Literature DB >> 19271219

Extrinsic factors modifying expressivity of the HFE variant C282Y, H63D, S65C phenotypes in 1,294 Danish men.

Palle Pedersen1, Nils Milman.   

Abstract

This study analysed the influence of extrinsic factors on the phenotypic expression of HFE gene variants in ethnic Danish men. A cohort of 6,020 men aged 30-53 years was screened for HFE C282Y, H63D and S65C variants. Serum iron, serum transferrin, transferrin saturation, and serum ferritin were analysed in 1,452 men and 1,294 men completed a questionnaire on factors, which could influence iron balance. The C282Y allele was present in 5.6%, H63D in 12.8% and S65C in 1.8% of the men. In the entire series, 3% had elevated iron status markers (transferrin saturation > or =50%, ferritin > or =300 microg/L). Self-reported liver disease had an elevating effect and peptic ulcer a lowering effect on iron status markers. Age increased the fraction of men with elevated ferritin from 8.3% at 32-38 years to 16.2% at 46-53 years of age (p = 0.002). Blood donation had a lowering effect on iron status markers (p = 0.0001). Alcohol consumption elevated serum iron and serum ferritin (p = 0.001). Meat consumption had an elevating effect (p = 0.02) and milk consumption a lowering effect (p = 0.03) on serum ferritin. There was no influence of vitamin-mineral tablets on iron status markers. In adjusted logistic regression analysis, the HFE genotype had the highest impact on iron status markers; high alcohol consumption was significantly associated with elevated transferrin saturation. High age and high alcohol consumption were significantly associated with elevated ferritin and high egg consumption and blood donation was significantly associated with normal ferritin levels. In conclusion, the expressivity of HFE variant phenotypes in Danish men was enhanced by alcohol and meat consumption and decreased by milk and egg consumption and blood donation.

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Year:  2009        PMID: 19271219     DOI: 10.1007/s00277-009-0714-x

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  9 in total

1.  Analysis of Familial Tendencies in Transferrin Saturation in a Korean Population.

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2.  Effects of strain and age on hepatic gene expression profiles in murine models of HFE-associated hereditary hemochromatosis.

Authors:  Seung-Min Lee; Alexandre Loguinov; Robert E Fleming; Christopher D Vulpe
Journal:  Genes Nutr       Date:  2014-11-27       Impact factor: 5.523

3.  A Review of Nutrients and Compounds, Which Promote or Inhibit Intestinal Iron Absorption: Making a Platform for Dietary Measures That Can Reduce Iron Uptake in Patients with Genetic Haemochromatosis.

Authors:  Nils Thorm Milman
Journal:  J Nutr Metab       Date:  2020-09-14

4.  Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Authors:  Gordon D McLaren; Victor R Gordeuk
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2009

5.  Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.

Authors:  Núria Aranda; Fernando E Viteri; Carme Montserrat; Victoria Arija
Journal:  Ann Hematol       Date:  2010-01-28       Impact factor: 3.673

Review 6.  Managing Genetic Hemochromatosis: An Overview of Dietary Measures, Which May Reduce Intestinal Iron Absorption in Persons With Iron Overload.

Authors:  Nils Thorm Milman
Journal:  Gastroenterology Res       Date:  2021-04-21

Review 7.  From Environment to Genome and Back: A Lesson from HFE Mutations.

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Journal:  Int J Mol Sci       Date:  2020-05-15       Impact factor: 5.923

Review 8.  Diagnosis and Treatment of Genetic HFE-Hemochromatosis: The Danish Aspect.

Authors:  Nils Thorm Milman; Frank Vinholt Schioedt; Anders Ellekaer Junker; Karin Magnussen
Journal:  Gastroenterology Res       Date:  2019-10-04

9.  EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH).

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  9 in total

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