Hypoparathyroidism in transfusion-dependent patients with β-thalassemia

被引:23
作者
Chern, JPS
Lin, KH
机构
[1] Tao Yuan Hosp, Dept Family Med, Dept Hlth, Tao Yuan, Taiwan
[2] Natl Taiwan Univ, Natl Taiwan Univ Hosp, Dept Pediat, Coll Med, Taipei 10016, Taiwan
关键词
chelation; hypocalcemia; hypoparathyroidism; iron overload; thalassemia; transfusion;
D O I
10.1097/00043426-200205000-00014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the prevalence of hypoparathyroidism in transfusion-dependent patients with beta-thalassemia. Patients and Methods: 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. Results: 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 mug/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. Conclusions: 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.
引用
收藏
页码:291 / 293
页数:3
相关论文
共 15 条
  • [1] COMBINED VITAMIN-D PARATHYROID DEFECT IN THALASSEMIA MAJOR
    ALOIA, JF
    OSTUNI, JA
    YEH, JK
    ZAINO, EC
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1982, 142 (04) : 831 - 832
  • [2] [Anonymous], 1925, Trans Am Pediatr Soc
  • [3] Survival and disease complications in thalassemia major
    Borgna-Pignatti, C
    Rugolotto, S
    De Stefano, P
    Piga, A
    Di Gregorio, F
    Gamberini, MR
    Sabato, V
    Melevendi, C
    Cappellini, MD
    Verlato, G
    [J]. COOLEYS ANEMIA: SEVENTH SYMPOSIUM, 1998, 850 : 227 - 231
  • [4] EFFICACY OF DEFEROXAMINE IN PREVENTING COMPLICATIONS OF IRON OVERLOAD IN PATIENTS WITH THALASSEMIA MAJOR
    BRITTENHAM, GM
    GRIFFITH, PM
    NIENHUIS, AW
    MCLAREN, CE
    YOUNG, NS
    TUCKER, EE
    ALLEN, CJ
    FARRELL, DE
    HARRIS, JW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (09) : 567 - 573
  • [5] Abnormal glucose tolerance in transfusion-dependent β-thalassemic patients
    Chern, JPS
    Lin, KH
    Lu, MY
    Lin, DT
    Lin, KS
    Chen, JD
    Fu, CC
    [J]. DIABETES CARE, 2001, 24 (05) : 850 - 854
  • [6] DESANCTIS V, 1992, ACTA HAEMATOL-BASEL, V88, P105
  • [7] DESANCTIS V, 1995, CLIN ENDOCRINOL, V42, P581
  • [8] Results of long-perm iron-chelating therapy
    Gabutti, V
    Piga, A
    [J]. ACTA HAEMATOLOGICA, 1996, 95 (01) : 26 - 36
  • [9] Giardini C, 1994, Curr Opin Hematol, V1, P170
  • [10] Iron-chelating therapy and the treatment of thalassemia
    Olivieri, NF
    Brittenham, GM
    [J]. BLOOD, 1997, 89 (03) : 739 - 761