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血色素沉着症和铁过载筛查研究中白人和黑人的初始筛查转铁蛋白饱和度值、血清铁蛋白浓度及HFE基因型。

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in whites and blacks in the Hemochromatosis and Iron Overload Screening Study.

作者信息

Barton James C, Acton Ronald T, Dawkins Fitzroy W, Adams Paul C, Lovato Laura, Leiendecker-Foster Cathie, McLaren Christine E, Reboussin David M, Speechley Mark R, Gordeuk Victor R, McLaren Gordon D, Sholinsky Phyliss, Harris Emily L

机构信息

Southern Iron Disorders Center, Birmingham, Alabama 35209, USA.

出版信息

Genet Test. 2005 Fall;9(3):231-41. doi: 10.1089/gte.2005.9.231.

Abstract

We compared initial screening data of 44,082 white and 27,124 black Hemochromatosis and Iron Overload Screening (HEIRS) Study participants. Each underwent serum transferrin saturation (TfSat) and ferritin (SF) measurements without regard to fasting, and HFE C282Y and H63D genotyping. Elevated measurements were defined as: TfSat more than 50% (men), more than 45% (women); and SF more than 300 ng/ml (men), more than 200 ng/ml (women). Mean TfSat and percentages of participants with elevated TfSat were significantly greater in whites than in blacks. Mean SF and percentages of participants with elevated SF were significantly greater in blacks than in whites. TfSat and SF varied by gender and age in whites and blacks. Prevalences of genotypes that included either C282Y or H63D were significantly greater in whites than in blacks. The prevalence of elevated TfSat and SF plus genotypes C282Y/C282Y, C282Y/H63D, or H63D/H63D was 0.006 in whites and 0.0003 in blacks. Among whites with HFE C282Y homozygosity, 76.8% of men and 46.9% of women had elevated TfSat and SF values. Three black participants had HFE C282Y homozygosity; one had elevated TfSat and SF values. Possible explanations for differences in TfSat and SF in whites and blacks and pertinence to the detection of hemochromatosis, iron overload, and other disorders with similar phenotypes are discussed.

摘要

我们比较了44082名白人和27124名黑人血色素沉着症和铁过载筛查(HEIRS)研究参与者的初始筛查数据。每位参与者均接受了血清转铁蛋白饱和度(TfSat)和铁蛋白(SF)测量,测量时不考虑是否空腹,同时还进行了HFE C282Y和H63D基因分型。升高的测量值定义为:TfSat男性超过50%、女性超过45%;SF男性超过300 ng/ml、女性超过200 ng/ml。白人的平均TfSat以及TfSat升高的参与者百分比显著高于黑人。黑人的平均SF以及SF升高的参与者百分比显著高于白人。白人和黑人的TfSat和SF随性别和年龄而变化。包含C282Y或H63D的基因型患病率在白人中显著高于黑人。TfSat和SF升高加上C282Y/C282Y、C282Y/H63D或H63D/H63D基因型的患病率在白人中为0.006,在黑人中为0.0003。在HFE C282Y纯合子的白人中,76.8%的男性和46.9%的女性TfSat和SF值升高。三名黑人参与者为HFE C282Y纯合子;其中一人TfSat和SF值升高。本文讨论了白人和黑人TfSat和SF差异的可能解释以及与血色素沉着症、铁过载和其他具有相似表型的疾病检测的相关性。

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