临床儿科杂志 ›› 2021, Vol. 39 ›› Issue (12): 923-.doi: 10.3969/j.issn.1000-3606.2021.12.010

• 综合报道 • 上一篇    下一篇

重组人生长激素替代治疗对矮身材儿童非对称性二甲基精氨酸水平的影响

梁祎 1,2, 刘晶 1, 冷丽娜 1,3, 宋婷婷 1,4, 霍佳慧 1,2, 马慧娟 1,2   

  1. 1 . 河北省人民医院代谢病重点实验室(河北石家庄 050000);2. 河北医科大学(河北石家庄 050000); 3 .河北北方学院(河北张家口 075000);4 .华北理工大学(河北唐山 063000)
  • 发布日期:2021-12-22
  • 通讯作者: 河北省医学适用技术跟踪项目(No.G2018004)
  • 基金资助:
    马慧娟 电子信箱:huijuanma 76 @ 163 .com

The effect of recombinant human growth hormone replacement therapy on the level of asymmetric dimethylarginine in short stature children

LIANG Yi 1,2 , LIU Jing1 , LENG Lina1,3 , SONG Tingting1,4 , HUO Jiahui1,2 , MA Huijuan1,2   

  1. 1 . Key Laboratory of Metabolic Disease, Hebei General Hospital, Shijiazhuang 050000 , Hebei, China; 2 . Hebei Medical University, Shijiazhuang 050000 , Hebei, China; 3 . Hebei North University, Zhangjiakou 075000 , Hebei, China; 4 . North China University of Science and Technology, Tangshan 063000 , Hebei, China
  • Published:2021-12-22

摘要: 目的 分析矮身材儿童重组人生长激素(rhGH)治疗前后血清非对称性二甲基精氨酸(ADMA)水平变化。方 法 选取生长激素缺乏症(GHD)或特发性身材矮小(ISS)的矮身材儿童63例,健康对照儿童27例为研究对象。观察矮 身材儿童治疗前ADMA水平,身高标准差积分(HtSDS)、血脂、葡萄糖代谢参数、动脉硬化指数(Ai)、胰岛素抵抗指数 (HOMA-IR)、定量胰岛素敏感性检测指数(QUICKI)等指标变化,并与rhGH治疗6个月和12个月以及健康儿童进行比较。 结果 GHD组30例、ISS组33例、对照组27例。治疗前GHD组LDL-C、ADMA高于对照组;GHD组、ISS组的Ai水平均 高于对照组,而IGF- 1水平均低于对照组,差异有统计学意义(P<0.05)。rhGH治疗6个月和12个月后,GHD和ISS患儿 的HtSDS均较治疗前升高,IGF-1水平均高于治疗前,差异有统计学意义(P

关键词: 生长激素缺乏症; 特发性身材矮小; 非对称性二甲基精氨酸; 重组人生长激素; 心血管疾病; 动脉粥样硬化

Abstract: Objective To analyze the changes of serum asymmetric dimethylarginine (ADMA) levels before and after recombinant human growth hormone (rhGH) treatment in short stature children. Methods A total of 63 short children with growth hormone deficiency (GHD) or idiopathic short stature (ISS) and 27 healthy controls were selected as subjects. The ADMA level, height standard deviation score (HtSDS), blood lipid, glucose metabolism parameters, atherogenic index (Ai), homeostatic model assessment for insulin resistance index (HOMA-IR), quantitative insulin sensitivity check index (QUICKI) and other indexes before treatment were observed. They were compared with the indexes 6 and 12 months after rhGH treatment as well as those of healthy children. Results There were 30 children in GHD group, 33 children in ISS group and 27 children in control group. Before treatment, The LDL-C and ADMA levels in GHD group were significantly higher than those in control group (P<0.05). The level of Ai in GHD and ISS groups was higher than that in control group, while the level of IGF-1 was lower than that in control group, the differences were statistically significant (P<0.05). After 6 and 12 months of rhGH treatment, the levels of HtSDS and IGF-1 in children with GHD and ISS were higher than those before treatment, and the differences were statistically significant (P before treatment (P<0.05). The ADMA level of ISS children 12 months after treatment was lower than that before and 6 months after treatment, and the differences were statistically significant (P<0 . 05 ). Conclusions The level of ADMA in children with GHD is significantly higher than that in healthy children, suggesting that the risk of atherosclerotic cardiovascular disease is increased in children with short stature, especially in children with GHD. The rhGH replacement therapy for 12 months can effectively reduce ADMA level and improve lipid profile in short stature children, which may reduce the risk of atherosclerotic cardiovascular disease to a certain extent.

Key words: growth hormone deficiency; idiopathic short stature; asymmetric dimethylarginine, recombinant human growth hormone; cardiovascular disease; arteriosclerosis