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

Joris Deelen(Leiden University Medical Center), Johannes Kettunen(Finnish Institute for Health and Welfare), Krista Fischer(University of Tartu), Ashley van der Spek(Erasmus MC), Stella Trompet(Leiden University Medical Center), Gabi Kastenmüller(St Thomas' Hospital), Andy Boyd(University of Bristol), Jonas Zierer(Novartis (Switzerland)), Erik B. van den Akker(Leiden University Medical Center), Mika Ala‐Korpela(Baker Heart and Diabetes Institute), Najaf Amin(Erasmus MC), Ayşe Demirkan(University Medical Center Groningen), Mohsen Ghanbari(Mashhad University of Medical Sciences), Diana van Heemst(Leiden University Medical Center), M. Arfan Ikram(Erasmus MC), Jan B. van Klinken(Leiden University Medical Center), Simon P. Mooijaart(Leiden University Medical Center), Annette Peters(Helmholtz Zentrum München), Veikko Salomaa(Finnish Institute for Health and Welfare), Naveed Sattar(University of Glasgow), Tim D. Spector(St Thomas' Hospital), Henning Tiemeier(Erasmus MC), Aswin Verhoeven(Leiden University Medical Center), Mélanie Waldenberger(Helmholtz Zentrum München), Peter Würtz, George Davey Smith(University of Bristol), Andres Metspalu(University of Tartu), Markus Perola(University of Helsinki), Cristina Menni(St Thomas' Hospital), Johanna M. Geleijnse(Wageningen University & Research), Fotios Drenos(University of Bristol), Marian Beekman(Leiden University Medical Center), J. Wouter Jukema(Leiden University Medical Center), Cornelia M. van Duijn(Leiden University), P. Eline Slagboom(Leiden University Medical Center)
Nature Communications
August 20, 2019
Cited by 374Open Access
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Abstract

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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