Department of Pediatric Diabetes, Auxology and Obesity, Institute of Pediatrics, Poznan University of Medical Sciences, 60-572 Poznan, Poland.
Doctoral School, Poznan University of Medical Sciences, 60-812 Poznan, Poland.
Nutrients. 2023 Apr 1;15(7):1734. doi: 10.3390/nu15071734.
Obesity in childhood is associated with several steroid changes, which result from excess body mass. The aim of this study was to evaluate steroid metabolism in children with obesity compared with those with normal weight, especially in relation to sex and puberty progress. We analyzed the clinical data of 191 children, aged between 5 and 18 years, with 115 affected (64 girls and 51 boys) and 76 unaffected (35 girls and 41 boys) by obesity. Routine clinical assessment and pubertal stage evaluation based upon Tanner's scale were performed. In addition, to evaluate the impact of puberty, children with pre-adolescence and advanced puberty were divided into separate subgroups. Then, 24 h urine steroid excretion profiles were analyzed by gas chromatography/mass spectrometry. Significant differences in the excretion of steroid metabolites were found between normal weight children and children with obesity, especially in the prepubertal cohort. In this group, we observed enhanced activity in all the pathways of adrenal steroidogenesis. Raised excretion of mineralocorticoid derivatives such as tetrahydro-11-deoxycorticosterone, tetrahydrocorticosterone, and 5α-tetrahydrocorticosterone supported increased activity of this track. No significant differences were detected in the excreted free forms of cortisol and cortisone, while the excretion of their characteristic tetrahydro-derivatives was different. In pre-adolescent children with obesity, α-cortol and especially α-cortolone appeared to be excreted more abundantly than β-cortol or β-cortolone. Furthermore, in children with obesity, we observed elevated androgen excretion with an enhanced backdoor pathway. As puberty progressed, remarkable reduction in the differences between adolescents with and without obesity was demonstrated.
儿童肥胖与多种类固醇变化有关,这些变化是由超重引起的。本研究旨在评估肥胖儿童与体重正常儿童的类固醇代谢情况,尤其是与性别和青春期进展的关系。我们分析了 191 名年龄在 5 至 18 岁之间的儿童的临床数据,其中 115 名受肥胖影响(64 名女孩和 51 名男孩),76 名不受影响(35 名女孩和 41 名男孩)。进行了常规临床评估和基于 Tanner 量表的青春期阶段评估。此外,为了评估青春期的影响,将青春期前和青春期后期的儿童分为单独的亚组。然后,通过气相色谱/质谱法分析 24 小时尿液类固醇排泄谱。在体重正常的儿童和肥胖的儿童之间,发现类固醇代谢物的排泄存在显著差异,尤其是在青春期前的儿童中。在这一组中,我们观察到所有肾上腺类固醇生成途径的活性增强。四氢-11-脱氧皮质酮、四氢皮质酮和 5α-四氢皮质酮等盐皮质激素衍生物的排泄增加支持了这一途径的活性增强。未检测到游离形式的皮质醇和可的松的排泄有显著差异,而它们的特征四氢衍生物的排泄则不同。在肥胖的青春期前儿童中,α-考多醇,特别是 α-考多龙,似乎比β-考多醇或β-考多龙排泄得更丰富。此外,在肥胖儿童中,我们观察到雄激素排泄增加,后门途径增强。随着青春期的进展,肥胖青少年和非肥胖青少年之间的差异显著减少。