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Transient micro-elastography: A novel non-invasive approach to measure liver stiffness in mice

机译:瞬态微弹性成像:一种新颖的非侵入性方法来测量小鼠的肝脏僵硬

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摘要

AIM: To develop and validate a transient micro-elastography device to measure liver stiffness (LS) in mice.METHODS: A novel transient micro-elastography (TME) device, dedicated to LS measurements in mice with a range of measurement from 1-170 kPa, was developed using an optimized vibration frequency of 300 Hz and a 2 mm piston. The novel probe was validated in a classical fibrosis model (CCl4) and in a transgenic murine model of systemic amyloidosis.RESULTS: TME could be successfully performed in control mice below the xiphoid cartilage, with a mean LS of 4.4 ± 1.3 kPa, a mean success rate of 88%, and an excellent intra-observer agreement (0.98). Treatment with CCl4 over seven weeks drastically increased LS as compared to controls (18.2 ± 3.7 kPa vs 3.6 ± 1.2 kPa). Moreover, fibrosis stage was highly correlated with LS (Spearman coefficient = 0.88, P < 0.01). In the amyloidosis model, much higher LS values were obtained, reaching maximum values of > 150 kPa. LS significantly correlated with the amyloidosis index (0.93, P < 0.0001) and the plasma concentration of mutant hapoA-II (0.62, P < 0.005).CONCLUSION: Here, we have established the first non-invasive approach to measure LS in mice, and have successfully validated it in two murine models of high LS.
机译:目的:开发和验证一种用于测量小鼠肝硬度(LS)的瞬态微弹性成像设备方法:一种新型的瞬态微弹性成像(TME)设备,专用于小鼠的LS测量,测量范围从1-170 kPa是使用300 Hz的优化振动频率和2 mm活塞开发的。该新型探针已在经典纤维化模型(CCl4)和系统性淀粉样变性的转基因鼠模型中得到验证。结果:TME可以成功地在剑突软骨以下的对照组小鼠中进行,平均LS为4.4±1.3 kPa,平均成功率为88%,并且观察员内部协议非常出色(0.98)。与对照组相比,用CCl4处理超过7周的LS大大增加(18.2±3.7 kPa对3.6±1.2 kPa)。此外,纤维化分期与LS高度相关(Spearman系数= 0.88,P <0.01)。在淀粉样变性模型中,获得了更高的LS值,达到了> 150 kPa的最大值。 LS与淀粉样变性指数(0.93,P <0.0001)和突变体hapoA-II的血浆浓度(0.62,P <0.005)显着相关。并已在两个高LS小鼠模型中成功验证了它。

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