Völkl Thomas M K, Schwöbel Katja, Simm Diemud, Beier Christoph, Rohrer Tilman R, Dörr Helmuth G
Division of Pediatric Endocrinology, Hospital for Children and Adolescents, Friedrich-Alexander-University of Erlangen-Nuremberg, Loschgestrasse 15, 91054 Erlangen, Germany.
Growth Horm IGF Res. 2004 Dec;14(6):455-61. doi: 10.1016/j.ghir.2004.08.002.
To analyze spontaneous nocturnal GH profiles, IGF1 and IGFBP3 serum levels, as well as IGF1:IGFBP3 molar ratios in SGA children without postnatal catch-up growth.
Short statured prepubertal SGA children (n = 24) were matched retrospectively for sex, age and BMI to short statured children born appropriate for gestational age (AGA), who underwent the same diagnostic program. GH deficiency was excluded in all children by a normal increase of GH in 2 stimulation tests (>8 microg/L). For assessment of spontaneous nocturnal GH secretion, GH serum levels were measured every 20 min for 10 h. Pulsatility was analyzed with Pulsar.
None of the Pulsar derived descriptive parameters showed a significant difference between SGA and AGA children. Overall, median IGF1 levels were approximately one SDS below zero SDS (p < 0.001), whereas IGFBP3 levels were normal in both groups. Thus, the IGF1:IGFBP3 molar ratios were significantly lower from zero (p < 0.01) in SGA as well as in AGA children. However, IGF1- and IGFBP3-SDS levels related either to chronological or to bone age did not differ significantly between SGA and AGA children.
Building matched pairs of short statured children born either SGA or AGA for sex, age and BMI we did not find any significant differences in spontaneous nocturnal GH secretion, IGF1, IGFBP3, and IGF1:IGFBP3 molar ratios.
分析出生后无追赶生长的小于胎龄儿(SGA)儿童的夜间自发性生长激素(GH)谱、胰岛素样生长因子1(IGF1)和胰岛素样生长因子结合蛋白3(IGFBP3)血清水平,以及IGF1:IGFBP3摩尔比。
对青春期前身材矮小的SGA儿童(n = 24)进行回顾性匹配,根据性别、年龄和体重指数(BMI)与适于胎龄儿(AGA)出生的身材矮小儿童进行匹配,这些AGA儿童接受了相同的诊断程序。通过2次刺激试验中GH正常升高(>8μg/L)排除所有儿童的GH缺乏。为评估夜间自发性GH分泌,每20分钟测量10小时的GH血清水平。使用Pulsar分析脉冲性。
Pulsar得出的描述性参数在SGA和AGA儿童之间均未显示出显著差异。总体而言,IGF1水平中位数比标准差评分(SDS)低于零SDS约1个单位(p < 0.001),而两组中IGFBP3水平均正常。因此,SGA和AGA儿童的IGF1:IGFBP3摩尔比均显著低于零(p < 0.01)。然而,SGA和AGA儿童中按实际年龄或骨龄计算的IGF1和IGFBP3-SDS水平无显著差异。
构建按性别、年龄和BMI匹配的SGA或AGA出生的身材矮小儿童对,我们未发现夜间自发性GH分泌、IGF1、IGFBP3和IGF1:IGFBP3摩尔比有任何显著差异。