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Metabolomic profiles predict individual multidisease outcomes
Risk stratification is critical for the early identification of high-risk individuals and disease prevention. Here we explored the potential of nuclear magnetic resonance (NMR) spectroscopy-derived metabolomic profiles to inform on multidisease risk beyond conventional clinical predictors for the on...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671812/ https://www.ncbi.nlm.nih.gov/pubmed/36138150 http://dx.doi.org/10.1038/s41591-022-01980-3 |
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author | Buergel, Thore Steinfeldt, Jakob Ruyoga, Greg Pietzner, Maik Bizzarri, Daniele Vojinovic, Dina Upmeier zu Belzen, Julius Loock, Lukas Kittner, Paul Christmann, Lara Hollmann, Noah Strangalies, Henrik Braunger, Jana M. Wild, Benjamin Chiesa, Scott T. Spranger, Joachim Klostermann, Fabian van den Akker, Erik B. Trompet, Stella Mooijaart, Simon P. Sattar, Naveed Jukema, J. Wouter Lavrijssen, Birgit Kavousi, Maryam Ghanbari, Mohsen Ikram, Mohammad A. Slagboom, Eline Kivimaki, Mika Langenberg, Claudia Deanfield, John Eils, Roland Landmesser, Ulf |
author_facet | Buergel, Thore Steinfeldt, Jakob Ruyoga, Greg Pietzner, Maik Bizzarri, Daniele Vojinovic, Dina Upmeier zu Belzen, Julius Loock, Lukas Kittner, Paul Christmann, Lara Hollmann, Noah Strangalies, Henrik Braunger, Jana M. Wild, Benjamin Chiesa, Scott T. Spranger, Joachim Klostermann, Fabian van den Akker, Erik B. Trompet, Stella Mooijaart, Simon P. Sattar, Naveed Jukema, J. Wouter Lavrijssen, Birgit Kavousi, Maryam Ghanbari, Mohsen Ikram, Mohammad A. Slagboom, Eline Kivimaki, Mika Langenberg, Claudia Deanfield, John Eils, Roland Landmesser, Ulf |
author_sort | Buergel, Thore |
collection | PubMed |
description | Risk stratification is critical for the early identification of high-risk individuals and disease prevention. Here we explored the potential of nuclear magnetic resonance (NMR) spectroscopy-derived metabolomic profiles to inform on multidisease risk beyond conventional clinical predictors for the onset of 24 common conditions, including metabolic, vascular, respiratory, musculoskeletal and neurological diseases and cancers. Specifically, we trained a neural network to learn disease-specific metabolomic states from 168 circulating metabolic markers measured in 117,981 participants with ~1.4 million person-years of follow-up from the UK Biobank and validated the model in four independent cohorts. We found metabolomic states to be associated with incident event rates in all the investigated conditions, except breast cancer. For 10-year outcome prediction for 15 endpoints, with and without established metabolic contribution, a combination of age and sex and the metabolomic state equaled or outperformed established predictors. Moreover, metabolomic state added predictive information over comprehensive clinical variables for eight common diseases, including type 2 diabetes, dementia and heart failure. Decision curve analyses showed that predictive improvements translated into clinical utility for a wide range of potential decision thresholds. Taken together, our study demonstrates both the potential and limitations of NMR-derived metabolomic profiles as a multidisease assay to inform on the risk of many common diseases simultaneously. |
format | Online Article Text |
id | pubmed-9671812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-96718122022-11-19 Metabolomic profiles predict individual multidisease outcomes Buergel, Thore Steinfeldt, Jakob Ruyoga, Greg Pietzner, Maik Bizzarri, Daniele Vojinovic, Dina Upmeier zu Belzen, Julius Loock, Lukas Kittner, Paul Christmann, Lara Hollmann, Noah Strangalies, Henrik Braunger, Jana M. Wild, Benjamin Chiesa, Scott T. Spranger, Joachim Klostermann, Fabian van den Akker, Erik B. Trompet, Stella Mooijaart, Simon P. Sattar, Naveed Jukema, J. Wouter Lavrijssen, Birgit Kavousi, Maryam Ghanbari, Mohsen Ikram, Mohammad A. Slagboom, Eline Kivimaki, Mika Langenberg, Claudia Deanfield, John Eils, Roland Landmesser, Ulf Nat Med Article Risk stratification is critical for the early identification of high-risk individuals and disease prevention. Here we explored the potential of nuclear magnetic resonance (NMR) spectroscopy-derived metabolomic profiles to inform on multidisease risk beyond conventional clinical predictors for the onset of 24 common conditions, including metabolic, vascular, respiratory, musculoskeletal and neurological diseases and cancers. Specifically, we trained a neural network to learn disease-specific metabolomic states from 168 circulating metabolic markers measured in 117,981 participants with ~1.4 million person-years of follow-up from the UK Biobank and validated the model in four independent cohorts. We found metabolomic states to be associated with incident event rates in all the investigated conditions, except breast cancer. For 10-year outcome prediction for 15 endpoints, with and without established metabolic contribution, a combination of age and sex and the metabolomic state equaled or outperformed established predictors. Moreover, metabolomic state added predictive information over comprehensive clinical variables for eight common diseases, including type 2 diabetes, dementia and heart failure. Decision curve analyses showed that predictive improvements translated into clinical utility for a wide range of potential decision thresholds. Taken together, our study demonstrates both the potential and limitations of NMR-derived metabolomic profiles as a multidisease assay to inform on the risk of many common diseases simultaneously. Nature Publishing Group US 2022-09-22 2022 /pmc/articles/PMC9671812/ /pubmed/36138150 http://dx.doi.org/10.1038/s41591-022-01980-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Buergel, Thore Steinfeldt, Jakob Ruyoga, Greg Pietzner, Maik Bizzarri, Daniele Vojinovic, Dina Upmeier zu Belzen, Julius Loock, Lukas Kittner, Paul Christmann, Lara Hollmann, Noah Strangalies, Henrik Braunger, Jana M. Wild, Benjamin Chiesa, Scott T. Spranger, Joachim Klostermann, Fabian van den Akker, Erik B. Trompet, Stella Mooijaart, Simon P. Sattar, Naveed Jukema, J. Wouter Lavrijssen, Birgit Kavousi, Maryam Ghanbari, Mohsen Ikram, Mohammad A. Slagboom, Eline Kivimaki, Mika Langenberg, Claudia Deanfield, John Eils, Roland Landmesser, Ulf Metabolomic profiles predict individual multidisease outcomes |
title | Metabolomic profiles predict individual multidisease outcomes |
title_full | Metabolomic profiles predict individual multidisease outcomes |
title_fullStr | Metabolomic profiles predict individual multidisease outcomes |
title_full_unstemmed | Metabolomic profiles predict individual multidisease outcomes |
title_short | Metabolomic profiles predict individual multidisease outcomes |
title_sort | metabolomic profiles predict individual multidisease outcomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671812/ https://www.ncbi.nlm.nih.gov/pubmed/36138150 http://dx.doi.org/10.1038/s41591-022-01980-3 |
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