首页> 美国卫生研究院文献>Frontiers in Endocrinology >Evidence for Ongoing Modeling-Based Bone Formation in Human Femoral Head Trabeculae via Forming Minimodeling Structures: A Study in Patients with Fractures and Arthritis
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Evidence for Ongoing Modeling-Based Bone Formation in Human Femoral Head Trabeculae via Forming Minimodeling Structures: A Study in Patients with Fractures and Arthritis

机译:通过形成微型模型结构在人类股骨头小梁中持续进行基于模型的骨形成的证据:骨折和关节炎患者的一项研究

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摘要

Bone modeling is a biological process of bone formation that adapts bone size and shape to mechanical loads, especially during childhood and adolescence. Bone modeling in cortical bone can be easily detected using sequential radiographic images, while its assessment in trabecular bone is challenging. Here, we performed histomorphometric analysis in 21 bone specimens from biopsies collected during hip arthroplasty, and we proposed the criteria for histologically identifying an active modeling-based bone formation, which we call a “forming minimodeling structure” (FMiS). Evidence of FMiSs was found in 9 of 20 specimens (45%). In histomorphometric analysis, bone volume was significant higher in specimens displaying FMiSs compared with the specimens without these structures (BV/TV, 31.7 ± 10.2 vs. 23.1 ± 3.9%; p < 0.05). Osteoid parameters were raised in FMiS-containing bone specimens (OV/BV, 2.1 ± 1.6 vs. 0.6 ± 0.3%; p < 0.001, OS/BS, 23.6 ± 15.5 vs. 7.6 ± 4.2%; p < 0.001, and O.Th, 7.4 µm ± 2.0 vs. 5.2 ± 1.0; p < 0.05). Our results showed that the modeling-based bone formation on trabecular bone surfaces occurs even during adulthood. As FMiSs can represent histological evidence of modeling-based bone formation, understanding of this physiology in relation to bone homeostasis is crucial.
机译:骨骼建模是骨骼形成的生物学过程,可以使骨骼的大小和形状适应机械负荷,尤其是在儿童期和青春期。可以使用连续的放射线图像轻松检测皮质骨的骨模型,而其在小梁骨中的评估却具有挑战性。在这里,我们对从髋关节置换术中收集的活检样本中的21个骨标本进行了组织形态计量学分析,我们提出了组织学上识别基于活动建模的骨形成的标准,我们将其称为“形成微型模型结构”(FMiS)。在20个标本中的9个(45%)中发现了FMiSs的证据。在组织形态计量学分析中,与没有这些结构的标本相比,显示FMiSs的标本中的骨体积显着更高(BV / TV,31.7%±10.2%对23.1%±3.9%; p <0.05)。类骨质参数在含FMiS的骨标本中升高(OV / BV,2.1±±1.6 vs. 0.6±±0.3%; p <0.001,OS / BS,23.6±15.5与7.6±4.2%; p <0.001,O. Th,7.4μm±2.0,相对于5.2±1.0; p <0.05。我们的结果表明,即使在成年期,在小梁骨表面上也会发生基于模型的骨形成。由于FMiS可以代表基于建模的骨形成的组织学证据,因此了解与骨稳态有关的这种生理至关重要。

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