HFE hemochromatosis in African Americans: Prevalence estimates of iron overload and iron overload-related disease

Am J Med Sci. 2023 Jan;365(1):31-36. doi: 10.1016/j.amjms.2022.08.015. Epub 2022 Sep 10.

Abstract

Background: Little is known about the prevalence of HFE (homeostatic iron regulator) hemochromatosis in African Americans (AA).

Methods: We defined AA as self-identified AA, blacks, or non-Hispanic blacks. We defined hemochromatosis-associated HFE genotypes as p.C282Y/p.C282Y and p.C282Y/p.H63D. We compiled prevalences of these genotypes in AA using published population and cohort data and numbers of men and women ≥18 y‬ in 2018 U.S. Census estimates. We defined iron overload (IO) and IO-related disease by genotype as previously reported in population and cohort studies of hemochromatosis in whites of European ancestry. We used these definitions to estimate prevalences and numbers of AA with IO and IO-related disease associated with hemochromatosis-associated HFE genotypes.

Results: There were ∼16,287,599 men and ∼17,644,898 women. HFE genotypes and their respective prevalences were: p.C282Y/p.C282Y, 0.00017 (6/34,905) [95% confidence interval 0.000034, 0.00031] and p.C282Y/p.H63D, 0.0012 (41/33,596) [0.000084, 0.0016]. IO prevalences were: men 0.000076 [0.000072, 0.000081] and women 0.0000061 [0.0000050, 0.0000073]. IO-related disease prevalences were: men 0.000063 [0.000059, 0.000067] and women 0.0000021 [0.0000014, 0.0000027]. There were ∼1021 [961, 1091] men and ∼36 [25, 48] women with IO-related disease.

Conclusions: We conclude that ∼1/25,061 AA >18 y have a hemochromatosis-associated HFE genotype and IO and that ∼1/32,103 AA >18 y have a hemochromatosis-associated HFE genotype and IO-related disease.

Keywords: p. H63D; p.C282Y; rs1799945; rs1800562.

MeSH terms

  • Adult
  • Black or African American / genetics
  • Female
  • Genotype
  • Hemochromatosis Protein / genetics
  • Hemochromatosis* / epidemiology
  • Hemochromatosis* / genetics
  • Histocompatibility Antigens Class I / genetics
  • Humans
  • Iron Overload* / epidemiology
  • Iron Overload* / genetics
  • Male
  • Mutation
  • Prevalence

Substances

  • Hemochromatosis Protein
  • HFE protein, human
  • Histocompatibility Antigens Class I