Department of Paediatrics and Endocrinology, Medical University of Warsaw, Poland.
Department of Laboratory Diagnostics and Clinical Immunology of Developmental Age, Medical University of Warsaw, 63A Żwirki i Wigury Street, 02-091 Warsaw, Poland.
Acta Biochim Pol. 2020 Nov 26;67(4):509-514. doi: 10.18388/abp.2020_5351.
The aim of the study was to investigate the influence of birth weight (BW), birth length (BL) and gestational age (GA) on growth pattern and metabolic profile in appropriate-for-gestational-age (AGA) growth hormone-deficient children before and during recombinant human growth hormone (rhGH) therapy. Forty children with isolated idiopathic growth hormone deficiency underwent auxological and biochemical assessment at baseline and after 6 and 12 months of rhGH therapy. Biochemical analysis included: insulin-like growth factor I (IGF-I), adiponectin, resistin, fasting glucose, fasting insulin, total cholesterol (total-C), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglycerides (TG) and glycated haemoglobin (HbA1c). There was a tendency for positive association between BW and baseline height standard deviation score (SDS). GA correlated with baseline weight SDS (p=0.019) and BMI SDS (p=0.039). GA was associated with baseline fasting glucose (p=0.031), fasting insulin (p=0.027), HOMA-IR (p=0.010) and QUICKI (p=0.016). BW correlated with baseline HbA1c (p=0.032). After the initiation of rhGH therapy we did not find any significant relationships between birth size parameters or GA and metabolic profile of the studied children. In conclusion, our results suggest that AGA GH-deficient children born with higher birth size parameters and higher GA had better first-year growth response to rhGH therapy and better baseline metabolic profile, especially parameters of carbohydrate metabolism. In order to optimize the effects of rhGH therapy, higher rhGH doses should be considered in those GH-deficient children who were born with lower birth size and GA.
本研究旨在探讨出生体重(BW)、出生长度(BL)和胎龄(GA)对生长激素缺乏症(GHD)儿童在接受重组人生长激素(rhGH)治疗前后生长模式和代谢特征的影响。40 名孤立性特发性 GHD 儿童在基线和 rhGH 治疗 6 个月和 12 个月时进行了人体测量学和生化评估。生化分析包括:胰岛素样生长因子 I(IGF-I)、脂联素、抵抗素、空腹血糖、空腹胰岛素、总胆固醇(总胆固醇)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、甘油三酯(TG)和糖化血红蛋白(HbA1c)。BW 与基线身高标准差评分(SDS)呈正相关趋势。GA 与基线体重 SDS(p=0.019)和 BMI SDS(p=0.039)相关。GA 与基线空腹血糖(p=0.031)、空腹胰岛素(p=0.027)、HOMA-IR(p=0.010)和 QUICKI(p=0.016)相关。BW 与基线 HbA1c 相关(p=0.032)。rhGH 治疗开始后,我们未发现出生大小参数或 GA 与研究儿童代谢特征之间存在任何显著关系。总之,我们的结果表明,出生时具有较高出生大小参数和较高 GA 的 AGA GHD 儿童对 rhGH 治疗的第一年生长反应更好,基线代谢特征更好,尤其是碳水化合物代谢参数。为了优化 rhGH 治疗效果,对于出生时出生大小和 GA 较低的 GHD 儿童,应考虑使用较高剂量的 rhGH。