TY - JOUR
T1 - A prospective evaluation of plasma polyphenol levels and colon cancer risk
AU - Murphy, Neil
AU - Achaintre, David
AU - Zamora-Ros, Raul
AU - Jenab, Mazda
AU - Boutron-Ruault, Marie Christine
AU - Carbonnel, Franck
AU - Savoye, Isabelle
AU - Kaaks, Rudolf
AU - Kühn, Tilman
AU - Boeing, Heiner
AU - Aleksandrova, Krasimira
AU - Tjønneland, Anne
AU - Kyrø, Cecilie
AU - Overvad, Kim
AU - Quirós, J. Ramón
AU - Sánchez, Maria Jose
AU - Altzibar, Jone M.
AU - María Huerta, José
AU - Barricarte, Aurelio
AU - Khaw, Kay Tee
AU - Bradbury, Kathryn E.
AU - Perez-Cornago, Aurora
AU - Trichopoulou, Antonia
AU - Karakatsani, Anna
AU - Peppa, Eleni
AU - Palli, Domenico
AU - Grioni, Sara
AU - Tumino, Rosario
AU - Sacerdote, Carlotta
AU - Panico, Salvatore
AU - Bueno-de-Mesquita, H. B(as)
AU - Peeters, Petra H.
AU - Rutegård, Martin
AU - Johansson, Ingegerd
AU - Freisling, Heinz
AU - Noh, Hwayoung
AU - Cross, Amanda J.
AU - Vineis, Paolo
AU - Tsilidis, Kostas
AU - Gunter, Marc J.
AU - Scalbert, Augustin
N1 - Publisher Copyright:
© 2018 The Authors International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - 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.
AB - 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.
KW - biomarkers
KW - colon cancer
KW - EPIC
KW - nested case–control study
KW - polyphenols
UR - http://www.scopus.com/inward/record.url?scp=85048790859&partnerID=8YFLogxK
U2 - 10.1002/ijc.31563
DO - 10.1002/ijc.31563
M3 - Article
AN - SCOPUS:85048790859
SN - 0020-7136
VL - 143
SP - 1620
EP - 1631
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 7
ER -