l'Allemand Dagmar, Schmidt Stefan, Rousson Valentin, Brabant Georg, Gasser Theo, Grüters Annette
Children's Hospital, Charite Campus Virchow, Humboldt University, Berlin, Germany.
Eur J Endocrinol. 2002 Apr;146(4):537-43. doi: 10.1530/eje.0.1460537.
To explain why adrenal androgens rise with increasing adiposity during childhood, the role of body mass index (BMI), leptin and IGF-I was studied. We also tested whether these parameters contribute to inducing premature adrenarche (PA).
In a cross-sectional study, 26 prepubertal obese children were compared with a group of 26 prepubertal children of normal weight, and 30 children under observation for PA were compared with 30 healthy children, matched for gender, bone age and BMI.
Relative contributions of BMI standard deviation scores (SDS) and height SDS, as well as unbound leptin and IGF-I, to the levels of androgens, dehydroepiandrosterone sulfate (DHEAS) and Delta4-androstenedione (AD) were investigated by means of stepwise regression models. Logarithms of all hormones were standardised for age using residuals of a simple regression analysis, labelled by the suffix '(res)'.
In the obese children, height SDS, IGF-I(res,) DHEAS(res) (all P<0.05), leptin(res) (P<0.01), and AD(res) (P=0.07) were higher than in the controls, and covariates were correlated with each other (leptin(res) versus BMI SDS r=0.71, IGF-I(res) versus height SDS r=0.61). In the stepwise regression analysis of control and obese children, BMI SDS explained 26% and leptin(res) explained 12% of the variability of DHEAS(res), but this percentage remained at 26% when both variables were simultaneously introduced into the model. In contrast, IGF-I(res) and BMI SDS alone each accounted for 15% of the variability of AD, and their joint influence accumulated to explain 28% of the variability of AD(res). In PA, neither BMI SDS nor leptin(res) were correlated with the increased androgens.
Before the onset of gonadal activity in obese and control children, DHEAS levels, to some extent, are explained by BMI and leptin, while IGF-I in addition to BMI in part accounts for AD levels. Enhanced adrenal androgen secretion in children with PA, however, may be explained by parameters other than leptin or BMI.
为了解释儿童期肾上腺雄激素为何会随着肥胖程度增加而升高,对体重指数(BMI)、瘦素和胰岛素样生长因子-I(IGF-I)的作用进行了研究。我们还测试了这些参数是否会导致性早熟(PA)。
在一项横断面研究中,将26名青春期前肥胖儿童与26名青春期前正常体重儿童进行比较,并将30名接受PA观察的儿童与30名性别、骨龄和BMI相匹配的健康儿童进行比较。
通过逐步回归模型研究BMI标准差评分(SDS)和身高SDS以及游离瘦素和IGF-I对雄激素、硫酸脱氢表雄酮(DHEAS)和Δ4-雄烯二酮(AD)水平的相对贡献。所有激素的对数使用简单回归分析的残差按年龄进行标准化,后缀为“(res)”。
肥胖儿童的身高SDS、IGF-I(res)、DHEAS(res)(均P<0.05)、瘦素(res)(P<0.01)和AD(res)(P=0.07)高于对照组,且协变量之间相互关联(瘦素(res)与BMI SDS的r=0.71,IGF-I(res)与身高SDS的r=0.61)。在对照组和肥胖儿童的逐步回归分析中,BMI SDS解释了DHEAS(res)变异性的26%,瘦素(res)解释了12%,但当两个变量同时纳入模型时,该百分比仍为26%。相比之下,单独的IGF-I(res)和BMI SDS各自解释了AD变异性的15%,它们的联合影响累计解释了AD(res)变异性的28%。在PA组中,BMI SDS和瘦素(res)均与雄激素升高无关。
在肥胖儿童和对照儿童性腺活动开始之前,DHEAS水平在一定程度上由BMI和瘦素解释,而IGF-I除BMI外部分解释了AD水平。然而,PA儿童肾上腺雄激素分泌增加可能由瘦素或BMI以外的参数解释。