Pinto G, Bussières L, Recasens C, Souberbielle J C, Zerah M, Brauner R
Department of Pediatric Endocrinology, Université René-Descartes and Hôpital Necker-Enfants Malades, Paris, France.
Horm Res. 2000;53(4):163-9. doi: 10.1159/000023562.
Patients operated on for craniopharyngioma frequently suffer from hyperphagia and are obese, but their statural growth is normal despite growth hormone (GH) deficiency. We have evaluated the hormonal factors influencing changes in weight and growth in 17 children before and 1, 3-6, 12, and/or 24 months after surgical resection of a craniopharyngioma performed at 7.7 +/- (SE) 1 years of age. Of these, 15 patients had a GH deficiency before surgery, and all had complete pituitary deficiency after it. The plasma fasting insulin concentrations before surgery were positively correlated with body mass index (BMI, kg/m(2); p < 0.05), plasma insulin-like growth factors (IGFI, p = 0.03, and IGFII, p = 0.04), and leptin (p = 0.03). They increased significantly 1 month after surgery and continued to increase thereafter, whereas leptin increased significantly only 3-6 months after surgery, paralleling changes in BMI. The plasma fasting insulin concentrations before surgery were also positively correlated with the weight changes (12.3 +/- 2.3 kg, p < 0.01) during the 12 months after surgery, but not with changes in BMI SDS (3.1 +/- 0.5, p = 0.07). Both expressions of weight change were correlated with the concomitant growth rates (4.8 +/- 0.7 cm, p < 0.01). IGFI was above the 10th percentile for children with idiopathic short stature in 10 of 15 patients with craniopharyngioma-induced GH deficiency and IGF-binding protein 3 in 14 of 15 patients. Craniopharyngioma itself modified the control of insulin secretion, and surgery increased the insulin secretion which continued in the same way in a given patient after surgery. The increased insulin secretion in turn increases weight and keeps IGFI nearly normal. This may explain the normal growth rate despite the complete lack of GH.
因颅咽管瘤接受手术的患者常出现食欲亢进和肥胖,但尽管生长激素(GH)缺乏,其身高增长仍正常。我们评估了17名儿童在7.7±(标准误)1岁时接受颅咽管瘤手术切除前、术后1、3 - 6、12和/或24个月影响体重和生长变化的激素因素。其中,15例患者术前存在GH缺乏,术后均出现完全性垂体功能减退。术前空腹血浆胰岛素浓度与体重指数(BMI,kg/m²;p < 0.05)、血浆胰岛素样生长因子(IGF - I,p = 0.03,IGF - II,p = 0.04)和瘦素(p = 0.03)呈正相关。术后1个月显著升高,此后持续升高,而瘦素仅在术后3 - 6个月显著升高,与BMI变化平行。术前空腹血浆胰岛素浓度也与术后12个月内的体重变化(12.3±2.3 kg,p < 0.01)呈正相关,但与BMI标准差评分变化(3.1±0.5,p = 0.07)无关。两种体重变化表达均与同期生长速率(4.8±0.7 cm,p < 0.01)相关。15例颅咽管瘤所致GH缺乏患者中有10例IGF - I高于特发性身材矮小儿童的第10百分位数,15例中有14例IGF结合蛋白3高于该标准。颅咽管瘤本身改变了胰岛素分泌的调控,手术增加了胰岛素分泌,术后在特定患者中以相同方式持续存在。胰岛素分泌增加进而增加体重并使IGF - I接近正常。这可能解释了尽管完全缺乏GH但生长速率仍正常的原因。