A prospective evaluation of plasma polyphenol levels and colon cancer risk

Neil Murphy*, David Achaintre, Raul Zamora-Ros, Mazda Jenab, Marie Christine Boutron-Ruault, Franck Carbonnel, Isabelle Savoye, Rudolf Kaaks, Tilman Kühn, Heiner Boeing, Krasimira Aleksandrova, Anne Tjønneland, Cecilie Kyrø, Kim Overvad, J. Ramón Quirós, Maria Jose Sánchez, Jone M. Altzibar, José María Huerta, Aurelio Barricarte, Kay Tee KhawKathryn E. Bradbury, Aurora Perez-Cornago, Antonia Trichopoulou, Anna Karakatsani, Eleni Peppa, Domenico Palli, Sara Grioni, Rosario Tumino, Carlotta Sacerdote, Salvatore Panico, H. B(as) Bueno-de-Mesquita, Petra H. Peeters, Martin Rutegård, Ingegerd Johansson, Heinz Freisling, Hwayoung Noh, Amanda J. Cross, Paolo Vineis, Kostas Tsilidis, Marc J. Gunter, Augustin Scalbert

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)

Abstract

Polyphenols have been shown to exert biological activity in experimental models of colon cancer; however, human data linking specific polyphenols to colon cancer is limited. We assessed the relationship between pre-diagnostic plasma polyphenols and colon cancer risk in a case–control study nested within the European Prospective Investigation into Cancer and Nutrition study. Using high pressure liquid chromatography coupled to tandem mass spectrometry, we measured concentrations of 35 polyphenols in plasma from 809 incident colon cancer cases and 809 matched controls. We used multivariable adjusted conditional logistic regression models that included established colon cancer risk factors. The false discovery rate (qvalues) was computed to control for multiple comparisons. All statistical tests were two-sided. After false discovery rate correction and in continuous log2-transformed multivariable models, equol (odds ratio [OR] per log2-value, 0.86, 95% confidence interval [95% CI] = 0.79–0.93; qvalue = 0.01) and homovanillic acid (OR per log2-value, 1.46, 95% CI = 1.16–1.84; qvalue = 0.02) were associated with colon cancer risk. Comparing extreme fifths, equol concentrations were inversely associated with colon cancer risk (OR = 0.61, 95% CI = 0.41–0.91, ptrend = 0.003), while homovanillic acid concentrations were positively associated with colon cancer development (OR = 1.72, 95% CI = 1.17–2.53, ptrend < 0.0001). No heterogeneity for these associations was observed by sex and across other colon cancer risk factors. The remaining polyphenols were not associated with colon cancer risk. Higher equol concentrations were associated with lower risk, and higher homovanillic acid concentrations were associated with greater risk of colon cancer. These findings support a potential role for specific polyphenols in colon tumorigenesis.

Original languageEnglish
Pages (from-to)1620-1631
Number of pages12
JournalInternational Journal of Cancer
Volume143
Issue number7
DOIs
Publication statusPublished - 1 Oct 2018

Keywords

  • biomarkers
  • colon cancer
  • EPIC
  • nested case–control study
  • polyphenols

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