Distribution of transferrin saturations in the African-American population

被引:28
作者
Gordeuk, VR
McLaren, CE
Looker, AC
Hasselblad, V
Brittenham, GM
机构
[1] George Washington Univ, Med Ctr, Dept Med, Washington, DC 20037 USA
[2] Moorhead State Univ, Dept Math, Moorhead, MN 56560 USA
[3] Natl Ctr Hlth Stat, Nutr Stat Branch, Hyattsville, MD 20782 USA
[4] Duke Univ, Ctr Hlth Policy Res & Educ, Durham, NC USA
[5] Case Western Reserve Univ, Sch Med, Dept Med, Metrohlth Med Ctr, Cleveland, OH USA
关键词
D O I
10.1182/blood.V91.6.2175.2175_2175_2179
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine if transferrin saturations in African Americans may reflect the presence of a gene that influences iron metabolism, we analyzed the distribution of these values in 808 African Americans from the second National Health and Nutrition Survey. We tested for a mixture of three normal distributions consistent with population genetics for a major locus effect in which the proportion of normal homozygotes is p(2); of heterozygotes, 2pq; of affected homozygotes, q(2); and in which p+q = 1. Three subpopulations based on transferrin saturation were present (P < .0001) and the fit to a mixture of three normal distributions was good (P = .2). A proportion of .009 was included in a subpopulation with a mean +/- standard deviation transferrin saturation of 63.4% +/- 5.7% (postulated homozygotes for a gene that influences iron metabolism), while a proportion of .136 had an intermediate saturation of 38.0% +/- 5.7% (postulated heterozygotes) and .856 a saturation of 24.6% +/- 5.7% (postulated normal homozygotes), These proportions were consistent with population genetics because the sum of the square roots of the proportions with the lowest mean transferrin saturation (P = .925) and the highest (q = 0.093) was approximately 1 (1.018). The results are consistent with the presence in African Americans of a common locus that influences iron metabolism. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:2175 / 2179
页数:5
相关论文
共 31 条
[1]  
[Anonymous], LAB PROCEDURES USED
[2]   DIAGNOSIS OF IRON DEFICIENCY ANEMIA [J].
BAINTON, DF ;
FINCH, CA .
AMERICAN JOURNAL OF MEDICINE, 1964, 37 (01) :62-&
[3]   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
[4]  
BOTHWELL TH, 1964, AM J CLIN NUTR, V14, P47, DOI 10.1093/ajcn/14.1.47
[5]   STUDIES ON FREE ERYTHROCYTE PROTOPORPHYRIN, PLASMA IRON AND PLASMA COPPER IN NORMAL AND ANEMIC SUBJECTS [J].
CARTWRIGHT, GE ;
HUGULEY, CM ;
ASHENBRUCKER, H ;
FAY, J ;
WINTROBE, MM .
BLOOD, 1948, 3 (05) :501-525
[7]  
CHAKRABORTY R, 1992, AM J HUM GENET, V50, P145
[8]   SICKLE-CELL DISEASE AND HEMOCHROMATOSIS [J].
CONRAD, ME .
AMERICAN JOURNAL OF HEMATOLOGY, 1991, 38 (02) :150-152
[9]  
CRUMP KS, 1985, TOXICOLOGICAL RISK A, P188
[10]   MAXIMUM LIKELIHOOD FROM INCOMPLETE DATA VIA EM ALGORITHM [J].
DEMPSTER, AP ;
LAIRD, NM ;
RUBIN, DB .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-METHODOLOGICAL, 1977, 39 (01) :1-38