Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, United States; Pediatric Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, United States.
Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, United States.
Bone. 2018 Jan;106:61-68. doi: 10.1016/j.bone.2017.07.009. Epub 2017 Jul 8.
Altered bone microarchitecture and higher marrow adipose tissue (MAT) may reduce bone strength. High resolution pQCT (HRpQCT) allows assessment of volumetric BMD (vBMD), and size and microarchitecture parameters of bone, while 1H-magnetic resonance spectroscopy (1H-MRS) allows MAT evaluation. We have reported impaired microarchitecture at the non-weight bearing radius in adolescents with anorexia nervosa (AN) and that these changes may precede aBMD deficits. Data are lacking regarding effects of AN on microarchitecture and strength at the weight-bearing tibia in adolescents and young adults, and the impact of changes in microarchitecture and MAT on strength estimates.
To compare strength estimates at the distal tibia in adolescents/young adults with AN and controls in relation to vBMD, bone size and microarchitecture, and spine MAT.
This was a cross-sectional study of 47 adolescents/young adults with AN and 55 controls 14-24years old that assessed aBMD and body composition using DXA, and distal tibia vBMD, size, microarchitecture and strength estimates using HRpQCT, extended cortical analysis, individual trabecular segmentation, and finite element analysis. Lumbar spine MAT (1H-MRS) was assessed in a subset of 19 AN and 22 controls.
Areal BMD Z-scores were lower in AN than controls. At the tibia, AN had greater cortical porosity, lower total and cortical vBMD, cortical area and thickness, trabecular number, and strength estimates than controls. Within AN, strength estimates were positively associated with lean mass, aBMD, vBMD, bone size and microarchitectural parameters. MAT was higher in AN, and associated inversely with strength estimates.
Adolescents/young adults with AN have impaired microarchitecture at the weight-bearing tibia and higher spine MAT, associated with reduced bone strength.
骨微观结构的改变和更高的骨髓脂肪组织(MAT)可能会降低骨强度。高分辨率 pQCT(HRpQCT)允许评估体积骨密度(vBMD)以及骨的大小和微观结构参数,而 1H 磁共振波谱(1H-MRS)允许评估 MAT。我们已经报道了厌食症(AN)青少年非承重半径处的微观结构受损,并且这些变化可能先于 aBMD 不足。关于 AN 对青少年和年轻成年人承重胫骨的微观结构和强度的影响,以及微观结构和 MAT 变化对强度估计的影响的数据尚缺乏。
比较 AN 青少年/年轻成年人和对照组在远端胫骨的强度估计值与 vBMD、骨大小和微观结构以及脊柱 MAT 的关系。
这是一项横断面研究,纳入了 47 名 AN 青少年/年轻成年人和 55 名年龄在 14-24 岁的对照组,使用 DXA 评估 aBMD 和身体成分,使用 HRpQCT、扩展皮质分析、个体小梁分割和有限元分析评估远端胫骨 vBMD、大小、微观结构和强度估计值。在一组 19 名 AN 和 22 名对照组中评估了腰椎 MAT(1H-MRS)。
与对照组相比,AN 的面积 BMD Z 评分较低。在胫骨处,与对照组相比,AN 的皮质孔隙率较高,总和皮质 vBMD、皮质面积和厚度、小梁数量和强度估计值较低。在 AN 中,强度估计值与瘦体重、aBMD、vBMD、骨大小和微观结构参数呈正相关。MAT 在 AN 中较高,与强度估计值呈负相关。
承重胫骨的微观结构受损和脊柱 MAT 较高,与骨强度降低有关,这是青少年/年轻成年人 AN 的特征。