Önder Aşan, Aycan Zehra, Koca Cemile, Ergin Merve, Çetinkaya Semra, Ağladıoğlu Sebahat Yılmaz, Peltek Kendirci Havva Nur, Baş Veysel Nijat
Sami Ulus Gynecology and Obstetrics, Children Health and Diseases Training and Research Hospital, Pediatric Endocrinology Clinic, Ankara, Turkey. E-ma-il:
J Clin Res Pediatr Endocrinol. 2014;6(1):22-7. doi: 10.4274/Jcrpe.1182.
To investigate serum asymmetric dimethylarginine (ADMA) levels in children with isolated growth hormone deficiency (GHD) and to determine the effect of GH replacement therapy on these levels.
31 patients diagnosed with isolated GHD and 29 age-and sex-matched healthy children were enrolled in the study. Height, weight and waist circumference were measured in all subjects. Fasting serum insulin-like growth factor-1 (IGF-1), IGF binding protein-3, glucose, insulin and lipid levels were evaluated. Serum ADMA levels were assessed using the enzyme-linked immunosorbent assay technique. The same evaluations were repeated on the 3rd and 6th months of treatment in 28 of the GHD cases.
There were no significant differences in ADMA levels between the patient and control groups [0.513±0.130 (0.291-0.820) µmol/L vs. 0.573±0.199 (0.241-1.049) µmol/L]. There was a positive correlation between serum ADMA and HbA1c levels in the control group. In the GHD cases, ADMA levels negatively correlated with high-density lipoprotein levels and positively correlated with low-density lipoprotein levels. There was also a significant increase in ADMA levels in patients receiving GH therapy compared to pre-treatment levels [serum ADMA level, 1.075±0.133 (0.796-1.303) µmol/L at the 3rd month and 0.923±0.121 (0.695-1.159) µmol/L at the 6th month of treatment]. There was a negative correlation between ADMA levels and homeostasis model assessment of insulin resistance values at the 6th month evaluation. There were no relationships between ADMA levels and age, sex, or pubertal state either before or during the treatment.
Serum ADMA levels were found to be similar in patients with GHD and in healthy children. However, serum ADMA levels showed a significant increase in GHD patients following GH replacement therapy.
研究孤立性生长激素缺乏症(GHD)患儿的血清不对称二甲基精氨酸(ADMA)水平,并确定生长激素替代治疗对这些水平的影响。
31例诊断为孤立性GHD的患者和29例年龄及性别匹配的健康儿童纳入本研究。测量所有受试者的身高、体重和腰围。评估空腹血清胰岛素样生长因子-1(IGF-1)、IGF结合蛋白-3、血糖、胰岛素和血脂水平。采用酶联免疫吸附测定技术评估血清ADMA水平。28例GHD病例在治疗的第3个月和第6个月重复进行相同评估。
患者组和对照组的ADMA水平无显著差异[0.513±0.130(0.291 - 0.820)μmol/L对0.573±0.199(0.241 - 1.049)μmol/L]。对照组中血清ADMA与糖化血红蛋白水平呈正相关。在GHD病例中,ADMA水平与高密度脂蛋白水平呈负相关,与低密度脂蛋白水平呈正相关。与治疗前水平相比,接受生长激素治疗的患者ADMA水平也显著升高[治疗第3个月时血清ADMA水平为1.075±0.133(0.796 - 1.303)μmol/L,治疗第6个月时为0.923±0.121(0.695 - 1.159)μmol/L]。在第6个月评估时,ADMA水平与胰岛素抵抗稳态模型评估值呈负相关。治疗前及治疗期间,ADMA水平与年龄、性别或青春期状态均无关联。
发现GHD患者和健康儿童的血清ADMA水平相似。然而,生长激素替代治疗后,GHD患者的血清ADMA水平显著升高。