hypothyroidism in β-thalassemia intermedia patients with and without hydroxyurea
نویسندگان
چکیده
hydroxyurea (hu) has been successfully used in patients with β-thalassemia intermedia (β-ti). we aimed to evaluate the effect of the long-term use of hu on thyroid function in patients with β-ti. seventy-five patients with β-ti aged≥11 years and taking hu were randomly selected during 2010 in southern iran. thirty-one patients with β-ti without hu were considered as a control group. serum levels of thyroid stimulating hormone (tsh) and t4 were measured. the mean age of the participants was 22.7±5.1 years (age range=12-41 years). serum ferritin level had no significant correlation with hu consumption (p>0.05). overall, we detected 10 (9.4%) patients with hypothyroidism. we found that the use of hu at a dose of 8-15 mg/kg/day has no significant association with thyroid function in β-ti patients. however, due to the small sample size in our study, documentation of this finding needs further studies with higher numbers of patients.
منابع مشابه
Hypothyroidism in β-Thalassemia Intermedia Patients with and without Hydroxyurea
Hydroxyurea (HU) has been successfully used in patients with β-thalassemia intermedia (β-TI). We aimed to evaluate the effect of the long-term use of HU on thyroid function in patients with β-TI. Seventy-five patients with β-TI aged≥11 years and taking HU were randomly selected during 2010 in southern Iran. Thirty-one patients with β-TI without HU were considered as a control group. Serum level...
متن کاملHypothyroidism in β-Thalassemia Intermedia Patients with and without Hydroxyurea
Hydroxyurea (HU) has been successfully used in patients with β-thalassemia intermedia (β-TI). We aimed to evaluate the effect of the long-term use of HU on thyroid function in patients with β-TI. Seventy-five patients with β-TI aged≥11 years and taking HU were randomly selected during 2010 in southern Iran. Thirty-one patients with β-TI without HU were considered as a control group. Serum level...
متن کاملSide effects of hydroxyurea in patients with Thalassemia major and thalassemia intermedia and sickle cell anemia
Background Sickle hemoglobin is the most common abnormal hemoglobin in the United States. Hemoglobin S arises as a result of a single amino acid substitution (glutamic acid to valin at position 6 of the β-globine chain). The presence of fetal hemoglobin (HbF) plays a relatively protective role since a significant amount of HbF interferes with HbS polymerization, the pathogenesis mechanism of ...
متن کاملfrequency of cholelithiasis in patients with beta-thalassemia intermedia with and without hydroxyurea
background recent studies regarding the effect of hydroxyurea (hu) in thalassemia have revealed favorable effects on the reduction of ineffective erythropoiesis. objectives the aim of the current study was to evaluate whether or not hu can have an effect on the gallstone formation rate in patients with beta-thalassemia intermedia (bti). patients and methods in this case control cross-sectional ...
متن کاملFrequency of Cholelithiasis in Patients With Beta-Thalassemia Intermedia With and Without Hydroxyurea
BACKGROUND Recent studies regarding the effect of hydroxyurea (HU) in thalassemia have revealed favorable effects on the reduction of ineffective erythropoiesis. OBJECTIVES The aim of the current study was to evaluate whether or not HU can have an effect on the gallstone formation rate in patients with beta-thalassemia intermedia (BTI). PATIENTS AND METHODS In this case control cross-sectio...
متن کاملSide effects of hydroxyurea in patients with Thalassemia major and thalassemia intermedia and sickle cell anemia
BACKGROUND Sickle hemoglobin is the most common abnormal hemoglobin in the United States. Hemoglobin S arises as a result of a single amino acid substitution (glutamic acid to valin at position 6 of the β-globine chain). The presence of fetal hemoglobin (HbF) plays a relatively protective role since a significant amount of HbF interferes with HbS polymerization, the pathogenesis mechanism of th...
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عنوان ژورنال:
iranian journal of medical sciencesجلد ۳۹، شماره ۱، صفحات ۶۰-۰
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