重组生长激素治疗垂体功能减退1年。

K Takano, K Shizume, I Hibi, A Okuno, K Hanyu, S Suwa, H Nakajima, T Kondo, K Kato, N Iwatani
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引用次数: 0

摘要

25例垂体功能低下患者采用重组生长激素治疗1年,剂量为0.5 IU/kg/周。在先前未接受治疗的患者(n = 16)中,身高增加了4.5 - 10.2 cm,平均高度速度为7.7 +/- 1.8 cm/年(平均+/- SD)。在先前治疗的患者中(n = 9),身高增加3.9 - 7.6 cm,平均身高速度为5.8 +/- 1.0 cm/年,与先前垂体GH治疗期间观察到的相似。在两例患者中观察到低滴度的抗gh抗体。一名患者的抗体在治疗过程中消失。这些数据表明,重组生长激素具有促生长作用和低免疫原性。
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Treatment of hypopituitarism with recombinant somatropin for 1 year.

Twenty-five hypopituitary patients were treated with recombinant somatropin for 1 year at a dosage of 0.5 IU/kg/week. In previously untreated patients (n = 16), heights increased by between 4.5 and 10.2 cm, with a mean height velocity of 7.7 +/- 1.8 cm/year (mean +/- SD). In previously treated patients (n = 9), heights increased by between 3.9 and 7.6 cm, with a mean height velocity of 5.8 +/- 1.0 cm/year, similar to that observed during previous treatment with pituitary GH. Anti-GH antibodies were observed in two patients at a low titre. The antibodies disappeared in one patient during the treatment. These data indicate that recombinant somatropin has a growth promoting effect and low immunogenicity.

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11th International Symposium on Growth and Growth Disorders. Proceedings of a meeting, Stockholm, Sweden, 26-27 April 1991. 12th International Symposium on Growth and Growth Disorders. Geneva, 25-26 October 1991. The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement. Growth hormone treatment in short children with chronic renal failure and after renal transplantation: combined data from European clinical trials. The European Study Group. Growth response in prepubertal children with idiopathic growth hormone deficiency during the first two years of treatment with human growth hormone. Analysis of the Kabi Pharmacia International Growth Study.
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