Keshawarz N M, Recker R R
Bone. 1986;7(2):83-7. doi: 10.1016/8756-3282(86)90678-2.
Thirty-four normal Caucasian women and 69 patients with osteoporosis were given two bone-labeling agents. Transilial biopsies were obtained and embedded undecalcified. Fractional surfaces covered by double label and single label were determined, along with total surface and double label width by fluorescent microscopy. Mean wall thickness was measured on toluidine blue-stained sections. The mathematical model for predicting the amount of single-labeled surface was compared to the actual amount of surface covered by single label. We found an excess of single labels compared to the model in both groups, more so in the normals, and suggest the explanation is that bone-formation pauses at formation sites in both groups but tends not to resume in the patients. This results in a shortened functional life span of the osteoblast and bone loss. Further, the data suggest that for accurate expression of bone formation rates in trabecular bone using a volume referent, one should use the whole bone tissue including bone and marrow and should express the bone-forming surface as the double-labeled surface plus one-half the measured single-labeled surface.
34名正常白种女性和69名骨质疏松症患者接受了两种骨标记剂。获取了经髂骨活检组织并进行不脱钙包埋。通过荧光显微镜确定双标记和单标记覆盖的分数表面,以及总表面和双标记宽度。在甲苯胺蓝染色切片上测量平均壁厚度。将预测单标记表面量的数学模型与单标记实际覆盖的表面量进行比较。我们发现两组中与模型相比单标记都过量,正常组更明显,并认为解释是两组中骨形成在形成部位暂停,但患者组往往不再恢复。这导致成骨细胞功能寿命缩短和骨质流失。此外,数据表明,为了使用体积参照准确表达小梁骨中的骨形成率,应该使用包括骨和骨髓的整个骨组织,并将骨形成表面表示为双标记表面加上测量的单标记表面的一半。