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血色素沉着症和铁过载筛查(HEIRS)研究中亚洲人、非裔美国人、西班牙裔和白人的转铁蛋白饱和度和血清铁蛋白浓度的双变量混合模型。

Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

作者信息

McLaren Christine E, Gordeuk Victor R, Chen Wen-Pin, Barton James C, Acton Ronald T, Speechley Mark, Castro Oswaldo, Adams Paul C, Snively Beverly M, Harris Emily L, Reboussin David M, McLachlan Geoffrey J, Bean Richard

机构信息

Department of Epidemiology, University of California, Irvine, California, USA.

出版信息

Transl Res. 2008 Feb;151(2):97-109. doi: 10.1016/j.trsl.2007.10.002. Epub 2007 Nov 9.

Abstract

Bivariate mixture modeling was used to analyze joint population distributions of transferrin saturation (TS) and serum ferritin concentration (SF) measured in the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Four components (C1, C2, C3, and C4) with successively age-adjusted increasing means for TS and SF were identified in data from 26,832 African Americans, 12,620 Asians, 12,264 Hispanics, and 43,254 whites. The largest component, C2, had normal mean TS (21% to 26% for women, 29% to 30% for men) and SF (43-82 microg/L for women, 165-242 microg/L for men), which consisted of component proportions greater than 0.59 for women and greater than 0.68 for men. C3 and C4 had progressively greater mean values for TS and SF with progressively lesser component proportions. C1 had mean TS values less than 16% for women (<20% for men) and SF values less than 28 microg/L for women (<47 microg/L for men). Compared with C2, adjusted odds of iron deficiency were significantly greater in C1 (14.9-47.5 for women, 60.6-3530 for men), adjusted odds of liver disease were significantly greater in C3 and C4 for African-American women and all men, and adjusted odds of any HFE mutation were increased in C3 (1.4-1.8 for women, 1.2-1.9 for men) and in C4 for Hispanic and white women (1.5 and 5.2, respectively) and men (2.8 and 4.7, respectively). Joint mixture modeling identifies a component with lesser SF and TS at risk for iron deficiency and 2 components with greater SF and TS at risk for liver disease or HFE mutations. This approach can identify populations in which hereditary or acquired factors influence metabolism measurement.

摘要

采用双变量混合模型分析在血色素沉着症和铁过载筛查(HEIRS)研究中测得的转铁蛋白饱和度(TS)和血清铁蛋白浓度(SF)的联合总体分布。在26,832名非裔美国人、12,620名亚洲人、12,264名西班牙裔和43,254名白人的数据中,识别出四个成分(C1、C2、C3和C4),其TS和SF的均值随年龄调整后依次增加。最大的成分C2,其TS均值正常(女性为21%至26%,男性为29%至30%),SF均值正常(女性为43 - 82μg/L,男性为165 - 242μg/L),女性的成分比例大于0.59,男性的成分比例大于0.68。C3和C4的TS和SF均值逐渐增大,成分比例逐渐减小。C1中女性的TS均值小于16%(男性小于20%),女性的SF均值小于28μg/L(男性小于47μg/L)。与C2相比,C1中铁缺乏的校正比值显著更高(女性为14.9 - 47.5,男性为60.6 - 3530),非裔美国女性和所有男性中,C3和C4中肝病的校正比值显著更高,C3中任何HFE突变的校正比值增加(女性为1.4 - 1.8,男性为1.2 - 1.9),西班牙裔和白人女性(分别为1.5和5.2)以及男性(分别为2.8和4.7)的C4中任何HFE突变的校正比值增加。联合混合模型识别出一个SF和TS较低且有缺铁风险的成分,以及两个SF和TS较高且有肝病或HFE突变风险的成分。这种方法可以识别出遗传或后天因素影响代谢测量的人群。

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