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

被引:0
作者
Palle Pedersen
Nils Milman
机构
[1] University of Copenhagen,Department of Clinical Biochemistry, Næstved Hospital
来源
Annals of Hematology | 2009年 / 88卷
关键词
Expressivity; Genotypes; Hemochromatosis; Mutations; Penetrance; Scandinavia;
D O I
暂无
中图分类号
学科分类号
摘要
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 ≥50%, ferritin ≥300 μg/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.
引用
收藏
页码:957 / 965
页数:8
相关论文
共 182 条
[1]  
Milman N(2001)Clinically overt hereditary hemochromatosis in Denmark 1948–1985: epidemiology, factors of significance for long-term survival, and causes of death in 179 patients Ann Hematol 80 737-744
[2]  
Pedersen P(2003)Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the Vikings Clin Genet 64 36-47
[3]  
Steig T(1998)The significance of haemochromatosis gene mutations in the general population: implications for screening Gut 43 830-836
[4]  
Byg K-E(1999)A population-based study of the clinical expression of the hemochromatosis gene N Engl J Med 341 718-724
[5]  
Graudal N(1999)Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri Am J Med 107 30-37
[6]  
Fenger K(2008)Clinical manifestations of hemochromatosis in HFE C282Y Homozygotes identified by screening Can J Gastroenterol 22 923-930
[7]  
Milman N(2002)Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients Blood Cells Mol Dis 29 41-47
[8]  
Pedersen P(2001)HFE mutations, iron deficiency and overload in 10, 500 blood donors Br J Haematol 114 474-484
[9]  
Burt MJ(2002)Penetrance of 845G A (C282Y) HFE hereditary haemochromatosis mutation in the USA Lancet 359 211-218
[10]  
George PM(2008)Iron overload related disease in N Engl J Med 358 221-230