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Geographic and Racial/Ethnic Differences in HFEMutation Frequencies and Iron Phenotypes in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Authors :
Acton, Ronald T.
Snively, Beverly M.
Barton, James C.
Adams, Paul C.
Eckfeldt, John H.
Harris, Emily L.
Dawkins, Fitzroy W.
McLaren, Christine E.
Gordeuk, Victor R.
McLaren, Gordon D.
Reboussin, David M.
Sholinsky, Phyliss
Speechley, Mark R.
Holup, Joan
Leiendecker-Foster, Cathy
Source :
Blood; November 2004, Vol. 104 Issue: 11 p3211-3211, 1p
Publication Year :
2004

Abstract

Designing an optimal screening approach for hemochromatosis and iron overload requires knowledge of racial/ethnic subpopulations and frequencies of HFEmutations and phenotypes in geographic areas. In the HEIRS Study, HFEC282Y and H63D genotypes and prevalences of participants who met biochemical criteria for further evaluation (transferrin saturation >50% and ferritin >300 ng/mL, men; >45% and >200 ng/mL, women) were compared in a primary care-based sample of ~100,000 adults ≥25 years from 5 Field Centers. There were different respective HFEC282Y and H63D genotype frequencies in Whites, Blacks, Asians, and Hispanics across geographic areas (all p<0.0001), but not in Native Americans or Pacific Islanders. In Whites, the C282Y/C282Y proportion was significantly higher in AL than in CA or OR/HI. AL also had a significantly higher proportion of C282Y/wt than CA or OR/HI. In Blacks, D.C. had a significantly higher proportion of C282Y and H63D genotypes than AL. ONT had a significantly higher H63D genotype proportion than AL. In Asians, CA had a significantly higher proportion of H63D genotypes than OR/HI or ONT. In Hispanics, there were significant differences between: AL and CA; AL and D.C.; CA and D.C.; CA and OR/HI; D.C. and OR/HI; and D.C. and ONT. We also observed:

Details

Language :
English
ISSN :
00064971 and 15280020
Volume :
104
Issue :
11
Database :
Supplemental Index
Journal :
Blood
Publication Type :
Periodical
Accession number :
ejs56892737
Full Text :
https://doi.org/10.1182/blood.V104.11.3211.3211