首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >An examination of the effects of different doses of recombinant human growth hormone on children with growth hormone deficiency
【2h】

An examination of the effects of different doses of recombinant human growth hormone on children with growth hormone deficiency

机译:检查不同剂量的重组人生长激素对生长激素缺乏症儿童的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The aim of the present study was to examine the effects of different doses of recombinant human growth hormone (rhGH) on children with growth hormone deficiency (GHD) and on thyroid and glucose metabolism to identify more reasonable therapeutic doses of growth hormone (GH) for the treatment of this condition. In total, 60 prepubertal patients with GHD were randomly divided into the high-dose and low-dose groups (n=30 per group). The groups were treated with 0.1 or 0.05 U/kg for 6 months, respectively. The follow-up study focused on changes to the serum levels of insulin-like growth factor-1 (IGF-1), insulin-like growth factor binding protein (IGFBP)-3, blood glucose, thyroid hormone [triiodothyronine (T3) and its prohormone, thyroxine (T4), and thyroid stimulating hormone (TSH)] and the analysis of variance of the repeated data. Changes in the height, body weight and bone age of the high-dose group were greater than those of the low-dose group. After 6 months of treatment, the difference in height between the two groups was statistically significant (P<0.05). Glucose metabolism in the two groups was consistent, but there was a statistically significant difference in the fasting blood glucose (FBG) levels of the two groups after 6 months of treatment (P<0.05). Prior to treatment, the T3, T4 and TSH values (the thyroid function tests) in the two groups, especially for the value of T3 in high-dose group were varied. However, 6 months after treatment, statistically significant differences between the two groups (P<0.05) were identified. In conclusion, 0.1 U/kg of GH is beneficial to children with GHD in attaining a satisfactory height, but it leads to insulin resistance. Thus, glucose metabolism and thyroid function should be monitored on a regular basis in a clinical setting.
机译:本研究的目的是研究不同剂量的重组人生长激素(rhGH)对患有生长激素缺乏症(GHD)的儿童以及对甲状腺和葡萄糖代谢的影响,从而确定更合理的治疗剂量的生长激素(GH)。这种情况的治疗。共有60名GHD青春期前患者被随机分为高剂量组和低剂量组(每组n = 30)。各组分别用0.1或0.05 U / kg治疗6个月。后续研究的重点是血清中胰岛素样生长因子-1(IGF-1),胰岛素样生长因子结合蛋白(IGFBP)-3,血糖,甲状腺激素[三碘甲状腺素(T3)和它的激素,甲状腺素(T4)和甲状腺刺激激素(TSH)]以及重复数据的方差分析。高剂量组的身高,体重和骨龄的变化大于低剂量组。治疗6个月后,两组之间的身高差异具有统计学意义(P <0.05)。两组的葡萄糖代谢是一致的,但是治疗6个月后,两组的空腹血糖(FBG)水平存在统计学上的显着差异(P <0.05)。在治疗前,两组的T3,T4和TSH值(甲状腺功能检查),特别是大剂量组的T3值有所不同。但是,治疗后6个月,两组之间的差异有统计学意义(P <0.05)。总之,0.1 U / kg GH对GHD患儿达到令人满意的身高是有益的,但会导致胰岛素抵抗。因此,在临床环境中应定期监测葡萄糖代谢和甲状腺功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号