Evaluation of body iron status in Italian carriers of beta-thalassemia trait

Citation
B. Nobili et al., Evaluation of body iron status in Italian carriers of beta-thalassemia trait, NUTR RES, 21(1-2), 2001, pp. 55-60
Citations number
16
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
NUTRITION RESEARCH
ISSN journal
02715317 → ACNP
Volume
21
Issue
1-2
Year of publication
2001
Pages
55 - 60
Database
ISI
SICI code
0271-5317(200101/02)21:1-2<55:EOBISI>2.0.ZU;2-3
Abstract
Iron deficiency is the most common single nutrient disorder in humans. Carr iers of beta -thalassemia have frequently been considered patients in whom iron deficiency difficulty may co-exist because dyserythropoiesis enhances enteric iron absorption. We studied 185 normal children and 146 heterozygou s children for beta -thalassemia. Furthermore, 51 normal men and 45 men wit h beta -thalassemia trait as well as 43 normal women of childbearing age an d 25 carriers of the same age were studied. Serum ferritin estimations were performed by RIA technique. No difference in iron deficiency prevalence wa s found among heterozygous children for beta -thalassemia compared to norma l children. The same was observed in adults. As for iron overload, the only statistically significant difference has been observed among men. Affected men tend to develop iron overload. Carriers of beta -thalassemia are world -wide with a high rate among people of Mediterranean ancestry and in some d eveloping countries. This condition concerns millions of people and, theref ore, physicians should be aware that iron deficiency might co-exist or deve lop in many of them. (C) 2001 Elsevier Science Inc. All rights reserved.