Dietary Iron and Heme Iron Consumption, Genetic Susceptibility, and Risk of Crohn's Disease and Ulcerative Colitis
- PMID: 28604414
- PMCID: PMC5549140
- DOI: 10.1097/MIB.0000000000001161
Dietary Iron and Heme Iron Consumption, Genetic Susceptibility, and Risk of Crohn's Disease and Ulcerative Colitis
Abstract
Background: Dietary iron and heme, likely through their effect on gut commensal bacteria and colonic barrier function, have been shown to modulate colonic inflammation in animal models of colitis. Nonetheless, the link between dietary total and heme iron and risk of Crohn's disease (CD) and ulcerative colitis (UC) has not been previously explored.
Methods: We conducted a prospective cohort study of 165,331 U.S. women enrolled in the Nurses' Health Study and Nurses' Health Study II. Dietary information was collected using a validated food frequency questionnaire at baseline (1984) and updated every 2 to 4 years. Self-reported CD and UC diagnoses were confirmed through medical records review. We used Cox proportional hazard models to calculate hazard ratios and 95% confidence intervals while adjusting for potential confounders. In a case-control study nested within these cohorts, we evaluated the interaction between single-nucleotide polymorphisms associated with genome-wide susceptibility to CD and UC and dietary total and heme iron intake on risk of CD and UC using logistic regression modeling.
Results: Through 2011, over 3,038,049 person-years of follow-up, we documented 261 incident cases of CD and 321 incident cases of UC. Dietary heme iron was nonsignificantly associated with increased risk of UC (Ptrend = 0.12). This association seemed to be modified by the UC susceptibility locus, rs1801274, a coding variant in the FcγRIIA gene (Pinteraction = 7.00E-05). In contrast, there was no association between dietary heme iron and risk of CD (Ptrend = 0.67). We also did not observe an association between total dietary intake of iron and risk of CD or UC (All Ptrend > 0.35).
Conclusion: In 2 large prospective cohort studies, dietary total and heme iron were not associated with risk of CD or UC. Our suggestive finding that the association between dietary heme iron intake and risk of UC may be modified by a coding variant in FcγRIIA gene warrants additional investigation.
Conflict of interest statement
Comment in
-
Pumping Iron: Exploring Novel Gene-environment Interactions in the Inflammatory Bowel Diseases.Inflamm Bowel Dis. 2017 Jul;23(7):1096-1097. doi: 10.1097/MIB.0000000000001164. Inflamm Bowel Dis. 2017. PMID: 28604416 No abstract available.
References
-
- Zimmermann MB, Chassard C, Rohner F, et al. The effects of iron fortification on the gut microbiota in African children: a randomized controlled trial in Cote d’Ivoire. Am J Clin Nutr. 2010;92:1406–15. - PubMed
-
- Werner T, Wagner SJ, Martinez I, et al. Depletion of luminal iron alters the gut microbiota and prevents Crohn’s disease-like ileitis. Gut. 2011;60:325–33. - PubMed
-
- Young GP, Rose IS, St John DJ. Haem in the gut. I. Fate of haemoproteins and the absorption of haem. J Gastroenterol Hepatol. 1989;4:537–45. - PubMed
-
- Hunter DJ. Gene-environment interactions in human diseases. Nat Rev Genet. 2005;6:287–98. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 CA050385/CA/NCI NIH HHS/United States
- P01 CA087969/CA/NCI NIH HHS/United States
- K23 DK097142/DK/NIDDK NIH HHS/United States
- U01 CA067262/CA/NCI NIH HHS/United States
- K24 DK098311/DK/NIDDK NIH HHS/United States
- UM1 CA186107/CA/NCI NIH HHS/United States
- K08 DK064256/DK/NIDDK NIH HHS/United States
- R01 CA049449/CA/NCI NIH HHS/United States
- U01 CA049449/CA/NCI NIH HHS/United States
- K23 DK099681/DK/NIDDK NIH HHS/United States
- R01 CA067262/CA/NCI NIH HHS/United States
- P30 DK043351/DK/NIDDK NIH HHS/United States
- K01 DK110267/DK/NIDDK NIH HHS/United States
- K24 DK091417/DK/NIDDK NIH HHS/United States
- UM1 CA176726/CA/NCI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical