Moore-Lotridge Stephanie N, Ihejirika Rivka, Gibson Breanne H Y, Posey Samuel L, Mignemi Nicholas A, Cole Heather A, Hawley Gregory D, Uppuganti Sasidhar, Nyman Jeffry S, Schoenecker Jonathan G
Department of Orthopaedics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Center of Bone Biology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Bone Rep. 2020 Dec 26;14:100743. doi: 10.1016/j.bonr.2020.100743. eCollection 2021 Jun.
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.
重伤患者在康复过程中受到并发症的困扰,如生物矿化失调。矛盾的是,重伤患者会出现骨质流失(骨质疏松症),导致骨骼完整性下降和脆性骨折风险增加;然而,他们的软组织中也会出现矿化,导致诸如异位骨化(HO)等并发症。导致重伤患者生物矿化失调的病理生理学尚未明确界定。据推测,这些病理情况是相互关联的,以至于矿化从骨骼“转移”到了软组织中。本研究的目的是确定重伤诱导的骨质疏松症和软组织钙化在受伤后是否在时间上同步发生。使用烧伤和骨骼肌损伤相结合的小鼠模型来模拟重伤情况,结果发现小鼠出现了明显的进行性骨质流失,早在受伤后3天就可检测到,并且在受伤后7天出现明显的软组织矿化。重伤诱导的骨质疏松症和软组织矿化在时间上的一致性表明,这些并发症可能具有共同的病理生理学,但仍需要进一步的实验来验证。