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Rigshospitalet - a part of Copenhagen University Hospital
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No Interaction between Polymorphisms Related to Vitamin A Metabolism and Vitamin A Intake in Relation to Colorectal Cancer in a Prospective Danish Cohort

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  1. Nutraceutical Supplements in the Thyroid Setting: Health Benefits beyond Basic Nutrition

    Research output: Contribution to journalReviewResearchpeer-review

  2. Bovine Milk Oligosaccharides with Sialyllactose Improves Cognition in Preterm Pigs

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  • Vibeke Andersen
  • Ulrich Halekoh
  • Torsten Bohn
  • Anne Tjønneland
  • Ulla Vogel
  • Tine Iskov Kopp
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Although vitamin A is essential for gut immune cell trafficking (paramount for the intestinal immune system), epidemiological studies on the role of vitamin A in colorectal cancer (CRC) aetiology are conflicting. By using functional polymorphisms, gene-environment (GxE) interaction analyses may identify the biological effects (or "mechanism of action") of environmental factors on CRC aetiology. Potential interactions between dietary or supplemental vitamin A intake and genetic variation in the vitamin A metabolic pathway genes related to risk of CRC were studied. We used a nested case-cohort design within the Danish "Diet, Cancer and Health" cohort, with prospectively collected lifestyle information from 57,053 participants, and the Cox proportional hazard models and likelihood ratio test. No statistically significant associations between the selected polymorphisms and CRC, and no statistically significant interactions between vitamin A intake and the polymorphisms were found. In conclusion, no support of an involvement of vitamin A in CRC aetiology was found.

Original languageEnglish
JournalNutrients
Volume11
Issue number6
Pages (from-to)1428
Number of pages15
ISSN2072-6643
DOIs
Publication statusPublished - 25 Jun 2019

    Research areas

  • Aged, Biomarkers, Tumor/genetics, Biotransformation, Case-Control Studies, Colorectal Neoplasms/epidemiology, Denmark/epidemiology, Female, Gene-Environment Interaction, Genetic Predisposition to Disease, Humans, Male, Middle Aged, Phenotype, Polymorphism, Genetic, Prospective Studies, Risk Factors, Vitamin A/administration & dosage

ID: 59098669