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首页> 外文期刊>Clinics >Clonidine-stimulated growth hormone concentrations (cut-off values) measured by immunochemiluminescent assay (ICMA) in children and adolescents with short stature
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Clonidine-stimulated growth hormone concentrations (cut-off values) measured by immunochemiluminescent assay (ICMA) in children and adolescents with short stature

机译:通过免疫化学发光法(ICMA)在身材矮小的儿童和青少年中测定可乐定刺激的生长激素浓度(临界值)

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OBJECTIVES: To establish cut-off values for growth hormone concentrations using clonidine as a secretagogue and an immunochemiluminescent assay as the method of measurement and to analyze the response time as well as the influence of gender, nutritional status and pubertal stage. METHODS: A total of 225 tests were performed in 3 patient groups, categorized as group 1 (normal), group 2 (idiopathic short stature) and group 3 (growth hormone deficiency). Among the 199 disease-free individuals, 138 were prepubertal, and 61 were pubertal. Clonidine (0.1 mg/m 2 ) was orally administered, and the growth hormone level was measured by immunochemiluminescent assay. The growth hormone peak and the difference between the growth hormone peak and the baseline level were then analyzed. Statistical analyses were performed using Studenta??s t-test or the Mann-Whitney test and Kruskal-Wallis test followed by Dunna??s post hoc test. Cut-off values were determined using a receiver operating characteristic curve. RESULTS: Group 1 and group 2 had no difference in growth hormone peak, gender, body mass index standard deviation score, or pubertal stage. Group 3 exhibited a significantly lower growth hormone peak than the other groups did. The receiver operating characteristic curve demonstrated that growth hormone concentrations a?¥ 3.0 ng/mL defined responsiveness to clonidine. In total, 3.02% of individuals in group 1 and group 2 were considered false positive, i.e., these children lacked growth hormone deficiency and had a peak below 3.0 ng/mL. CONCLUSION: Clonidine-stimulated growth hormone concentrations a?¥3 ng/mL, as measured by immunochemiluminescent assay, suggest responsiveness to the stimulus regardless of gender, body mass index standard deviation score or pubertal stage.
机译:目的:以可乐定作为促分泌素和免疫化学发光法作为测量方法,确定生长激素浓度的临界值,并分析其响应时间以及性别,营养状况和青春期的影响。方法:在3个患者组中共进行了225次测试,分为1组(正常),2组(特发性矮小)和3组(生长激素缺乏)。在199名无病个体中,青春期前为138名,青春期为61名。口服可乐定(0.1 mg / m 2),并通过免疫化学发光测定法测量生长激素水平。然后分析生长激素峰以及生长激素峰与基线水平之间的差异。统计分析使用Studenta的t检验或Mann-Whitney检验和Kruskal-Wallis检验,随后是Dunna的事后检验。临界值使用接收器工作特性曲线确定。结果:第1组和第2组在生长激素峰值,性别,体重指数标准差评分或青春期方面无差异。第3组的生长激素峰值明显低于其他各组。接受者的工作特征曲线表明,生长激素浓度≥3.0ng / mL确定了对可乐定的反应性。总的来说,第1组和第2组中有3.02%的人被认为是假阳性,即这些儿童缺乏生长激素缺乏症,并且峰值低于3.0 ng / mL。结论:通过免疫化学发光法测定可乐定刺激的生长激素浓度a?¥ 3 ng / mL,表明对刺激的反应性,无论性别,体重指数标准差评分或青春期如何。

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