Thibault H, Souberbielle J C, Taieb C, Brauner R
Paediatric Endocrinology Unit, Hôpital et Faculté Necker Enfants Malades, Paris, France.
Horm Res. 1993;40(4):136-40. doi: 10.1159/000183782.
The hypothesis that insufficient body weight is partly responsible for idiopathic short stature was tested by evaluating 79 prepubertal children having idiopathic short stature, classified according to their body mass index (BMI) zs: group 1 BMI zs < or = 0 (m +/- SE, -0.9 +/- 0.1, n = 53) and group 2 BMI zs > 0 (0.6 +/- 0.1, n = 26). Their ages were similar (8.1 +/- 0.3 and 8.4 +/- 0.4 years). The following parameters were significantly lower in group 1 than in group 2: height (-2.5 +/- 0.1 vs. -2.2 +/- 0.1 SD, p < 0.05), height velocity (-1.5 +/- 0.2 vs. -0.9 +/- 0.4 SD, p < 0.05), bone age (bone age retardation 2.3 +/- 0.2 vs. 1.3 +/- 0.4 years, p < 0.005) and plasma insulin-like growth factor 1 (IGF-1, 0.8 +/- 0.1 vs. 1.2 +/- 0.1 U/ml, p < 0.05). The BMI was significantly lower in children with idiopathic short stature (-0.4 +/- 0.1) than in the normal population (zs, p < 0.0002). BMI zs was positively correlated with height (p < 0.005), height velocity (p < 0.05) and plasma IGF-1 (p < 0.01). We conclude that children with idiopathic short stature are leaner than the normal population. An inadequate or insufficient nutritional intake may be partly responsible for idiopathic short stature. The effects of improved intake on the height change are under evaluation.
通过评估79名青春期前特发性矮小儿童来检验体重不足部分导致特发性矮小这一假设,这些儿童根据其体重指数(BMI)Z评分进行分类:第1组BMI Z评分≤0(均值±标准误,-0.9±0.1,n = 53),第2组BMI Z评分>0(0.6±0.1,n = 26)。两组儿童年龄相似(分别为8.1±0.3岁和8.4±0.4岁)。第1组以下参数显著低于第2组:身高(-2.5±0.1 vs. -2.2±0.1标准差,p<0.05)、身高增长速度(-1.5±0.2 vs. -0.9±0.4标准差,p<0.05)、骨龄(骨龄延迟2.3±0.2岁 vs. 1.3±0.4岁,p<0.005)以及血浆胰岛素样生长因子1(IGF-1,0.8±0.1 vs. 1.2±0.1 U/ml,p<0.05)。特发性矮小儿童的BMI显著低于正常人群(Z评分,p<0.0002)。BMI Z评分与身高(p<0.005)、身高增长速度(p<0.05)和血浆IGF-1(p<0.01)呈正相关。我们得出结论,特发性矮小儿童比正常人群更瘦。营养摄入不足或不充分可能部分导致特发性矮小。改善营养摄入对身高变化的影响正在评估中。