在胶原酶诱导的小鼠模型中使用显微计算机断层扫描揭示骨关节炎进展的早期软骨下骨结构变化

H. Liu, Z. Li, C.E. Davey, K.S. Stok
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引用次数: 0

摘要

微计算机断层扫描(microCT)的部署使定量形态分析(QMA)能够以极好的空间分辨率量化小鼠膝关节OA引起的形态和结构变化。先前的研究每隔两周量化软骨下胫骨的微结构变化,报告早在小鼠模型疾病诱导后两周骨丢失和小梁变薄。然而,有证据表明,在小鼠OA模型中,软骨下骨转换可能早于疾病诱导后两周发生。目的利用微ct和QMA技术揭示高时间分辨率小鼠骨关节炎进展的早期骨微结构变化。方法招募9周龄雄性C57BL/10小鼠75只,随机分为基线组(n = 4)、对照组(n = 24)和OA组(n = 47)3个横断面队列。选取10周龄OA组小鼠47只,经髌骨韧带向右侧关节(OA组)关节内注射溶解于6µl生理盐水中过滤后的胶原酶10单位。左对侧关节内注射等量生理盐水(CTLR组)。在扫描前,小鼠在0、1、2、3、4、5、6、7和8周时被安乐死。扫描使用microCT (vivaCT80, SCANCO Medical AG, br ttisellen, Switzerland)进行,源电压为70 kVp,积分时间为350 ms,电流为114µa,标称分辨率为10.4µm, 500个投影,每次扫描大约需要20分钟。QMA用于量化与骨关节炎进展相关的软骨下骨微结构的变化。为了检测各时间点处理间的差异,采用线性混合效应模型。个体小鼠被认为是随机效应,时间点(胶原酶注射后1- 8周)和治疗(CT、CTLR和OA)被认为是固定效应。Figure 1a为CT组和OA组具有代表性的微CT分割图像。OA组在多个时间点观察到典型的骨关节炎特征,早在疾病诱导后一周就可以检测到变化,如图1 b所示。其中,对比CT组和CTLR组的关节,骨小梁厚度较小,Tb。随着骨小梁间距的增加,在OA股骨的外侧和内侧均观察到Th。结论本研究首次证实,早在疾病诱导后1周就可以检测到明显的骨变化。这些发现强调了早期量化的必要性,以捕获早期OA中快速变化的骨微观结构改变,从而有可能实现早期诊断、干预和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
REVEALING EARLY SUBCHONDRAL BONE STRUCTURAL CHANGES IN OSTEOARTHRITIS PROGRESSION IN A COLLAGENASE-INDUCED MOUSE MODEL USING MICRO COMPUTED TOMOGRAPHY

INTRODUCTION

The deployment of micro-computed tomography (microCT) enables quantitative morphometric analysis (QMA) to quantify morphological and structural changes caused by OA in mouse knee joint with excellent spatial resolution. Previous studies quantifying microstructural changes to subchondral tibiae in fortnightly intervals, report bone loss and trabecular thinning as early as two weeks post disease induction in mouse models. However, evidence suggests that the subchondral bone turnover may occur earlier than two weeks post disease induction in a mouse OA model.

OBJECTIVE

To reveal early bone microstructural changes associated with OA progression in a mouse model with a high temporal resolution using microCT and QMA.

METHODS

Seventy-five male C57BL/10 mice aged nine weeks were recruited and randomly assigned to three cross-sectional cohorts, i.e., baseline (n = 4), control (n = 24) and OA (n = 47) cohorts. Forty-seven ten-week-old mice assigned to OA cohort received intra-articular injection of 10 unit of filtered collagenase dissolved in 6 µl physiological saline to the right joints (OA group) through the patellar ligament. A similar volume of saline was intraarticularly injected to the left contralateral joints (CTLR group). Prior to scanning, mice were euthanized at 0-, 1-, 2-, 3-, 4-, 5-, 6-, 7-, and 8-weeks post ten-week-old. Scans were performed using microCT (vivaCT80, SCANCO Medical AG, Brüttisellen, Switzerland) with a source voltage of 70 kVp, an integration time of 350 ms, a current of 114 µA, a nominal resolution of 10.4 µm, and 500 projections with each scan taking around 20 minutes. QMA was performed to quantify changes to subchondral bone microstructure associated with OA progression. To detect differences between treatments at each time point, a linear mixed-effect model was used. Individual mice were considered as random effects, time points (1- to 8- weeks post collagenase injection) and treatment (CT, CTLR, and OA) were considered as fixed effects.

RESULTS

Representative segmented microCT images from CT and OA group can be found in Figure 1 A. Typical osteoarthritic characteristics were observed in OA group at multiple time points, with changes detectable as early as one week post disease induction, shown in Figure 1 B. Specifically, comparing joints from CT and CTLR groups, smaller trabecular thickness, Tb.Th, were observed at both lateral and medial sides in OA femora, in accordance with the increasing trabecular spacing, Tb.Sp, and decreasing trabecular number, Tb.N.

CONCLUSION

This study, for the first time, demonstrated that prominent bone changes could be detected as early as one week after disease induction. These findings underscore the necessity of early quantification to capture rapidly changing bone microstructure alterations in early stage OA, potentially enabling earlier diagnosis, intervention, and treatment.
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Osteoarthritis imaging
Osteoarthritis imaging Radiology and Imaging
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