Metabolomic profiles predict individual multidisease outcomes

Thore Buergel(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Jakob Steinfeldt(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Greg Ruyoga(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Maik Pietzner(University of Cambridge), Daniele Bizzarri(Leiden University Medical Center), Dina Vojinović(Leiden University Medical Center), Julius Upmeier zu Belzen(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Lukas Loock(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Paul Kittner(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Lara Christmann(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Noah Hollmann(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Henrik Strangalies(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Jana M. Braunger(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Benjamin Wild(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Scott T. Chiesa(University College London), Joachim Spranger(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Fabian Klostermann(Humboldt-Universität zu Berlin), Erik B. van den Akker(Leiden University Medical Center), Stella Trompet(Leiden University Medical Center), Simon P. Mooijaart(Leiden University Medical Center), Naveed Sattar(University of Glasgow), J. Wouter Jukema(Leiden University Medical Center), Birgit D. A. Lavrijssen(Erasmus MC), Maryam Kavousi(Erasmus MC), Mohsen Ghanbari(Erasmus MC), M. Arfan Ikram(Erasmus MC), P. Eline Slagboom(Leiden University Medical Center), Mika Kivimäki(University of Helsinki), Claudia Langenberg(University of Cambridge), John Deanfield(University College London), Roland Eils(Heidelberg University), Ulf Landmesser(Berlin Institute of Health at Charité - Universitätsmedizin Berlin)
Nature Medicine
September 22, 2022
Cited by 386Open Access
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Abstract

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.


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