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长效生长抑素类似物索马杜林在肢端肥大症中的药代动力学及疗效

Pharmacokinetics and efficacy of the long-acting somatostatin analogue somatuline in acromegaly.

作者信息

Johnson M R, Chowdrey H S, Thomas F, Grint C, Lightman S L

机构信息

Department of Medicine, Bristol Royal Infirmary, UK.

出版信息

Eur J Endocrinol. 1994 Mar;130(3):229-34. doi: 10.1530/eje.0.1300229.

DOI:10.1530/eje.0.1300229
PMID:7908838
Abstract

The aim of this work was to assess the use of a sustained-release formulation of somatuline, a long-acting analogue of somatostatin, in the treatment of acromegaly. Fifteen patients with active acromegaly, as defined by random growth hormone (GH) levels greater than 10 mU/l, which fail to be suppressed to less than 5 mU/l following an oral glucose load, were studied. Somatuline was administered as an intramuscular injection in two regimens: eight patients were given a single injection of the sustained-release formulation and blood samples taken over the next month for the measurement of both basal levels of GH and the GH response to thyrotrophin-releasing hormone; and eight patients were given injections of the sustained-release formulation at 2-week intervals over a 6-month period and basal plasma GH levels and the GH response to both an oral glucose load and to thyrotrophin-releasing hormone was assessed. Following a single intramuscular dose of the sustained-release preparation, random GH levels were reduced to below 10 mU/l in five patients and by greater than 50% of basal levels in the remainder. The insulin-like growth factor I (IGF-I) levels fell to within the normal range in three patients. In the long-term efficacy study. GH levels were reduced to < 10 mU/l in 7/8 patients. The IGF-I levels were normalized in four patients. Five of the eight patients experienced diarrhoea, two of mild and three of moderate severity; none of the patients withdrew from the study.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

这项研究的目的是评估生长抑素长效类似物索马杜林的缓释制剂在肢端肥大症治疗中的应用。研究对象为15例活动期肢端肥大症患者,其随机生长激素(GH)水平大于10 mU/l,口服葡萄糖负荷后未能被抑制至低于5 mU/l。索马杜林通过两种方案进行肌肉注射:8例患者单次注射缓释制剂,并在接下来的一个月内采集血样以测量基础GH水平以及GH对促甲状腺激素释放激素的反应;另外8例患者在6个月内每隔2周注射一次缓释制剂,并评估基础血浆GH水平以及GH对口服葡萄糖负荷和促甲状腺激素释放激素的反应。单次肌肉注射缓释制剂后,5例患者的随机GH水平降至10 mU/l以下,其余患者的GH水平降低超过基础水平的50%。3例患者的胰岛素样生长因子I(IGF-I)水平降至正常范围。在长期疗效研究中,8例患者中有7例的GH水平降至<10 mU/l。4例患者的IGF-I水平恢复正常。8例患者中有5例出现腹泻,2例为轻度,3例为中度;无患者退出研究。(摘要截断于250字)

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