海西定
TMPRSS6
医学
红细胞生成
缺铁
突变
内科学
基因
内分泌学
免疫学
贫血
生物化学
生物
酶
蛋白酶
丝氨酸蛋白酶
作者
M. L. H. Cuijpers,Erwin T. Wiegerinck,Rick Brouwer,T.J.M. de Witte,Dorine W. Swinkels
摘要
A 36-year old female patient who had had iron deficiency anaemia since her childhood showed no clear response to oral iron treatment. Elevated serum hepcidin levels were found after excluding other causes of iron deficiency. This is in contrast to what is expected in iron deficiency anaemia and indicates a primary defect in hepcidin regulation. Indeed, in the search for a defect in genes coding for hepcidin-regulating proteins the patient was found to be compound heterozygous for two different mutations in the TMPRSS6 gene. This leads to a dysfunctional matriptase-2 protein for which the gene codes. Consequently, liver cells cannot inhibit hepcidin production in the presence of low serum iron levels. High hepcidin levels result in less iron being absorbed from the bowel than is necessary for erythropoiesis. Therefore, patients with matriptase-2 deficiency respond poorly to oral iron treatment and have to be treated with intravenous iron.
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