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Human postprandial responses to food and potential for precision nutrition

Berry, Sarah E.; Valdes, Ana M.; Drew, David A.; Asnicar, Francesco; Mazidi, Mohsen; Wolf, Jonathan; Capdevila, Joan; Hadjigeorgiou, George; Davies, Richard; Al Khatib, Haya; Bonnett, Christopher; Ganesh, Sajaysurya; Bakker, Elco; Hart, Deborah; Mangino, Massimo; Merino, Jordi; Linenberg, Inbar; Wyatt, Patrick; Ordovas, Jose M.; Gardner, Christopher D.; Delahanty, Linda M.; Chan, Andrew T.; Segata, Nicola; Franks, Paul W.; Spector, Tim D.

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Authors

Sarah E. Berry

David A. Drew

Francesco Asnicar

Mohsen Mazidi

Jonathan Wolf

Joan Capdevila

George Hadjigeorgiou

Richard Davies

Haya Al Khatib

Christopher Bonnett

Sajaysurya Ganesh

Elco Bakker

Deborah Hart

Massimo Mangino

Jordi Merino

Inbar Linenberg

Patrick Wyatt

Jose M. Ordovas

Christopher D. Gardner

Linda M. Delahanty

Andrew T. Chan

Nicola Segata

Paul W. Franks

Tim D. Spector



Abstract

Metabolic responses to food influence risk of cardiometabolic disease, but large-scale high-resolution studies are lacking. We recruited n = 1,002 twins and unrelated healthy adults in the United Kingdom to the PREDICT 1 study and assessed postprandial metabolic responses in a clinical setting and at home. We observed large inter-individual variability (as measured by the population coefficient of variation (s.d./mean, %)) in postprandial responses of blood triglyceride (103%), glucose (68%) and insulin (59%) following identical meals. Person-specific factors, such as gut microbiome, had a greater influence (7.1% of variance) than did meal macronutrients (3.6%) for postprandial lipemia, but not for postprandial glycemia (6.0% and 15.4%, respectively); genetic variants had a modest impact on predictions (9.5% for glucose, 0.8% for triglyceride, 0.2% for C-peptide). Findings were independently validated in a US cohort (n = 100 people). We developed a machine-learning model that predicted both triglyceride (r = 0.47) and glycemic (r = 0.77) responses to food intake. These findings may be informative for developing personalized diet strategies. The ClinicalTrials.gov registration identifier is NCT03479866.

Citation

Berry, S. E., Valdes, A. M., Drew, D. A., Asnicar, F., Mazidi, M., Wolf, J., Capdevila, J., Hadjigeorgiou, G., Davies, R., Al Khatib, H., Bonnett, C., Ganesh, S., Bakker, E., Hart, D., Mangino, M., Merino, J., Linenberg, I., Wyatt, P., Ordovas, J. M., Gardner, C. D., …Spector, T. D. (2020). Human postprandial responses to food and potential for precision nutrition. Nature Medicine, 26, 964-973. https://doi.org/10.1038/s41591-020-0934-0

Journal Article Type Article
Acceptance Date May 22, 2020
Online Publication Date Jun 11, 2020
Publication Date Jun 11, 2020
Deposit Date Jun 14, 2020
Publicly Available Date Dec 12, 2020
Journal Nature Medicine
Print ISSN 1078-8956
Electronic ISSN 1546-170X
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 26
Pages 964-973
DOI https://doi.org/10.1038/s41591-020-0934-0
Keywords General Biochemistry, Genetics and Molecular Biology; General Medicine
Public URL https://nottingham-repository.worktribe.com/output/4646169
Publisher URL https://www.nature.com/articles/s41591-020-0934-0
Additional Information A Publisher Correction to this article was published on 20 October 2020: https://www.nature.com/articles/s41591-020-1130-y

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