Vitamins B2 and B6 and Genetic Polymorphisms Related to One-Carbon Metabolism as Risk Factors for Gastric Adenocarcinoma in the European Prospective Investigation into Cancer and Nutrition

Simone J. P. M. Eussen, Stein Emil Vollset, Steinar Hustad, Oivind Midttun, Klaus Meyer, Ase Fredriksen, Per Magne Ueland, Mazda Jenab, Nadia Slimani, Pietro Ferrari, Antonio Agudo, Nuria Sala, Gabriel Capella, Giuseppe Del Giudice, Domenico Palli, Heiner Boeing, Cornelia Weikert, H. Bas Bueno-de-Mesquita, Frederike L. Buechner, Fatima CarneiroFranco Berrino, Paolo Vineis, Rosario Tumino, Salvatore Panico, Göran Berglund, Jonas Manjer, Roger Stenling, Goeran Hallmans, Carmen Martinez, Larraitz Arrizola, Aurelio Barricarte, Carmen Navarro, Laudina Rodriguez, Sheila Bingham, Jakob Linseisen, Rudolf Kaaks, Kim Overvad, Anne Tjonneland, Petra H. M. Peeters, Mattijs E. Numans, Francoise Clavel-Chapelon, Marie-Christine Boutron-Ruault, Sophie Morois, Antonia Trichopoulou, Eiliv Lund, Mario Plebani, Elio Riboli, Carlos A. Gonzalez

Research output: Contribution to journalArticlepeer-review

Abstract

B vitamins and polymorphisms in genes coding for enzymes involved in one-carbon metabolism may affect DNA synthesis and methylation and thereby be implicated in carcinogenesis. Previous data on vitamins B2 and B6 and genetic polymorphisms other than those involving MTHFR as risk factors for gastric cancer (GC) are sparse and inconsistent. In this case-control study nested within the European Prospective Investigation into Cancer and Nutrition cohort, cases (n = 235) and controls (n = 601) were matched for study center, age, sex, and time of blood sampling. B2 and B6 species were measured in plasma, and the sum of riboflavin and flavin mononucleotide was used as the main exposure variable for vitamin 132 status, whereas the sum of pyridoxal 5'-phosphate, pyridoxal, and 4-pyridoxic acid was used to define vitamin B6 status. In addition, we determined eight polymorphisms related to one-carbon metabolism. Relative risks for CC risk were calculated with conditional logistic regression, adjusted for Helicobacter pylori infection status and smoking status. Adjusted relative risks per quartile (95% confidence interval, P-trend) were 0.85 (0.72-1.01, 0.06) for vitamin B2 and 0.78 (0.65-0.93, <0.01) for vitamin B6. Both relations were stronger in individuals with severe chronic atrophic gastritis. The polymorphisms were not associated with CC risk and did not modify the observed vitamin-cancer associations. In summary, results from this large European cohort study showed an inverse association between vitamin B2 and CC risk, which is borderline significant, and a significant inverse association between vitamin B6 and CC risk. Cancer Epidemiol Biomarkers Prev; 19(1); 28-38. (C)2010 AACR.
Original languageEnglish
Pages (from-to)28-38
JournalCancer Epidemiology Biomarkers & Prevention
Volume19
Issue number1
DOIs
Publication statusPublished - 2010

Subject classification (UKÄ)

  • Cancer and Oncology

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