Histomorphometric analysis of glucocorticoid-induced osteoporosis

被引:47
作者
Carbonare, LD [1 ]
Bertoldo, F
Valenti, MT
Zenari, S
Zanatta, M
Sella, S
Giannini, S
Lo Cascio, V
机构
[1] Univ Verona, Dept Biomed & Surg Sci, I-37100 Verona, Italy
[2] Univ Padua, Med Clin 1, Dept Med & Surg Sci, Padua, Italy
关键词
histomorphometry; bisphosphonates; glucocorticoids; microarchitecture; osteoporosis;
D O I
10.1016/j.micron.2005.07.009
中图分类号
TH742 [显微镜];
学科分类号
摘要
Bone histomorphometry or quantitative histology consists of counting or measuring tissue components: cells, extracellular constituents and microarchitecture. Bone histomorphometry is the only method that allows the measurement of mineralization rate and the study of bone formation at three levels: cell, remodeling unit and tissue levels. It is a useful tool to explain the pathogenesis and cellular mechanisms of different metabolic bone diseases such as glucocorticoid-induced osteoporosis (GIO). Glucocorticoids (GC) affect calcium and bone metabolism at every level, but the main effect is the osteoblastic dysfunction. Concerning the bone formation, some histomorphometric studies have shown a depressed osteoblastic activity at a cell, bone remodeling unit, and tissue levels. In addition, there is evidence of a shortening of the period in which the osteoblasts work actively forming the bone matrix. This latter effect seems to occur after high cumulative doses of GC. With regard to the resorption, the results are still debated, but histomorphometric parameters seem to be increased in the majority of studies, at least in the first period of the GC treatment. From a structural point of view, GC seem to induce a thinning of the trabeculae without their perforation, which occurs only after high cumulative doses. Antiresorptive treatments, such as bisphosphonates, are able to counteract the negative effects of GC on bone. In particular, along with their active working period, they prolong the lifespan of osteoblasts and osteocytes. In addition, the antiresorptive treatments seem to extend the time for secondary mineralization through a reduction of the Activation Frequency. The latter is an intriguing mechanism of bisphosphonates in GIO that needs further ad hoc investigations. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:645 / 652
页数:8
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