Higher vitamin B6 status is associated with improved survival among patients with stage I–III colorectal cancer

Andreana N. Holowatyj, Jennifer Ose, Biljana Gigic, Tengda Lin, Arve Ulvik, Anne J.M.R. Geijsen, Stefanie Brezina, Rama Kiblawi, Eline H. van Roekel, Andreas Baierl, Jürgen Böhm, Martijn J.L. Bours, Hermann Brenner, Stéphanie O. Breukink, Jenny Chang-Claude, Johannes H.W. de Wilt, William M. Grady, Thomas Grünberger, Tanja Gumpenberger, Esther HerpelMichael Hoffmeister, Eric T.P. Keulen, Dieuwertje E. Kok, Janna L. Koole, Katharina Kosma, Ewout A. Kouwenhoven, Gry Kvalheim, Christopher I. Li, Peter Schirmacher, Petra Schrotz-King, Marie C. Singer, Fränzel J.B. van Duijnhoven, Henk K. van Halteren, Kathy Vickers, F. Jeroen Vogelaar, Christy A. Warby, Evertine Wesselink, Per M. Ueland, Alexis B. Ulrich, Martin Schneider, Nina Habermann, Ellen Kampman, Matty P. Weijenberg, Andrea Gsur, Cornelia M. Ulrich

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Background: Folate-mediated 1-carbon metabolism requires several nutrients, including vitamin B6. Circulating biomarker concentrations indicating high vitamin B6 status are associated with a reduced risk of colorectal cancer (CRC). However, little is known about the effect of B6 status in relation to clinical outcomes in CRC patients. Objectives: We investigated survival outcomes in relation to vitamin B6 status in prospectively followed CRC patients. Methods: A total of 2031 patients with stage I–III CRC participated in 6 prospective patient cohorts in the international FOCUS (folate-dependent 1-carbon metabolism in colorectal cancer recurrence and survival) Consortium. Preoperative blood samples were used to measure vitamin B6 status by the direct marker pyridoxal 5'-phosphate (PLP), as well as the functional marker HK-ratio (HKr)[3'hydroxykynurenine: (kynurenic acid + xanthurenic acid + 3'-hydroxy anthranilic acid + anthranilic acid)]. Using Cox proportional hazards regression, we examined associations of vitamin B6 status with overall survival (OS), disease-free survival (DFS), and risk of recurrence, adjusted for patient age, sex, circulating creatinine concentrations, tumor site, stage, and cohort. Results: After a median follow-up of 3.2 y for OS, higher preoperative vitamin B6 status as assessed by PLP and the functional marker HKr was associated with 16–32% higher all-cause and disease-free survival, although there was no significant association with disease recurrence (doubling in PLP concentration: HROS, 0.68; 95% CI: 0.59, 0.79; HRDFS, 0.84; 95% CI: 0.75, 0.94; HRRecurrence, 0.96; 95% CI: 0.84, 1.09; HKr: HROS, 2.04; 95% CI: 1.67, 2.49; HRDFS, 1.56; 95% CI: 1.31, 1.85; HRRecurrence, 1.21; 95% CI: 0.96,1. 52). The association of PLP with improved OS was consistent across colorectal tumor site (right-sided colon: HROS, 0.75; 95% CI: 0.59, 0.96; left-sided colon: HROS, 0.71; 95% CI: 0.55, 0.92; rectosigmoid junction and rectum: HROS, 0.61; 95% CI: 0.47, 0.78). Conclusion: Higher preoperative vitamin B6 status is associated with improved OS among stage I–III CRC patients. Am J Clin Nutr 2022;116:303–313.
Original languageEnglish
Pages (from-to)303-313
Number of pages11
JournalAmerican Journal of Clinical Nutrition
Volume116
Issue number2
Early online date8 Apr 2022
DOIs
Publication statusPublished - Aug 2022
Externally publishedYes

Funding

ANH was supported by the National Institutes of Health under Ruth L. Kirschstein National Research Service Award T32 HG008962 from the National Human Genome Research Institute and the K12 HD043483 from the Eunice Kennedy Shriver National Institute of Child Health and Human Development. This work was also supported by grants from the National Institutes of Health/National Cancer Institute (U01 CA206110, R01 CA189184, and R01 CA207371 to CMU), the German Consortium of Translational Cancer Research (DKTK) and the German Cancer Research Center, the Matthias Lackas Foundation, Stiftung LebensBlicke, and Claussen-Simon Stiftung (Germany), the Huntsman Cancer Foundation, and the Immunology, Inflammation, and Infectious Disease Initiative at the University of Utah. This work was also supported by the European Research Area (ERA)-NET, JTC 2012 call on Translational Cancer Research (TRANSCAN). The research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health under Award Number P30 CA042014 and P30CA015704-40. The COLON study was supported by Wereld Kanker Onderzoek Fonds (WKOF) & World Cancer Research Fund International (WCRF International); the World Cancer Research Fund International Regular Grant Programme (WKOF/WCRF, the Netherlands, project no. 2014/1179); Alpe d’Huzes/Dutch Cancer Society (KWF Kankerbestrijding, the Netherlands, project no. UM 2012-5653, UW 2013-5927, UW 2015-7946); the Dutch Cancer Society (KWF Kankerbestrijding, the Netherlands; UM 2010-4867, and UM 2012-5653); ERA-NET on Translational Cancer Research (TRANSCAN/Dutch Cancer Society, the Netherlands, project no. UW 2013-6397, UW 2014-6877); the Netherlands Organization for Health Research and Development (ZonMw, the Netherlands); the Austrian Science Fund (FWF, Austria; project no. I 2104-B26); the Federal Ministry of Education and Research (BMBF, Germany; project no. 01KT1503); The Research Council of Norway (RCN, Norway; project no. 246402/H10). In addition, DEK is supported by a Veni grant (grant no. 016.Veni.188.082) of the Netherlands Organisation for Scientific Research. WMG is funded by the Fred Hutchinson Cancer Research Center, the Seattle Translational Tumor Research Program, and the Cottrell Family. EHvR was financially supported by Wereld Kanker Onderzoek Fonds (WKOF), as part of the World Cancer Research Fund International grant programme (grant no. 2016/1620). JLK and MJLB were financially supported by Kankeronderzoekfonds Limburg as part of Health Foundation Limburg (grant no. 00005739).

FundersFunder number
German Consortium of Translational Cancer Research
ERA-NET on Translational Cancer Research
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
National Institutes of Health
University of Utah
Deutschen Konsortium für Translationale Krebsforschung
Wereld Kanker Onderzoek Fonds
ZonMw
Stiftung LebensBlicke
Matthias Lackas-Stiftung
Huntsman Cancer Foundation
Claussen-Simon-Stiftung
Seattle Translational Tumor Research Program
Deutsches Krebsforschungszentrum
European Research AreaP30 CA042014, P30CA015704-40
World Cancer Research Fund2014/1179
National Cancer InstituteP30CA015704, R01CA207371, R01CA189184, U01CA206110
KWF KankerbestrijdingUM 2012-5653, UM 2010-4867, UW 2013-5927, UW 2015-7946
Austrian Science FundI 2104, 2104-B26
TRANSCANUW 2014-6877, UW 2013-6397
World Cancer Research Fund International00005739, 2016/1620
National Human Genome Research InstituteT32HG008962
Bundesministerium für Bildung und Forschung01KT1503
Norges forskningsråd246402/H10
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentK12HD043483

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