Tanaka T
Endocrine Research Laboratory, National Children's Medical Centre, Tokyo, Japan.
Acta Paediatr Scand Suppl. 1991;379:126-35. doi: 10.1111/j.1651-2227.1991.tb12063.x.
Data for a total of 942 new cases of hypopituitarism, out of 3493 patients treated with recombinant human growth hormone (GH) for more than 1 year, have been analysed. The mean peak GH correlated well with clinical variables related to growth and was considered to be a good index of GH secretory capacity. Mean peak GH was correlated inversely with obesity (r = -0.253, p less than 0.01). The lower the height velocity before treatment, the mean peak GH and the height SDS, the greater was the therapeutic effect achieved. The patients with mean peak GH less than or equal to 5 ng/ml were defined as having complete GH deficiency (GHD), and those with a mean peak GH of 5-10 ng/ml as having partial GHD. The clinical entity of GH neurosecretory dysfunction could not be identified from either the clinical variables examined or the therapeutic effect. The appearance of GH antibody was considered to be of no clinical significance because its incidence and titre were both low.
对3493例接受重组人生长激素(GH)治疗超过1年的患者中的942例垂体功能减退新病例的数据进行了分析。平均GH峰值与生长相关的临床变量密切相关,被认为是GH分泌能力的良好指标。平均GH峰值与肥胖呈负相关(r = -0.253,p < 0.01)。治疗前身高增长速度、平均GH峰值和身高标准差评分越低,所取得的治疗效果越好。平均GH峰值小于或等于5 ng/ml的患者被定义为完全性GH缺乏(GHD),平均GH峰值为5 - 10 ng/ml的患者为部分性GHD。从所检查的临床变量或治疗效果中均无法识别出GH神经分泌功能障碍的临床实体。GH抗体的出现被认为无临床意义,因为其发生率和滴度均较低。