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Registration System for Growth Hormone (GH) Treatment With Standardized Immunoreactive GH Values in Japan

机译:日本具有标准免疫反应性GH值的生长激素(GH)治疗注册系统

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References(11) Cited-By(12) The Foundation for Growth Science has been controlling the use of GH by its registration system, which includes a scoring system for the eligibility for GH treatment according to the diagnostic criteria for GH deficiency (GHD) established by the Study Group for Hypothalamo-pituitary Disorder of the Ministry of Health and Welfare. Until 1995, 28, 876 patients with GHD (19, 432 boys and 9, 444 girls) had been registered as eligible for GH treatment. The number of patients registered in a year increased gradually till 1990 due to the unlimited hGH supply by recombinant techniques and the change in the criteria for GH treatment and the number registered became stable after 1990. The frequency of GH- treated patients is calculated to be 55.2/100, 000 persons (72.2/100, 000 in boys and 37.1/100, 000 in girls) in patients born between 1960 and 1990. The highest frequency was 148.4/100, 000 persons (191.7/ 100, 000 boys and 103.7/100, 000 girls) in 1981, when 2, 278 patients (1, 508 boys and 770 girls) were born. Eligibility for GH treatment is assessed according to the scoring system which is basically dependent on peak GH values in provocation tests so that standardization of GH values measured with the various commercial GH kits is required to avoid inequality of patients' access to the treatment. In samples obtained by GRF test in 10 normal volunteers, hGH was measured with seven human GH (hGH) kits at a laboratory center. Since the RIA value has been used historically for the diagnosis of GHD, the mean of two RIA measurements was selected as the basis for the standardization procedure and the linear regression formula was used for each hGH kit. After the freely available supply of hGH obtained by recombinant DNA techniques, the role of the Foundation for Growth Science has changed to avoid hGH abuse. Even with this regulation, the frequency of registered patients may indicate a tendency to GH overuse.
机译:参考文献(11)被引用(12)生长科学基金会一直在通过其注册系统来控制GH的使用,该系统包括根据已建立的GH缺乏症诊断标准(GHD)进行GH治疗资格评分系统由卫生和福利部下丘脑-垂体疾病研究小组负责。直到1995年,已有28,876名GHD患者(19,432名男孩和9,444名女孩)被登记为有资格接受GH治疗。由于重组技术提供无限量的hGH以及GH治疗标准的改变,直到1990年,一年中登记的患者人数逐渐增加,直到1990年。登记的GH治疗患者的频率为1960年至1990年出生的患者中,有55.2 / 100,000人(男生72.2 / 100,000,女孩中37.1 / 100,000女)。最高发生率是148.4 / 100,000人(191.7 / 100,000男和103.7 1981年有100,000名女孩出生,当时有2 278名患者(1,508名男孩和770名女孩)出生。根据评分系统评估GH治疗的资格,该评分系统主要取决于激发试验中的GH峰值,因此需要使用各种商用GH试剂盒测量的GH值标准化,以避免患者获得治疗的不平等。在10名正常志愿者中通过GRF测试获得的样品中,在实验室中心使用7种人类GH(hGH)试剂盒测量了hGH。由于RIA值在历史上一直用于诊断GHD,因此选择两次RIA测量的平均值作为标准化程序的基础,并对每个hGH试剂盒使用线性回归公式。通过重组DNA技术免费获得hGH后,生长科学基金会的作用发生了变化,从而避免了hGH的滥用。即使有此规定,注册患者的频率也可能表明GH过度使用的趋势。

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