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Targeted Plasma Metabolic Profiles and Risk of Recurrence in Stage II and III Colorectal Cancer Patients: Results from an International Cohort Consortium.

Authors :
Ose, Jennifer
Gigic, Biljana
Brezina, Stefanie
Lin, Tengda
Baierl, Andreas
Geijsen, Anne J. M. R.
van Roekel, Eline
Robinot, Nivonirina
Gicquiau, Audrey
Achaintre, David
Keski-Rahkonen, Pekka
van Duijnhoven, Fränzel J. B.
Gumpenberger, Tanja
Holowatyj, Andreana N.
Kok, Dieuwertje E.
Koole, Annaleen
Schrotz-King, Petra
Ulrich, Alexis B.
Schneider, Martin
Ulvik, Arve
Source :
Metabolites (2218-1989); Mar2021, Vol. 11 Issue 3, p129, 1p
Publication Year :
2021

Abstract

The identification of patients at high-risk for colorectal cancer (CRC) recurrence remains an unmet clinical need. The aim of this study was to investigate associations of metabolites with risk of recurrence in stage II/III CRC patients. A targeted metabolomics assay (128 metabolites measured) was performed on pre-surgery collected EDTA plasma samples from n = 440 newly diagnosed stage II/III CRC patients. Patients have been recruited from four prospective cohort studies as part of an international consortium: Metabolomic profiles throughout the continuum of CRC (MetaboCCC). Cox proportional hazard models were computed to investigate associations of metabolites with recurrence, adjusted for age, sex, tumor stage, tumor site, body mass index, and cohort; false discovery rate (FDR) was used to account for multiple testing. Sixty-nine patients (15%) had a recurrence after a median follow-up time of 20 months. We identified 13 metabolites that were nominally associated with a reduced risk of recurrence. None of the associations were statistically significant after controlling for multiple testing. Pathway topology analyses did not reveal statistically significant associations between recurrence and alterations in metabolic pathways (e.g., sphingolipid metabolism p = 0.04; pFDR = 1.00). To conclude, we did not observe statistically significant associations between metabolites and CRC recurrence using a well-established metabolomics assay. The observed results require follow-up in larger studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22181989
Volume :
11
Issue :
3
Database :
Complementary Index
Journal :
Metabolites (2218-1989)
Publication Type :
Academic Journal
Accession number :
149514333
Full Text :
https://doi.org/10.3390/metabo11030129