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接受静脉注射帕米膦酸的小儿成骨不全症患者中的大型破骨细胞。

Large osteoclasts in pediatric osteogenesis imperfecta patients receiving intravenous pamidronate.

作者信息

Cheung Moira S, Glorieux Francis H, Rauch Frank

机构信息

Genetics Unit, Shriners Hospital for Children and McGill University, Montreal, Quebec, Canada.

出版信息

J Bone Miner Res. 2009 Apr;24(4):669-74. doi: 10.1359/jbmr.081225.

Abstract

Intravenous pamidronate is widely used to treat children with moderate to severe osteogenesis imperfecta (OI). Changes in the appearance of osteoclasts have previously been noted in children receiving pamidronate and have been interpreted as signs of toxicity. In this study, we analyzed osteoclast parameters in paired iliac bone specimens before and after 2-4 yr of cyclical intravenous pamidronate therapy in 44 pediatric OI patients (age range: 1.4-17.5 yr; 21 girls). During pamidronate treatment, average osteoclast diameter and the mean number of nuclei present per osteoclast increased by 18% (p = 0.02) and 43% (p < 0.001), respectively. The number of samples containing large osteoclasts (LOcs, diameter > 50 mum) increased from 6 (14%) before treatment to 23 (52%) after pamidronate therapy (p < 0.001 by chi(2) test). Post-treatment samples containing LOcs had a greater core width (p = 0.04) and a higher cancellous bone volume per tissue volume (p < 0.001), because cancellous bone volume had increased more during pamidronate treatment (p < 0.001). Osteoclast number and surface were higher in samples with LOcs, but there was no difference in cancellous bone formation parameters. The presence of LOcs was independent of OI type, type of collagen type I mutation, lumbar spine BMD, and other clinical or biochemical measures. In conclusion, this study did not show any indication that LOcs during pamidronate treatment are indicative of toxicity. It seems more likely that the observed abnormalities in osteoclast morphology are part of the mechanism of action of this drug.

摘要

静脉注射帕米膦酸盐被广泛用于治疗中重度成骨不全症(OI)患儿。此前在接受帕米膦酸盐治疗的患儿中已注意到破骨细胞外观的变化,并被解释为毒性迹象。在本研究中,我们分析了44例小儿OI患者(年龄范围:1.4 - 17.5岁;21名女孩)在接受2 - 4年周期性静脉注射帕米膦酸盐治疗前后成对髂骨标本中的破骨细胞参数。在帕米膦酸盐治疗期间,破骨细胞平均直径和每个破骨细胞的平均核数分别增加了18%(p = 0.02)和43%(p < 0.001)。含有大破骨细胞(LOcs,直径> 50μm)的样本数量从治疗前的6个(14%)增加到帕米膦酸盐治疗后的23个(52%)(经卡方检验,p < 0.001)。含有LOcs的治疗后样本具有更大的核心宽度(p = 0.04)和更高的每组织体积松质骨体积(p < 0.001),因为在帕米膦酸盐治疗期间松质骨体积增加得更多(p < 0.001)。含有LOcs的样本中破骨细胞数量和表面积更高,但松质骨形成参数没有差异。LOcs的存在与OI类型、I型胶原突变类型、腰椎骨密度以及其他临床或生化指标无关。总之,本研究未显示任何迹象表明帕米膦酸盐治疗期间的LOcs表明存在毒性。观察到的破骨细胞形态异常似乎更有可能是该药物作用机制的一部分。

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