Hypoparathyroidism in Transfusion-Dependent Patients With β-Thalassemia
- 1 May 2002
- journal article
- Published by Wolters Kluwer Health in Journal of Pediatric Hematology/Oncology
- Vol. 24 (4) , 291-293
- https://doi.org/10.1097/00043426-200205000-00014
Abstract
To determine the prevalence of hypoparathyroidism in transfusion-dependent patients with beta-thalassemia. A total of 28 transfusion-dependent patients with beta-thalassemia were interviewed, and their serum calcium, phosphate, magnesium, and intact parathyroid hormone levels were checked. Serum ferritin levels were measured to monitor the effect of chelation therapy. Blood urea nitrogen, creatinine, total protein, and albumin were measured in patients with undetectable or low intact parathyroid hormone levels. The prevalence of hypoparathyroidism was 10.7% (3/28). Mean age at diagnosis was 18 years. The serum ferritin levels of patients with hypoparathyroidism were 1,032, 2,102, and 7,680 microg/L. Only one patient had clinical symptoms of hypocalcemia. All three of the patients with hypoparathyroidism had hypogonadism, and 66.7% (2/3) of the patients had insulin-dependent diabetes mellitus. Hypoparathyroidism in transfusion-dependent patients with beta-thalassemia seems to be accompanied by other endocrinopathies. Serum ferritin may not have been a reliable indicator of iron overload in the three patients with hypoparathyroidism. Severe iron overload would easily explain these multiple endocrinopathies. This pattern is commonly seen in iron-overloaded patients with thalassemia elsewhere.Keywords
This publication has 11 references indexed in Scilit:
- The β-ThalassemiasNew England Journal of Medicine, 1999
- Survival and Disease Complications in Thalassemia MajorAnnals of the New York Academy of Sciences, 1998
- Results of Long-Term Iron-Chelating TherapyActa Haematologica, 1996
- Multicentre study on prevalence of endocrine complications in thalassaemia majorClinical Endocrinology, 1995
- Efficacy of Deferoxamine in Preventing Complications of Iron Overload in Patients with Thalassemia MajorNew England Journal of Medicine, 1994
- Survival in Medically Treated Patients with Homozygous β-ThalassemiaNew England Journal of Medicine, 1994
- Hypoparathyroidism in Beta-Thalassemia majorActa Haematologica, 1992
- SURVIVAL AND CAUSES OF DEATH IN THALASSAEMIA MAJORPublished by Elsevier ,1989
- Combined vitamin D parathyroid defect in thalassemia majorArchives of internal medicine (1960), 1982
- The Spectrum of Hypoparathyroidism1Journal of Clinical Endocrinology & Metabolism, 1972