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A reference map of potential determinants for the human serum metabolome

Author

Listed:
  • Noam Bar

    (Weizmann Institute of Science
    Weizmann Institute of Science)

  • Tal Korem

    (Weizmann Institute of Science
    Weizmann Institute of Science
    Columbia University Irving Medical Center
    Columbia University Irving Medical Center)

  • Omer Weissbrod

    (Weizmann Institute of Science
    Weizmann Institute of Science
    Harvard T.H. Chan School of Public Health)

  • David Zeevi

    (Weizmann Institute of Science
    Weizmann Institute of Science
    The Rockefeller University)

  • Daphna Rothschild

    (Weizmann Institute of Science
    Weizmann Institute of Science)

  • Sigal Leviatan

    (Weizmann Institute of Science
    Weizmann Institute of Science)

  • Noa Kosower

    (Weizmann Institute of Science
    Weizmann Institute of Science)

  • Maya Lotan-Pompan

    (Weizmann Institute of Science
    Weizmann Institute of Science)

  • Adina Weinberger

    (Weizmann Institute of Science
    Weizmann Institute of Science)

  • Caroline I. Roy

    (King’s College London)

  • Cristina Menni

    (King’s College London)

  • Alessia Visconti

    (King’s College London)

  • Mario Falchi

    (King’s College London)

  • Tim D. Spector

    (King’s College London)

  • Jerzy Adamski

    (Genome Analysis Center, Helmholtz Zentrum München, German Research Center for Environmental Health
    Technische Universität München
    National University of Singapore)

  • Paul W. Franks

    (Lund University
    Harvard T.H. Chan School of Public Health)

  • Oluf Pedersen

    (University of Copenhagen)

  • Eran Segal

    (Weizmann Institute of Science
    Weizmann Institute of Science)

Abstract

The serum metabolome contains a plethora of biomarkers and causative agents of various diseases, some of which are endogenously produced and some that have been taken up from the environment1. The origins of specific compounds are known, including metabolites that are highly heritable2,3, or those that are influenced by the gut microbiome4, by lifestyle choices such as smoking5, or by diet6. However, the key determinants of most metabolites are still poorly understood. Here we measured the levels of 1,251 metabolites in serum samples from a unique and deeply phenotyped healthy human cohort of 491 individuals. We applied machine-learning algorithms to predict metabolite levels in held-out individuals on the basis of host genetics, gut microbiome, clinical parameters, diet, lifestyle and anthropometric measurements, and obtained statistically significant predictions for more than 76% of the profiled metabolites. Diet and microbiome had the strongest predictive power, and each explained hundreds of metabolites—in some cases, explaining more than 50% of the observed variance. We further validated microbiome-related predictions by showing a high replication rate in two geographically independent cohorts7,8 that were not available to us when we trained the algorithms. We used feature attribution analysis9 to reveal specific dietary and bacterial interactions. We further demonstrate that some of these interactions might be causal, as some metabolites that we predicted to be positively associated with bread were found to increase after a randomized clinical trial of bread intervention. Overall, our results reveal potential determinants of more than 800 metabolites, paving the way towards a mechanistic understanding of alterations in metabolites under different conditions and to designing interventions for manipulating the levels of circulating metabolites.

Suggested Citation

  • Noam Bar & Tal Korem & Omer Weissbrod & David Zeevi & Daphna Rothschild & Sigal Leviatan & Noa Kosower & Maya Lotan-Pompan & Adina Weinberger & Caroline I. Roy & Cristina Menni & Alessia Visconti & Ma, 2020. "A reference map of potential determinants for the human serum metabolome," Nature, Nature, vol. 588(7836), pages 135-140, December.
  • Handle: RePEc:nat:nature:v:588:y:2020:i:7836:d:10.1038_s41586-020-2896-2
    DOI: 10.1038/s41586-020-2896-2
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    Citations

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    Cited by:

    1. Koen F. Dekkers & Sergi Sayols-Baixeras & Gabriel Baldanzi & Christoph Nowak & Ulf Hammar & Diem Nguyen & Georgios Varotsis & Louise Brunkwall & Nynne Nielsen & Aron C. Eklund & Jacob Bak Holm & H. Bj, 2022. "An online atlas of human plasma metabolite signatures of gut microbiome composition," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Efrat Muller & Itamar Shiryan & Elhanan Borenstein, 2024. "Multi-omic integration of microbiome data for identifying disease-associated modules," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    3. Saar Shoer & Smadar Shilo & Anastasia Godneva & Orly Ben-Yacov & Michal Rein & Bat Chen Wolf & Maya Lotan-Pompan & Noam Bar & Ervin I. Weiss & Yael Houri-Haddad & Yitzhak Pilpel & Adina Weinberger & E, 2023. "Impact of dietary interventions on pre-diabetic oral and gut microbiome, metabolites and cytokines," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    4. Shaza B. Zaghlool & Anna Halama & Nisha Stephan & Valborg Gudmundsdottir & Vilmundur Gudnason & Lori L. Jennings & Manonanthini Thangam & Emma Ahlqvist & Rayaz A. Malik & Omar M. E. Albagha & Abdul Ba, 2022. "Metabolic and proteomic signatures of type 2 diabetes subtypes in an Arab population," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    5. Kui Deng & Jin-jian Xu & Luqi Shen & Hui Zhao & Wanglong Gou & Fengzhe Xu & Yuanqing Fu & Zengliang Jiang & Menglei Shuai & Bang-yan Li & Wei Hu & Ju-Sheng Zheng & Yu-ming Chen, 2023. "Comparison of fecal and blood metabolome reveals inconsistent associations of the gut microbiota with cardiometabolic diseases," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    6. Petros Andrikopoulos & Judith Aron-Wisnewsky & Rima Chakaroun & Antonis Myridakis & Sofia K. Forslund & Trine Nielsen & Solia Adriouch & Bridget Holmes & Julien Chilloux & Sara Vieira-Silva & Gwen Fal, 2023. "Evidence of a causal and modifiable relationship between kidney function and circulating trimethylamine N-oxide," Nature Communications, Nature, vol. 14(1), pages 1-18, December.

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