the BN profile overlapped with GC and HE. LASSO-LR identified three discriminatory metabolites: 2-hydroxyisobutyrate, 3-indoxylsulfate, and alanine, which produced a discriminatory model with an area under the ROC of 0.95. Conclusions: GC patients have a distinct urinary metabolite profile. This study shows clinical potential for metabolic profiling for early GC diagnosis.

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