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The effect of thiazolidinediones on BMD and osteoporosis.

机译:噻唑烷二酮对骨密度和骨质疏松的影响。

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摘要

Thiazolidinediones, also known as glitazones, are insulin-sensitizing medications that account for approximately 21% of oral antihyperglycemic drugs used in the US. Although the main therapeutic effects occur in adipose tissue, muscles and the liver, studies suggest effects in bone as well. Currently, two thiazolidinediones are marketed in the US-rosiglitazone and pioglitazone-and several others are under investigation. This Review examines the evidence regarding the effects of thiazolidinediones on skeletal health. These drugs appear to trigger preferential differentiation of mesenchymal stem cells into adipocytes rather than osteoblasts, leading to decreased bone formation and increased adipogenesis. Although only a few small, randomized studies have examined the effects of thiazolidinediones on bone in humans, the available data suggest that these agents contribute to bone loss in postmenopausal women; the relationship is less clear in men. On the basis of this limited evidence, the absolute increase in fracture risk associated with thiazolidinediones seems to be small. Pending data from future randomized, controlled trials of the association between thiazolidinediones and low bone mass, prescribers should consider use of these drugs as a risk factor for the development of osteoporosis in postmenopausal women.
机译:噻唑烷二酮,也称为格列酮类,是胰岛素敏感性药物,约占美国口服降血糖药的21%。尽管主要的治疗作用发生在脂肪组织,肌肉和肝脏中,但研究表明对骨骼也有作用。目前,在美国销售两种噻唑烷二酮类药物:罗格列酮和吡格列酮,其他几种正在研究中。这篇评论研究了噻唑烷二酮对骨骼健康的影响的证据。这些药物似乎触发了间充质干细胞优先分化为脂肪细胞而不是成骨细胞,从而导致骨形成减少和脂肪生成增加。尽管只有少数小型随机研究检查了噻唑烷二酮对人体骨骼的影响,但现有数据表明这些药物可导致绝经后妇女的骨质流失。男人之间的关系不太清楚。根据这一有限的证据,与噻唑烷二酮有关的骨折风险的绝对增加似乎很小。在获得来自未来噻唑烷二酮类药物与低骨量相关性的随机对照试验的数据之前,处方者应考虑将这些药物用作绝经后妇女骨质疏松症发展的危险因素。

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