Heterozygous beta-thalassemia: Not infrequent in Mexico

Citation
Gj. Ruiz-arguelles et al., Heterozygous beta-thalassemia: Not infrequent in Mexico, ARCH MED R, 32(4), 2001, pp. 293-295
Citations number
15
Categorie Soggetti
Medical Research General Topics
Journal title
ARCHIVES OF MEDICAL RESEARCH
ISSN journal
01884409 → ACNP
Volume
32
Issue
4
Year of publication
2001
Pages
293 - 295
Database
ISI
SICI code
0188-4409(200107/08)32:4<293:HBNIIM>2.0.ZU;2-T
Abstract
Background. The prevalence of beta -thalassemia in Mexico is not known in d etail. Methods. Data of studies investigating abnormal hemoglobins between Septemb er 1987 and November 2000 were analyzed; in addition, data of red-blood-cel l indices and clinical features were analyzed in patients identified as car riers of beta -thalassemia. Results. In 1,639 prospective studies looking for abnormal hemoglobins, 429 disclosed some abnormality; of these, 319 cases displayed abnormally high levels of hemoglobin A2, thus consistent with the diagnosis of beta -thalas semia. This hemoglobin abnormality represented 74.2% of all abnormalities, both quantitative and qualitative, of the molecule of hemoglobin. There wer e 317 heterozygotes and only two homozygotes. We have previously shown that the most frequent cause of anemia as the iatrotropic condition in Mexican mestizos is iron deficiency. We found that iron deficiency is 11.5 times mo re frequent than beta -thalassemia and that the latter is 1.3 times more fr equent than macrocytic/megaloblastic anemia. Conclusions. beta -thalassemia should not be considered as infrequent in Me xico, and individuals with red blood cell microcytosis and/or hypochromia w ith or without anemia should be screened for thalassemia. (C) 2001 IMSS. Pu blished by Elsevier Science Inc.