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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Deficient bone formation in idiopathic juvenile osteoporosis: a histomorphometric study of cancellous iliac bone.
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Deficient bone formation in idiopathic juvenile osteoporosis: a histomorphometric study of cancellous iliac bone.

机译:特发性青少年骨质疏松症的骨形成不足:松质骨的组织形态计量学研究。

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摘要

Idiopathic juvenile osteoporosis (IJO), a rare cause of osteoporosis in children, is characterized by the occurrence of vertebral and metaphyseal fractures. Little is known about the histopathogenesis of IJO. We analyzed by quantitative histomorphometry iliac crest biopsies from 9 IJO patients (age, 10.0-12.3 years; 7 girls) after tetracycline labeling. Results were compared with identically processed samples from 12 age-matched children without metabolic bone disease and 11 patients with osteogenesis imperfecta type I. Compared with healthy controls, cancellous bone volume (BV) was markedly decreased in IJO patients (mean [SD]: 10.0% [3.1%] vs. 24.4% [3.8%]), because of a 34% reduction in trabecular thickness (Tb.Th) and a 37% lower trabecular number (Tb.N; p < 0.0001 each; unpaired t-test). Bone formation rate (BFR) per bone surface was decreased to 38% of the level in controls (p = 0.0006). This was partly caused by decreased recruitment of remodeling units, as shown by a trend toward lower activation frequency (54% of the control value; p = 0.08). Importantly, osteoblast team performance also was impaired, as evidenced by a decreased wall thickness (W.Th; 70% of the control value; p < 0.0001). Reconstruction of the formative sites revealed that osteoblast team performance was abnormally low even before mineralization started at a given site. No evidence was found for increased bone resorption. Compared with children with osteogenesis imperfecta (OI), IJO patients had a similarly decreased cancellous BV but a much lower bone turnover. These results suggest a pathogenetic model for IJO, in which impaired osteoblast team performance decreases the ability of cancellous bone to adapt to the increasing mechanical needs during growth. This will finally result in load failure at sites where cancellous bone is essential for stability.
机译:特发性青少年骨质疏松症(IJO)是儿童骨质疏松症的罕见病因,其特征是发生椎骨和干phy端骨折。关于IJO的组织病理学知之甚少。在四环素标记后,我们通过定量组织形态计量学对9例IJO患者(年龄为10.0-12.3岁; 7例女孩)的c活检进行了分析。将结果与来自12例年龄相匹配的无代谢性骨病的儿童和11例I型成骨不全患者的相同处理的样品进行比较。与健康对照组相比,IJO患者的松质骨体积(BV)明显减少(平均值[SD]:10.0 %[3.1%]与24.4%[3.8%]),因为小梁厚度(Tb.Th)降低了34%,小梁骨数目降低了37%(Tb.N;每个p <0.0001;未配对t检验)。每个骨骼表面的骨形成率(BFR)降至对照组水平的38%(p = 0.0006)。这部分是由于重塑单元募集减少所致,如激活频率降低的趋势(控制值的54%; p = 0.08)所示。重要的是,成骨细胞组的性能也受到损害,如壁厚减小所证明(W.Th;对照值的70%; p <0.0001)。重建形成部位表明,即使在给定部位开始矿化之前,成骨细胞团队的表现也异常低下。没有发现增加骨吸收的证据。与成骨不全症(OI)患儿相比,IJO患者的松质BV降低程度相似,但骨转换率低得多。这些结果提示了IJO的致病模型,其中成骨细胞团队性能受损,降低了松质骨适应生长过程中不断增长的机械需求的能力。这最终将导致松质骨对于稳定性至关重要的部位的负载失效。

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