Abstract |
In thalassemia erythrocyte cation permeability is increased, but the increment in ATPase-dependent cation pumps maintains normal concentrations of Ca++, Na+ and K+. In this study we investigated erythrocyte concentrations of Mg++ in heterozygous beta-thalassemia and in microcytic sideropenic anemia. Twenty-five healthy controls, 40 heterozygous beta-thalassemics and 25 patients with sideropenic anemia were studied. Erythrocyte Mg++ was assayed either by atomic absorption or by standard laboratory methods. Erythrocyte Mg++ was significantly lower in the beta-thalassemia group than in the other two groups (p less than 0.001). Serum magnesium was significantly lower in sideropenic anemia patients than in beta-thalassemics and in controls (p less than 0.01), whereas these latter two groups showed similar values. Our results suggest that the increment in ATPase-dependent cation pumps is not sufficient to maintain normal erythrocyte Mg++ concentrations in heterozygous beta-thalassemia. In sideropenic anemia cation permeability is not increased, therefore erythrocyte Mg++ is normal. Low serum Mg++ levels in sideropenic anemia could be explained by a primary Mg++ deficit associated with sideropenia.
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Authors | V Abbasciano, G Bader, L Graziano, D Mazzotta, G Vecchiatti, C Guglielmini, S Sartori |
Journal | Haematologica
(Haematologica)
1991 Jul-Aug
Vol. 76
Issue 4
Pg. 339-41
ISSN: 0390-6078 [Print] Italy |
PMID | 1665466
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adolescent
- Adult
- Aged
- Anemia, Hypochromic
(blood, etiology)
- Cell Membrane Permeability
- Erythrocyte Membrane
(metabolism)
- Erythrocytes, Abnormal
(chemistry)
- Female
- Hemorrhage
(complications)
- Heterozygote
- Humans
- Ion Pumps
- Magnesium
(blood)
- Male
- Middle Aged
- Thalassemia
(blood, genetics)
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