Literature DB >> 8038893

Serum ferritin, blood donation, iron stores and haemochromatosis.

M Worwood1, C Darke.   

Abstract

Serum iron and ferritin concentrations were measured in 1,532 regular blood donors from South Wales who were undergoing HLA typing prior to registration on the British Bone Marrow and Platelet Donor Panel. Serum transferrin concentrations were determined for donors with serum iron concentrations > 24 mumol/l. There were 25 donors with transferrin saturations > 50% and 11 with transferrin saturations > 60%. There were five donors with serum ferritin concentrations > 200 micrograms/l (women) or > 300 micrograms/l (men). Two of the male donors had transferrin saturations > 50% and serum ferritin > 300 micrograms/l on repeat blood samples and are being treated by venesection. Donors with HLA-A3 did not differ from those without A3 in serum iron or ferritin concentrations. Even in the group of donors who were apparently homozygous for A3 there were neither abnormal serum iron nor ferritin concentrations. Although it is well established that measurements of transferrin saturation are required to detect homozygous haemochromatosis (HFE) in its earlier stages, the number of 'false-positive' results is likely to be unacceptably high for screening blood donors. Serum ferritin assays should identify donors with HFE and iron overload before the onset of liver damage. With two million regular donors and 300,000 new donors each year, a significant proportion of the U.K. population will be screened within 10 years. The assay of serum ferritin identifies donors with low levels of storage iron who are at risk of developing iron-deficiency anaemia. Furthermore, donation frequency may be increased for those donors with higher ferritin concentrations when blood supplies are low.

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Year:  1993        PMID: 8038893     DOI: 10.1111/j.1365-3148.1993.tb00100.x

Source DB:  PubMed          Journal:  Transfus Med        ISSN: 0958-7578            Impact factor:   2.019


  5 in total

1.  A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium.

Authors: 
Journal:  Gut       Date:  1997-12       Impact factor: 23.059

2.  Liver iron concentrations in sudden infant death syndrome.

Authors:  C A Moore; R Raha-Chowdhury; D G Fagan; M Worwood
Journal:  Arch Dis Child       Date:  1994-04       Impact factor: 3.791

3.  Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis.

Authors:  R Raha-Chowdhury; D J Bowen; A K Burnett; M Worwood
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

4.  Frequencies of the hereditary hemochromatosis allele in different populations. Comparison of previous phenotypic methods and novel genotypic methods.

Authors:  Nils Milman; Palle Pedersen; Torkil á Steig; Gitte Vedel Melsen
Journal:  Int J Hematol       Date:  2003-01       Impact factor: 2.490

5.  Postmortem blood ferritin concentrations in sudden infant death syndrome.

Authors:  M Worwood; R Raha-Chowdhury; D G Fagan; C A Moore
Journal:  J Clin Pathol       Date:  1995-08       Impact factor: 3.411

  5 in total

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