Boguszewski M, Rosberg S, Albertsson-Wikland K
Department of Pediatrics, University of Goteborg, Sweden.
J Clin Endocrinol Metab. 1995 Sep;80(9):2599-606. doi: 10.1210/jcem.80.9.7673401.
To evaluate spontaneous GH secretion in terms of both secretory rate and pulsatile pattern in prepubertal children born small for gestational age (SGA) and still short (below -2 SD scores) at or after 2 yr of age, 24-h GH profiles were investigated in 106 such patients (75 boys and 31 girls; mean age, 7.3 +/- 0.3 yr), 14 of whom (10 boys and 4 girls) had Silver-Russell syndrome. The 24-h secretion of GH was compared with that in 2 reference populations of prepubertal children born at an appropriate size for gestational age (AGA): 179 short healthy children (143 boys and 36 girls; mean age, 10.2 +/- 0.2 yr) and 73 children of normal stature (54 boys and 19 girls; mean age, 10.4 +/- 0.3 yr). Plasma GH concentrations from the 24-h profiles were transformed to GH secretion rates by means of a deconvolution technique. For the SGA children, the mean GH secretion rate was 0.3 U/24 h, with a positive correlation with age, whereas for the reference groups it was higher, 0.5 U/24 h for the short children (P < 0.05) and 0.7 U/24 h for the children of normal stature (P < 0.001). Interestingly, the GH secretion rate correlated positively with weight for height, expressed as the SD score, in girls born SGA (r = 0.40; P < 0.05), whereas an inverse correlation was found for the short AGA girls (r = -0.44; P < 0.05). The mean baseline GH level in the SGA children correlated negatively with age (r = -0.53; P < 0.01), with the highest values found for children younger than 6 yr of age. On the average, 8 GH peaks/24-h period were found in all groups of children, and using Fourier time-series analyses, a similar rhythmicity was found in all groups. In the SGA group, the children younger than 6 yr of age had more GH peaks with lower amplitudes than the older children. It is concluded that children born SGA and still short at or after 2 yr of age spontaneously secrete less GH than healthy children of short stature born AGA. Both of these subgroups of prepubertal short children, however, secrete less GH than children of normal height. This finding might in part explain the growth failure in SGA children. Moreover, in the youngest SGA children (2-6 yr of age) there was another pattern of GH secretion, with a high basal GH level, a low peak amplitude, and a high peak frequency.(ABSTRACT TRUNCATED AT 400 WORDS)
为评估小于胎龄儿(SGA)出生的青春期前儿童在2岁及2岁以后仍身材矮小(低于-2标准差分数)时的生长激素(GH)自发分泌情况,包括分泌率和脉冲模式,我们对106例此类患者(75名男孩和31名女孩;平均年龄7.3±0.3岁)进行了24小时GH谱研究,其中14例(10名男孩和4名女孩)患有Silver-Russell综合征。将这些SGA儿童的24小时GH分泌情况与2组出生时为适于胎龄儿(AGA)的青春期前儿童参考人群进行比较:179名身材矮小的健康儿童(143名男孩和36名女孩;平均年龄10.2±0.2岁)和73名正常身高儿童(54名男孩和19名女孩;平均年龄10.4±0.3岁)。通过去卷积技术将24小时谱中的血浆GH浓度转换为GH分泌率。对于SGA儿童,平均GH分泌率为0.3 U/24小时,与年龄呈正相关,而对于参考组,该值较高,身材矮小儿童为0.5 U/24小时(P<0.05),正常身高儿童为0.7 U/24小时(P<0.001)。有趣的是,SGA出生的女孩中,GH分泌率与身高体重的标准差分数呈正相关(r=0.40;P<0.05),而身材矮小的AGA女孩则呈负相关(r=-0.44;P<0.05)。SGA儿童的平均基础GH水平与年龄呈负相关(r=-0.53;P<0.01),6岁以下儿童的值最高。所有儿童组平均每24小时发现8个GH峰值,通过傅里叶时间序列分析,所有组均发现类似的节律性。在SGA组中,6岁以下儿童的GH峰值比年龄较大的儿童更多但幅度更低。结论是,2岁及2岁以后仍身材矮小的SGA出生儿童自发分泌的GH比AGA出生的身材矮小健康儿童少。然而,这两个青春期前身材矮小儿童亚组分泌的GH均比正常身高儿童少。这一发现可能部分解释了SGA儿童的生长发育迟缓。此外,最年幼的SGA儿童(2至6岁)存在另一种GH分泌模式,基础GH水平高、峰值幅度低且峰值频率高。(摘要截短至400字)