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Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders

Untargeted metabolomics (UM) allows for the simultaneous measurement of hundreds of metabolites in a single analytical run. The sheer amount of data generated in UM hampers its use in patient diagnostics because manual interpretation of all features is not feasible. Here, we describe the application...

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Autores principales: Hoegen, Brechtje, Hampstead, Juliet E., Engelke, Udo F.H., Kulkarni, Purva, Wevers, Ron A., Brunner, Han G., Coene, Karlien L. M., Gilissen, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544878/
https://www.ncbi.nlm.nih.gov/pubmed/35546254
http://dx.doi.org/10.1002/jimd.12522
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author Hoegen, Brechtje
Hampstead, Juliet E.
Engelke, Udo F.H.
Kulkarni, Purva
Wevers, Ron A.
Brunner, Han G.
Coene, Karlien L. M.
Gilissen, Christian
author_facet Hoegen, Brechtje
Hampstead, Juliet E.
Engelke, Udo F.H.
Kulkarni, Purva
Wevers, Ron A.
Brunner, Han G.
Coene, Karlien L. M.
Gilissen, Christian
author_sort Hoegen, Brechtje
collection PubMed
description Untargeted metabolomics (UM) allows for the simultaneous measurement of hundreds of metabolites in a single analytical run. The sheer amount of data generated in UM hampers its use in patient diagnostics because manual interpretation of all features is not feasible. Here, we describe the application of a pathway‐based metabolite set enrichment analysis method to prioritise relevant biological pathways in UM data. We validate our method on a set of 55 patients with a diagnosed inherited metabolic disorder (IMD) and show that it complements feature‐based prioritisation of biomarkers by placing the features in a biological context. In addition, we find that by taking enriched pathways shared across different IMDs, we can identify common drugs and compounds that could otherwise obscure genuine disease biomarkers in an enrichment method. Finally, we demonstrate the potential of this method to identify novel candidate biomarkers for known IMDs. Our results show the added value of pathway‐based interpretation of UM data in IMD diagnostics context.
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spelling pubmed-95448782022-10-14 Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders Hoegen, Brechtje Hampstead, Juliet E. Engelke, Udo F.H. Kulkarni, Purva Wevers, Ron A. Brunner, Han G. Coene, Karlien L. M. Gilissen, Christian J Inherit Metab Dis Original Articles Untargeted metabolomics (UM) allows for the simultaneous measurement of hundreds of metabolites in a single analytical run. The sheer amount of data generated in UM hampers its use in patient diagnostics because manual interpretation of all features is not feasible. Here, we describe the application of a pathway‐based metabolite set enrichment analysis method to prioritise relevant biological pathways in UM data. We validate our method on a set of 55 patients with a diagnosed inherited metabolic disorder (IMD) and show that it complements feature‐based prioritisation of biomarkers by placing the features in a biological context. In addition, we find that by taking enriched pathways shared across different IMDs, we can identify common drugs and compounds that could otherwise obscure genuine disease biomarkers in an enrichment method. Finally, we demonstrate the potential of this method to identify novel candidate biomarkers for known IMDs. Our results show the added value of pathway‐based interpretation of UM data in IMD diagnostics context. John Wiley & Sons, Inc. 2022-05-22 2022-07 /pmc/articles/PMC9544878/ /pubmed/35546254 http://dx.doi.org/10.1002/jimd.12522 Text en © 2022 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Hoegen, Brechtje
Hampstead, Juliet E.
Engelke, Udo F.H.
Kulkarni, Purva
Wevers, Ron A.
Brunner, Han G.
Coene, Karlien L. M.
Gilissen, Christian
Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
title Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
title_full Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
title_fullStr Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
title_full_unstemmed Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
title_short Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
title_sort application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544878/
https://www.ncbi.nlm.nih.gov/pubmed/35546254
http://dx.doi.org/10.1002/jimd.12522
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