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

Authors :
Deelen, Joris
Kettunen, Johannes
Fischer, Krista
van der Spek, Ashley
Trompet, Stella
Kastenmüller, Gabi
Boyd, Andy
Zierer, Jonas
van den Akker, Erik B.
Ala-Korpela, Mika
Amin, Najaf
Demirkan, Ayse
Ghanbari, Mohsen
van Heemst, Diana
Ikram, Arfan
van Klinken, Jan Bert
Mooijaart, Simon P.
Peters, Annette
Salomaa, Veikko
Sattar, Naveed
Spector, Tim D.
Tiemeier, Henning
Verhoeven, Aswin
Waldenberger, Melanie
Würtz, Peter
Davey Smith, George
Metspalu, Andres
Perola, Markus
Menni, Cristina
Geleijnse, Johanna M.
Drenos, Fotios
Beekman, Marian
Jukema, Wouter
van Duijn, Cornelia M.
Slagboom, Eline
Deelen, Joris
Kettunen, Johannes
Fischer, Krista
van der Spek, Ashley
Trompet, Stella
Kastenmüller, Gabi
Boyd, Andy
Zierer, Jonas
van den Akker, Erik B.
Ala-Korpela, Mika
Amin, Najaf
Demirkan, Ayse
Ghanbari, Mohsen
van Heemst, Diana
Ikram, Arfan
van Klinken, Jan Bert
Mooijaart, Simon P.
Peters, Annette
Salomaa, Veikko
Sattar, Naveed
Spector, Tim D.
Tiemeier, Henning
Verhoeven, Aswin
Waldenberger, Melanie
Würtz, Peter
Davey Smith, George
Metspalu, Andres
Perola, Markus
Menni, Cristina
Geleijnse, Johanna M.
Drenos, Fotios
Beekman, Marian
Jukema, Wouter
van Duijn, Cornelia M.
Slagboom, Eline
Source :
ISSN: 2041-1723
Publication Year :
2019

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.

Details

Database :
OAIster
Journal :
ISSN: 2041-1723
Notes :
application/pdf, Nature Communications 10 (2019), ISSN: 2041-1723, ISSN: 2041-1723, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1200318961
Document Type :
Electronic Resource