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慢性肾衰竭儿童的体内铁储备与HLA表型的关系

Body iron stores in children with chronic renal failure in relation to HLA phenotypes.

作者信息

Müller-Wiefel D E, Lenhard V, Schärer K

出版信息

Proc Eur Dial Transplant Assoc. 1981;18:524-30.

PMID:7329981
Abstract

In 57 children with chronic renal failure (19 on conservative treatment, 25 haemodialysis and 13 after transplantation) body iron stores were determined by an immunoradiometric assay with a heterologous antibody system in relation to haemochromatosis alleles, HLA A3 and B7. Iron overload, predominantly found during haemodialysis, depended on the number of erythrocyte transfusions given and was found to be more pronounced in patients with HLA A3 and/or B7. The frequency of these antigens was significantly higher in patients with iron overload (91%) than with normal (43%) or decreased (44%) iron stores. The relative risk of iron overload was calculated to be 2.0 for HLA A3 and 8.7 for HLA B7. The results suggest that erythrocyte transfusion therapy should be minimised in children with haemochromatosis alleles in order to avoid organ damage by haemosiderosis.

摘要

在57例慢性肾衰竭儿童中(19例接受保守治疗,25例接受血液透析,13例接受移植后),采用异源抗体系统的免疫放射分析方法,针对血色素沉着病等位基因HLA A3和B7测定体内铁储备。铁过载主要见于血液透析期间,取决于红细胞输注次数,且在HLA A3和/或B7患者中更为明显。这些抗原在铁过载患者中的频率(91%)显著高于铁储备正常(43%)或降低(44%)的患者。HLA A3的铁过载相对风险计算为2.0,HLA B7为8.7。结果表明,对于携带血色素沉着病等位基因的儿童,应尽量减少红细胞输血治疗,以避免含铁血黄素沉着症对器官造成损害。

相似文献

1
Body iron stores in children with chronic renal failure in relation to HLA phenotypes.慢性肾衰竭儿童的体内铁储备与HLA表型的关系
Proc Eur Dial Transplant Assoc. 1981;18:524-30.
2
HLA determinants in idiopathic haemochromatosis.特发性血色素沉着症中的人类白细胞抗原决定簇
Dan Med Bull. 1985 Oct;32(5):262-4.
3
Serum ferritin in haemodialysis patients: is there a relationship to 'haemochromatosis alleles' HLA A3, B7, B14?
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Serum ferritin in haemodialysis patients: role of blood transfusions and 'haemochromatosis alleles' HLA A3, B7 and B14.血液透析患者的血清铁蛋白:输血及“血色素沉着病等位基因” HLA A3、B7和B14的作用
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[Serum ferritin in children with disorders of iron balance].[铁平衡紊乱儿童的血清铁蛋白]
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引用本文的文献

1
A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association.一项针对609个标记血色素沉着症基因的HLA单倍型的研究:(1)该基因在HLA - A位点附近的定位以及定义杂合子群体所需的特征,(2)关于血色素沉着症与HLA关联潜在原因的假说。
Am J Hum Genet. 1987 Aug;41(2):89-105.
2
Diagnosis and treatment of iron overload in paediatric patients on chronic haemodialysis.慢性血液透析患儿铁过载的诊断与治疗
Pediatr Nephrol. 1988 Jul;2(3):303-8. doi: 10.1007/BF00858682.