African iron overload

被引:56
作者
Gordeuk, VR [1 ]
机构
[1] Howard Univ, Dept Med, Ctr Sickle Cell Dis, Washington, DC 20059 USA
关键词
D O I
10.1053/shem.2002.35636
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Iron overload is common in rural sub-Saharan African populations that have the custom of drinking a traditional fermented beverage with high iron content. As with both excessive alcohol exposure and HFE hemochromatosis, hepatic portal fibrosis and micronodular cirrhosis are prominent sequelae of African iron overload. Two observations are therefore important in characterizing iron overload in Africa. First, the hepatic iron concentrations associated with African iron overload often far exceed those seen in alcoholic liver disease and histologic changes of alcohol effect are almost always absent. Second, the pattern of iron accumulation in African dietary iron is prominent in both macrophages and hepatic parenchymal cells; this pattern is in contrast to HFE homochromatosis, which is marked by predominantly parenchymal iron-loading. For a long time, it was thought that African iron overload was purely dietary in nature, that increased iron and alcohol in the diet could fully explain markedly elevated tissue iron levels sometimes seen with this condition. Recent studies of pedigrees suggest that, in addition to high dietary iron content, a genetic defect may also be implicated in iron overload in Africans. These studies indicate that the possible defect is different from mutations in the HFE gene frequently found in Caucasians with iron overload, but the putative gene has not been identified. Recent studies also indicate that non-HFE iron overload occurs in African-Americans, but the prevalence and possible genetic basis is yet to be determined. Copyright 2002, Elsevier Science (USA). All rights reserved.
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页码:263 / 269
页数:7
相关论文
共 58 条
[1]  
Bartholomew D, 2001, IND WEEK, V250, P27
[2]   IRON OVERLOAD IN AFRICAN-AMERICANS [J].
BARTON, JC ;
EDWARDS, CQ ;
BERTOLI, LF ;
SHROYER, TW ;
HUDSON, SL .
AMERICAN JOURNAL OF MEDICINE, 1995, 99 (06) :616-623
[3]   Inheritance of two HFE mutations in African Americans:: Cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency [J].
Barton, JC ;
Acton, RT .
GENETICS IN MEDICINE, 2001, 3 (04) :294-300
[4]   VALUE OF HEPATIC IRON MEASUREMENTS IN EARLY HEMOCHROMATOSIS AND DETERMINATION OF THE CRITICAL IRON LEVEL ASSOCIATED WITH FIBROSIS [J].
BASSETT, ML ;
HALLIDAY, JW ;
POWELL, LW .
HEPATOLOGY, 1986, 6 (01) :24-29
[5]   Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA [J].
Beutler, E ;
Felitti, VJ ;
Koziol, JA ;
Ho, NJ ;
Gelbart, T .
LANCET, 2002, 359 (9302) :211-218
[6]  
BOTHWELL TH, 1964, AM J CLIN NUTR, V14, P47, DOI 10.1093/ajcn/14.1.47
[7]  
BOTHWELL TH, 1960, ARCH PATHOL, V70, P279
[8]  
BOTHWELL TH, 1984, S AFR MED J, V65, P601
[9]  
BOTHWELL TH, 1965, ARCH PATHOL, V79, P163
[10]   SIDEROSIS IN BANTU - A COMPARISON OF INCIDENCE IN MALES AND FEMALES [J].
BOTHWELL, TH ;
ISAACSON, C .
BMJ-BRITISH MEDICAL JOURNAL, 1962, (5277) :522-+