SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent

被引:24
作者
Barton, James C.
Acton, Ronald T.
Lee, Pauline L.
West, Carol
机构
[1] So Iron Disorders Ctr, Birmingham, AL 35209 USA
[2] Univ Alabama, Dept Microbiol Med & Epidemiol, Birmingham, AL 35294 USA
[3] Univ Alabama, Dept Int Hlth, Birmingham, AL 35294 USA
[4] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
关键词
ferroportin; genetics; hemojuvelin A310G; mutation;
D O I
10.1016/j.bcmd.2007.03.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The ferroportin polymorphism SLC40A1 Q248H (exon 6, cDNA 744G -> T; Gln248His) occurs in persons of sub-Saharan African descent with and without iron overload, and is associated with elevated serum ferritin concentrations (SF). However, the risk of iron overload associated with Q248H has not been defined. We tabulated previously reported Q248H allele frequency estimates in African -Americans and Native Africans, and computed the risk of iron overload associated with Q248H in subjects who lacked HFE C282Y. The aggregate Q248H allele frequency in 1038 African-Americans in two cohorts from Alabama and one cohort each from Washington, DC and California was 0.0525 (95% CI: 0.0451, 0.0652); there was no significant difference in frequencies across these cohorts. The aggregate frequency in 259 Natives from southeast Africa in two cohorts was 0.0946 (95% CI: 0.0694, 0.1198); the difference between the frequencies of these cohorts was riot significant. The aggregate Q248H frequencies in African-Americans and Native Africans differed significantly (0.0525 vs. 0.0946, respectively; p = 0.002 1). There were reports of 24 unrelated African-Americans and 15 unrelated Native Africans without HFE C282Y who had iron overload. In African-Americans, the odds ratio (OR) of Q248H-associated risk of iron overload using 610 C282Y-negative control subjects unselected for SF was 1.57 (95% CI: 0.52, 4.72; p=0.29). In Native Africans, the OR using 208 control subjects unselected for SF was 1.05 (95% Cl: 0.28, 3.90;p=0.58). We conclude that the frequency of SLC40A1 Q248H is significantly lower in African-Americans than in Native Africans. Although OR estimates of iron overload in African -Americans and Native Africans with Q248H were greater than unity, the increased OR were not statistically significant. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:206 / 211
页数:6
相关论文
共 45 条
[31]   Ferroportin (Q248H) mutations in African families with dietary iron overload [J].
Mcnamara, L ;
Gordeuk, VR ;
MacPhail, AP .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2005, 20 (12) :1855-1858
[32]  
McNamara L, 1998, BRIT J HAEMATOL, V102, P1176
[33]   Geography of HFE C282Y and H63D mutations [J].
Merryweather-Clarke, AT ;
Pointon, JJ ;
Jouanolle, AM ;
Rochette, J ;
Robson, KJH .
GENETIC TESTING, 2000, 4 (02) :183-198
[34]   Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene [J].
Montosi, G ;
Donovan, A ;
Totaro, A ;
Garuti, C ;
Pignatti, E ;
Cassanelli, S ;
Trenor, CC ;
Gasparini, P ;
Andrews, NC ;
Pietrangelo, A .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (04) :619-623
[35]  
*NAT I HLTH, 2007, UN ORG VIEW TRANSCR
[36]   Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization [J].
Nemeth, E ;
Tuttle, MS ;
Powelson, J ;
Vaughn, MB ;
Donovan, A ;
Ward, DM ;
Ganz, T ;
Kaplan, J .
SCIENCE, 2004, 306 (5704) :2090-2093
[37]   Non-HFE hemochromatosis [J].
Pietrangelo, A .
SEMINARS IN LIVER DISEASE, 2005, 25 (04) :450-460
[38]   Association of ferroportin Q248H polymorphism with elevated levels of serum ferritin in African Americans in the Hemochromatosis and Iron Overload Screening (HEIRS) Study [J].
River, Charles A. ;
Barton, James C. ;
Gordeuk, Victor R. ;
Acton, Ronald T. ;
Speechley, Mark R. ;
Snively, Beverly M. ;
Leiendecker-Foster, Catherine ;
Press, Richard D. ;
Adams, Paul C. ;
McLaren, Gordon D. ;
Dawkins, Fitzroy W. ;
McLaren, Christine E. ;
Reboussin, David M. .
BLOOD CELLS MOLECULES AND DISEASES, 2007, 38 (03) :247-252
[39]   To the editor: A valine deletion of ferroportin 1: a common mutation in hemochromatosis type 4? [J].
Roetto, A ;
Merryweather-Clarke, AT ;
Daraio, F ;
Livesey, K ;
Pointon, JJ ;
Barbabietola, G ;
Piga, A ;
Mackie, PH ;
Robson, KJH ;
Camaschella, C .
BLOOD, 2002, 100 (02) :733-734
[40]   In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations [J].
Schimanski, LM ;
Drakesmith, H ;
Merryweather-Clarke, AT ;
Viprakasit, V ;
Edwards, JP ;
Sweetland, E ;
Bastin, JM ;
Cowley, D ;
Chinthammitr, Y ;
Robson, KJH ;
Townsend, ARM .
BLOOD, 2005, 105 (10) :4096-4102