Barton James C, Acton Ronald T, Lee Pauline L, West Carol
Southern Iron Disorders Center, G105, 2022 Brookwood Medical Center Drive, Birmingham, AL 35209, USA.
Blood Cells Mol Dis. 2007 Sep-Oct;39(2):206-11. doi: 10.1016/j.bcmd.2007.03.008. Epub 2007 May 9.
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 not significant. The aggregate Q248H frequencies in African-Americans and Native Africans differed significantly (0.0525 vs. 0.0946, respectively; p=0.0021). 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% CI: 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.
铁转运蛋白多态性SLC40A1 Q248H(第6外显子,cDNA 744G→T;谷氨酰胺248→组氨酸)见于有或无铁过载的撒哈拉以南非洲裔人群,且与血清铁蛋白浓度(SF)升高相关。然而,与Q248H相关的铁过载风险尚未明确。我们汇总了先前报道的非裔美国人和非洲原住民中Q248H等位基因频率估计值,并计算了缺乏HFE C282Y的受试者中与Q248H相关的铁过载风险。来自阿拉巴马州的两个队列以及华盛顿特区和加利福尼亚州各一个队列的1038名非裔美国人中,Q248H等位基因的总频率为0.0525(95%置信区间:0.0451,0.0652);这些队列中的频率无显著差异。来自东南非洲的两个队列中的259名原住民中,总频率为0.0946(95%置信区间:0.0694,0.1198);这些队列的频率差异不显著。非裔美国人和非洲原住民中Q248H的总频率有显著差异(分别为0.0525和0.0946;p = 0.0021)。有报道称,24名无HFE C282Y的非裔美国人和15名无HFE C282Y的非洲原住民存在铁过载。在非裔美国人中,使用610名未根据SF进行选择的C282Y阴性对照受试者,Q248H相关铁过载风险的比值比(OR)为1.57(95%置信区间:0.52,4.72;p = 0.29)。在非洲原住民中,使用208名未根据SF进行选择的对照受试者,OR为1.05(95%置信区间:0.28,3.90;p = 0.58)。我们得出结论,非裔美国人中SLC40A1 Q248H的频率显著低于非洲原住民。尽管有Q248H的非裔美国人和非洲原住民中铁过载的OR估计值大于1,但OR的增加无统计学意义。