Byers R J, Denton J, Hoyland J A, Freemont A J
University of Manchester Bone Disease Research Centre, Department of Pathological Sciences, University of Manchester, UK.
J Clin Pathol. 1997 Sep;50(9):760-4. doi: 10.1136/jcp.50.9.760.
To analyse osteoblast function in 153 cases of established osteoporosis as previous work has indicated that osteoporosis is a heterogeneous condition characterised by different patterns of osteoclast and osteoblast dysfunction.
Histomorphometric data from 153 cases with established osteoporosis was used to analyse osteoblast function, using the following parameters: osteoblast number was assessed using the ratio of osteoblast surface to bone surface (ObS:BS); the percentage of active osteoblasts was assessed by using mineralising surface as a proportion of osteoid surface (sLS + dLS/OS); and the efficiency of active osteoblasts was assessed using the ratio of double to total labelled surface (dLS:tLS). The values of each parameter were standardised using age and sex matched control data and a three dimensional matrix was used to identify groups of patients with similar patterns of altered function.
The largest group (60 cases) showed a reduction in all three parameters, while a small group (9 cases) had normal osteoblast function. However, one group showed reduction in osteoblast number only (23 cases), while another group showed a normal number of osteoblasts but both reduced percentage and efficiency of activity (14 cases). The results also suggest that efficiency of activity falls first and that this eventually leads to exit from the active pool.
These results demonstrate the presence of heterogeneity of osteoblast dysfunction in osteoporosis, indicating that the disease is caused by interference at a variety of target sites along the pathway of osteoblast proliferation, differentiation, and activation. Greater understanding of this pathway and of the variety of alterations in the pathway that can occur in osteoporosis may allow more focused therapy for different patient groups identified on the basis of histomorphometric analysis.
鉴于先前的研究表明骨质疏松症是一种异质性疾病,其特征为破骨细胞和成骨细胞功能的不同模式,本研究旨在分析153例确诊骨质疏松症患者的成骨细胞功能。
利用153例确诊骨质疏松症患者的组织形态计量学数据来分析成骨细胞功能,采用以下参数:成骨细胞数量通过成骨细胞表面与骨表面的比值(ObS:BS)进行评估;活跃成骨细胞的百分比通过矿化表面占类骨质表面的比例(sLS + dLS/OS)进行评估;活跃成骨细胞的效率通过双倍标记表面与总标记表面的比值(dLS:tLS)进行评估。每个参数的值均使用年龄和性别匹配的对照数据进行标准化处理,并使用三维矩阵来识别功能改变模式相似的患者组。
最大的一组(60例)在所有三个参数上均表现出降低,而一小部分(9例)成骨细胞功能正常。然而,一组仅显示成骨细胞数量减少(23例),而另一组显示成骨细胞数量正常,但活性百分比和效率均降低(14例)。结果还表明,活性效率首先下降,最终导致从活跃池中退出。
这些结果证明骨质疏松症中存在成骨细胞功能障碍的异质性,表明该疾病是由成骨细胞增殖、分化和激活途径上的多个靶点受到干扰所致。对该途径以及骨质疏松症中该途径可能发生的各种改变有更深入的了解,可能有助于为基于组织形态计量学分析确定的不同患者群体提供更有针对性的治疗。