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Deelen, J.* ; Kettunen, J.* ; Fischer, K.* ; van der Spek, A.* ; Trompet, S.* ; Kastenmüller, G. ; Boyd, A.W.* ; Zierer, J. ; van den Akker, E.B.* ; Amin, N.* ; Demirkan, A.* ; Ghanbari, M.* ; van Heemst, D.* ; Ikram, M.A.* ; van Klinken, J.B.* ; Mooijaart, S.P.* ; Peters, A. ; Salomaa, V.* ; Sattar, N.* ; Spector, T.D.* ; Tiemeier, H.* ; Verhoeven, A.* ; Waldenberger, M. ; Würtz, P.* ; Davey Smith, G.* ; Metspalu, A.* ; Perola, M.* ; Menni, C.* ; Geleijnse, J.M.* ; Drenos, F.* ; Beekman, M.* ; Jukema, J.W.* ; van Duijn, C.M.* ; Slagboom, P.E.*

A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals.

Nat. Commun. 10:3346 (2019)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Predicting longer-term mortality risk requires collection of clinical data, which is often cumbersome. Therefore, we use a well-standardized metabolomics platform to identify metabolic predictors of long-term mortality in the circulation of 44,168 individuals (age at baseline 18-109), of whom 5512 died during follow-up. We apply a stepwise (forward-backward) procedure based on meta-analysis results and identify 14 circulating biomarkers independently associating with all-cause mortality. Overall, these associations are similar in men and women and across different age strata. We subsequently show that the prediction accuracy of 5- and 10-year mortality based on a model containing the identified biomarkers and sex (C-statistic = 0.837 and 0.830, respectively) is better than that of a model containing conventional risk factors for mortality (C-statistic = 0.772 and 0.790, respectively). The use of the identified metabolic profile as a predictor of mortality or surrogate endpoint in clinical studies needs further investigation.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Magnetic-resonance Metabolomics; Amino-acids; Association; Hyperglycemia; Epidemiology
Sprache englisch
Veröffentlichungsjahr 2019
HGF-Berichtsjahr 2019
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 10, Heft: 1, Seiten: , Artikelnummer: 3346 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Bioinformatics and Systems Biology (IBIS)
Institute of Epidemiology (EPI)
POF Topic(s) 30505 - New Technologies for Biomedical Discoveries
30202 - Environmental Health
Forschungsfeld(er) Enabling and Novel Technologies
Genetics and Epidemiology
PSP-Element(e) G-503700-001
G-504000-010
G-504091-001
DOI 10.1038/s41467-019-11311-9
WOS ID WOS:000481748600001
Scopus ID 85070837796
PubMed ID 31431621
Erfassungsdatum 2019-09-19
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