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Severe injury-induced osteoporosis and skeletal muscle mineralization: Are these related complications?

机译:严重损伤诱导的骨质疏松症和骨骼肌矿化:这些相关并发症是什么?

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摘要

Severely injured patients are beleaguered by complications during convalescence, such as dysregulated biomineralization. Paradoxically, severely injured patients experience the loss of bone (osteoporosis), resulting in diminished skeletal integrity and increased risk of fragility fractures; yet they also accrue mineralization in soft tissues, resulting in complications such as heterotopic ossification (HO). The pathophysiology leading to dysregulated biomineralization in severely injured patients is not well defined. It has been postulated that these pathologies are linked, such that mineralization is “transferred” from the bone to soft tissue compartments. The goal of this study was to determine if severe injury-induced osteoporosis and soft tissue calcification are temporally coincident following injury. Using a murine model of combined burn and skeletal muscle injury to model severe injury, it was determined that mice developed significant progressive bone loss, detectable as early as 3 days post injury, and marked soft tissue mineralization by 7 days after injury. The observed temporal concordance between the development of severe injury-induced osteoporosis and soft tissue mineralization indicates the plausibility that these complications share a common pathophysiology, though further experiments are required.
机译:严重受伤的患者在康复期间的并发症是令人生畏的,例如具有疑难解的生物矿化。矛盾的伤害患者体验骨骼(骨质疏松症)的丧失,导致骨骼完整性减少和脆性骨折的风险增加;然而,它们也在软组织中累积矿化,导致过型骨化(HO)等并发症。在严重受伤的患者中导致失调生物蛋白化的病理生理学并不明确。已经提出了这些病理链接,使得矿化从骨骼“转移”到软组织隔室。本研究的目标是确定严重损伤诱导的骨质疏松症和软组织钙化是否在损伤后暂时重合。利用组合烧伤和骨骼肌损伤的鼠模型模拟严重损伤,确定小鼠显着的渐进性骨质损失,损伤后3天可检测到,损伤后7天明显良好的组织矿化。观察到的严重损伤骨质疏松症和软组织矿化的发育之间的时间相应表明,这些并发症共享了常见病理生理学的合理性,但是需要进一步的实验。

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