Reinehr Thomas, de Sousa Gideon, Wabitsch Martin
Vestische Hospital for Children and Adolescents, University of Witten/Herdecke, Datteln, Germany.
J Pediatr Endocrinol Metab. 2006 Sep;19(9):1133-40. doi: 10.1515/jpem.2006.19.9.1133.
IGF-I and androgens are postulated to accelerate skeletal maturation in obese children.
We studied weight status (BMI-SDS), height-SDS, IGF-I, cortisol, DHEA-S, and testosterone in 356 obese children (aged 4-15 years; 54% females) and correlated them to differences between bone age and chronological age (deltaBA-CA). Direct multivariate linear regression analyses were conducted for the dependent variable deltaBA-CA, including BMI, age, gender, pubertal stage, IGF-I-SDS, cortisol, DHEA-S, and testosterone as independent variables separately in prepubertal and pubertal girls, and prepubertal and pubertal boys.
Height-SDS (r = 0.52), IGF-I (r = 0.33), and IGF-I-SDS (r = 0.36) were significantly (p < 0.001) correlated to deltaBA-CA. In multiple regression analyses, BMI and IGF-I-SDS were significantly positively (p < 0.001) correlated to deltaBA-CA independently of gender and pubertal stage. Testosterone was significantly positively correlated to detaBA-CA only in prepubertal girls (p = 0.035).
Since IGF-I concentrations were positively associated to deltaBA-CA independently of pubertal stage and gender, we put forward the hypothesis that this hormone may contribute to acceleration of skeletal maturation in obese children.
胰岛素样生长因子-I(IGF-I)和雄激素被假定可加速肥胖儿童的骨骼成熟。
我们研究了356名肥胖儿童(4至15岁;54%为女性)的体重状况(BMI标准差分值)、身高标准差分值、IGF-I、皮质醇、硫酸脱氢表雄酮(DHEA-S)和睾酮,并将它们与骨龄和实际年龄之差(骨龄-实际年龄差值)进行关联分析。分别对青春期前和青春期的女孩以及青春期前和青春期的男孩进行直接多元线性回归分析,以骨龄-实际年龄差值作为因变量,将BMI、年龄、性别、青春期阶段、IGF-I标准差分值、皮质醇、DHEA-S和睾酮作为自变量。
身高标准差分值(r = 0.52)、IGF-I(r = 0.33)和IGF-I标准差分值(r = 0.36)与骨龄-实际年龄差值显著相关(p < 0.001)。在多元回归分析中,BMI和IGF-I标准差分值与骨龄-实际年龄差值显著正相关(p < 0.001),且不受性别和青春期阶段影响。睾酮仅在青春期前女孩中与骨龄-实际年龄差值显著正相关(p = 0.035)。
由于IGF-I浓度与骨龄-实际年龄差值呈正相关,且不受青春期阶段和性别的影响,我们提出假说,即这种激素可能促使肥胖儿童的骨骼成熟加速。