Bladowska Joanna, Zak Teresa, Zimny Anna, Zacharzewska-Gondek Anna, Gondek Tomasz Maciej, Szewczyk Paweł, Noga Leszek, Noczyńska Anna, Sąsiadek Marek J
Department of General Radiology, Interventional Radiology and Neuroradiology, Wroclaw Medical University, Wroclaw, Poland.
Department of Endocrinology and Diabetology for Children and Adolescents, Wroclaw Medical University, Wroclaw, Poland.
Brain Dev. 2014 Oct;36(9):770-7. doi: 10.1016/j.braindev.2013.11.008. Epub 2013 Dec 18.
The pathogenesis of idiopathic growth hormone deficiency (GHD) in children, including possible cerebral metabolic alterations, remains unclear. The aim of the study was to evaluate metabolic changes within the normal appearing brain in children with GHD using MR spectroscopy (MRS) and to correlate MRS measurements with hormonal concentrations and with pituitary gland size.
Seventy children with GHD (mean age 7.8 yrs) and 11 healthy controls (mean age 8.4 yrs) were enrolled in the study. The MRS examinations were performed on a 1.5T scanner. Voxels were located in the posterior cingulate gyrus (PCG) and the left parietal white matter (PWM). The NAA/Cr, Cho/Cr and mI/Cr ratios were analyzed. The metabolite ratios, pituitary gland size and hormonal concentrations: growth hormone (GH) in two stimulation tests and GH during the night, as well as IGF-1 (insulin-like growth factor) and IGFBP3 (insulin-like growth factor-binding protein) levels were also correlated.
There was a significant (p < 0.05) decrease of the NAA/Cr ratios in PCG and PWM in children with GHD compared to the normal subjects. Other metabolite ratios showed no significant differences. We also found significant positive correlations between NAA/Cr ratio in PWM and IGFBP3 level, as well as with GH concentration in a stimulation test with glucagon.
The reduction of NAA/Cr ratios may suggest loss of neuronal activity within normal appearing gray and white matters in children with GHD. MRS could be a sensitive marker of cerebral metabolic disturbances associated with GHD and maybe used as an additional indicator for therapy with recombinant GH.
儿童特发性生长激素缺乏症(GHD)的发病机制,包括可能的脑代谢改变,仍不清楚。本研究的目的是使用磁共振波谱(MRS)评估GHD患儿外观正常脑内的代谢变化,并将MRS测量结果与激素浓度及垂体大小相关联。
70例GHD患儿(平均年龄7.8岁)和11例健康对照者(平均年龄8.4岁)纳入本研究。MRS检查在1.5T扫描仪上进行。体素位于后扣带回(PCG)和左侧顶叶白质(PWM)。分析NAA/Cr、Cho/Cr和mI/Cr比值。还对代谢物比值、垂体大小和激素浓度进行了关联分析,包括两次刺激试验中的生长激素(GH)、夜间GH、胰岛素样生长因子-1(IGF-1)和胰岛素样生长因子结合蛋白-3(IGFBP3)水平。
与正常受试者相比,GHD患儿PCG和PWM中的NAA/Cr比值显著降低(p<0.05)。其他代谢物比值无显著差异。我们还发现PWM中的NAA/Cr比值与IGFBP3水平以及与胰高血糖素刺激试验中的GH浓度之间存在显著正相关。
NAA/Cr比值降低可能提示GHD患儿外观正常的灰质和白质中神经元活动丧失。MRS可能是与GHD相关的脑代谢紊乱的敏感标志物,可作为重组GH治疗的额外指标。