Jang Yohan, Lopas Luke A, Foley David P, McKinley Todd O, Mullis Brian H, Collier Christopher D, Liu Ziyue, Kacena Melissa A, Natoli Roman M
Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Indiana Center for Musculoskeletal Health (ICMH), Indiana University School of Medicine, Indianapolis, Indiana.
J Bone Joint Surg Am. 2025 Jul 10;107(16):1841-1847. doi: 10.2106/JBJS.24.01304.
Researchers employ murine fracture models to study bone healing, but the temporal relationship between mouse and human fracture healing is poorly understood. The hypothesis of this study was that it was possible to quantify specific post-fracture time frames corresponding to the stages of endochondral ossification in both mice and humans.
Radiographs of mice and human femoral fractures treated with intramedullary stabilization were reviewed. The study included 330 human femoral fractures (OTA/AO 32A, B, or C injuries) that ultimately healed without complications in patients aged 18 to 55 years and 309 surgically created midshaft femoral fractures in 3-month-old C57BL6/J mice. Multiple orthopaedic surgeons assessed the radiographs using the Modified Radiographic Union Score for Tibia (mRUST). A 4-parameter log-logistic curve was fit to describe fracture healing over time, with 3 parameters allowed to vary: Y∞ (mRUST score at time = ∞), k (healing rate in [1/log(time)]), and X0.5 (time to half-healing).
The values (and 95% confidence interval) for the mice were Y∞ = 14.70 (14.54 to 14.87), k = 4.54/log(days) (4.30 to 4.77), and X0.5 = 11.77 days (11.56 to 11.98). For the humans, the values were Y∞ = 16.78 (16.21 to 17.36), k = 1.37/log(days) (1.28 to 1.45), and X0.5 = 91 days (83 to 99). All parameters differed significantly between the mice and humans (p < 0.05).
Using mRUST scoring and mathematical modeling, we were able to quantify and compare the temporal progression of fracture healing in mice and humans.
These data are relevant for designing and/or interpreting fracture healing studies of mice and humans to promote rational translation of fracture research between species.
研究人员采用小鼠骨折模型来研究骨愈合,但小鼠和人类骨折愈合之间的时间关系尚不清楚。本研究的假设是,有可能量化与小鼠和人类软骨内成骨阶段相对应的特定骨折后时间框架。
回顾了接受髓内固定治疗的小鼠和人类股骨骨折的X线片。该研究纳入了330例人类股骨骨折(OTA/AO 32A、B或C型损伤),这些骨折最终在18至55岁的患者中顺利愈合且无并发症,以及309例在3月龄C57BL6/J小鼠中手术制造的股骨干中段骨折。多名骨科医生使用改良的胫骨X线愈合评分(mRUST)对X线片进行评估。采用四参数对数-逻辑曲线来描述骨折愈合随时间的变化,允许三个参数变化:Y∞(时间=∞时的mRUST评分)、k([1/log(时间)]中的愈合率)和X0.5(愈合至一半的时间)。
小鼠的数值(及95%置信区间)为Y∞ = 14.70(14.54至14.87),k = 4.54/log(天)(4.30至4.77),X0.5 = 11.77天(11.56至11.98)。人类的数值为Y∞ = 16.78(16.21至17.36),k = 1.37/log(天)(1.28至1.45),X0.5 = 91天(83至99)。小鼠和人类之间所有参数均有显著差异(p < 0.05)。
使用mRUST评分和数学建模,我们能够量化并比较小鼠和人类骨折愈合的时间进程。
这些数据对于设计和/或解释小鼠和人类的骨折愈合研究具有相关性,以促进不同物种间骨折研究的合理转化。