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Imaging-Based Biomarkers: Characterization of Post-Kawasaki Vasculitis in Infants and Hypertension Phenotype in Rat Model

机译:基于成像的生物标记物:川崎后血管炎在婴儿和大鼠高血压表型中的表征。

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Background. Investigating the mechanical properties of the arteries is essential in cardiovascular diseases. Recent imaging modalities allow mapping mechanical properties within the arterial wall.Aims. We report the potential ofimaging-based biomarker(ImBioMark) to investigate the effect of aging on the rat. We also present preliminary data with ImBioMark characterizing vascular sequelae of Kawasaki disease (KD) in young humans.Methods. We investigatedin vivothe effect of aging on male Brown Norway (BN) rats' (n=5) carotid stiffness. In a second experiment, the impact of KD on the ascending aorta (AA) was examined in KD children (n=2) aged 13 ± 1.41 years old compared to KD-free children (n=5) aged 13.13 ± 0.18 years old.Results. The stiffness of BN's carotid artery was three times stiffer in the old rats, with a turning point at 40 weeks old (P=0.001). KD had a very significant impact on the AA stiffness with strain estimates of 2.39 ± 0.51% versus 4.24 ± 0.65% in controls (P<0.001).Conclusion. ImBioMark phenotypes hypertension in rat models noninvasivelyin vivowithout resorting to euthanasia. Quantifying aortic wall remodeling is also feasible in humans. Future investigations target human cardiovascular disease.
机译:背景。在心血管疾病中,研究动脉的机械特性至关重要。最近的成像方式允许在动脉壁内绘制机械特性图。我们报告了基于影像的生物标记物(ImBioMark)的潜力,以研究衰老对大鼠的影响。我们还提供了用ImBioMark表征年轻人川崎病(KD)血管后遗症的初步数据。我们在体内研究了衰老对雄性布朗挪威(BN)大鼠(n = 5)颈动脉僵硬度的影响。在第二个实验中,与年龄在13.13±0.18岁的无KD儿童(n = 5)相比,在13±1.41岁的KD儿童(n = 2)中检查了KD对升主动脉(AA)的影响。结果。在老龄大鼠中,BN的颈动脉僵硬程度是其三倍,转折点为40周大(P = 0.001)。 KD对AA刚度有非常显着的影响,应变估计为2.39±0.51%,而对照组为4.24±0.65%(P <0.001)。大鼠体内的ImBioMark表型高血压无创性地采用了无创性安乐死。在人类中量化主动脉壁重塑也是可行的。未来的研究针对人类心血管疾病。

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