Department of Pediatric Endocrinology, University Hospital, 49000 Angers, France.
Reference Center for Rare Pituitary Diseases, University Hospital, 49000 Angers, France.
J Clin Endocrinol Metab. 2024 May 17;109(6):1443-1453. doi: 10.1210/clinem/dgad760.
The increase in bone mineral content (BMC) and density (BMD) measured by dual-energy x-ray absorptiometry (DXA) in obese children may not sustain the mechanical load associated with weight, and the factors influencing bone mineralization are not well known.
We described bone mineralization in boys with overweight/obesity and leanness in relation to body composition.
Cross-sectional study in the Pediatric Endocrinology Unit of Angers University Hospital with 249 overweight/obese boys aged 8-18 who underwent DXA and insulin, testosterone, and IGF-1 measurements. Bone mineralization was compared with data from 301 lean boys of similar age and height from NHANES 2011-2015, using the same DXA model. Path analyses were performed to evaluate factors associated with total body less head (TBLH) BMC.
The mean age- and height-adjusted difference in TBLH BMC between obese and lean boys was 241 ± 20 g/cm2. Each 1 kg/m2 increase in BMI was associated with +39 ± 6 g of TBLH BMC in lean subjects vs + 25 ± 3 g in obese subjects (P < .05). Each 1 kg/m2 increase in lean BMI (LBMI) was associated with +78 ± 5 g of TBLH BMC in lean and obese boys, and each 1 kg/m2 increase in fat mass index (FMI) was associated with a decrease of 9 ± 3 g of TBLH BMC. The TBLH BMC was directly positively influenced by LBMI and indirectly and positively influenced by IGF-1, testosterone, and insulin (mediated through height and LBMI). FMI indirectly influenced TBLH BMC, both positively through LBMI and negatively through its negative impact on IGF-1 and testosterone.
The increase in bone mineralization in obese children does not adapt to the increase in body mass.
通过双能 X 射线吸收法(DXA)测量的肥胖儿童的骨矿物质含量(BMC)和密度(BMD)增加可能无法承受与体重相关的机械负荷,并且影响骨矿化的因素尚不清楚。
我们描述了超重/肥胖和消瘦男孩的骨矿化与身体成分的关系。
安格尔大学医院儿科内分泌科进行的横断面研究,纳入 249 名 8-18 岁的超重/肥胖男孩,他们接受了 DXA 和胰岛素、睾酮和 IGF-1 测量。使用相同的 DXA 模型,将骨矿化与来自 NHANES 2011-2015 年的 301 名年龄和身高相似的瘦男孩的数据进行比较。进行路径分析以评估与全身非头(TBLH)BMC 相关的因素。
肥胖男孩和瘦男孩 TBLH BMC 的年龄和身高调整后平均差异为 241 ± 20 g/cm2。在瘦受试者中,每增加 1 kg/m2 的 BMI 与 TBLH BMC 增加 +39 ± 6 g,而在肥胖受试者中增加 +25 ± 3 g(P <.05)。每增加 1 kg/m2 的瘦体重指数(LBMI)与瘦和肥胖男孩的 TBLH BMC 增加 +78 ± 5 g,每增加 1 kg/m2 的脂肪质量指数(FMI)与 TBLH BMC 减少 9 ± 3 g 相关。TBLH BMC 直接受到 LBMI 的正向影响,间接通过 IGF-1、睾酮和胰岛素正向影响(通过身高和 LBMI 介导)。FMI 间接影响 TBLH BMC,通过 LBMI 产生正向影响,通过对 IGF-1 和睾酮的负面影响产生负向影响。
肥胖儿童的骨矿化增加无法适应体重的增加。