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首页> 外文期刊>Journal of magnetic resonance imaging: JMRI >Early registration of diffusion tensor images for group tractography of dystonia patients
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Early registration of diffusion tensor images for group tractography of dystonia patients

机译:弥散张量图像的早期配准,用于肌张力障碍患者的团体体层摄影

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Purpose: To make a group comparison of diffusion tensor imaging (DTI) results of dystonia patients and controls to reveal occult pathology. We propose using an early registration method that produces sharper group images and enables us to do group tractography. Materials and Methods: Twelve dystonia patients manifesting the disease, seven nonmanifesting dystonia mutation carriers (DYT1 and DYT6 gene mutations), and eight age-matched normal control subjects were imaged for a previous study. Early and late registration methods for DTI were compared. An early registration technique for a super set was proposed, in which the diffusion-weighted images were registered to a template, gradient vectors were reoriented for each subject, and they were combined into a super set before tensor calculation. The super set included images from all subjects and was useful for group comparisons. We used results obtained from the early registration of a super set for group analysis of tracts using the deterministic fiber-tracking technique. Results: In dystonia mutation carriers, we detected fewer fibers in the cerebello-thalamo-cortical pathways. This result agrees well with the findings of a previous study that utilized a probabilistic tractography method and demonstrated that gene carriers have less fiber tracts in the disease-involved pathway. Conclusion: This analysis visualized group level white matter fractional anisotropy and tract differences between dystonia patients and controls, and can be useful in understanding the pathophysiology of other nonfocal white matter diseases. J. Magn. Reson. Imaging 2013;37:67-75.
机译:目的:对肌张力障碍患者和对照组的弥散张量成像(DTI)结果进行分组比较,以揭示隐匿性病理。我们建议使用早期配准方法,以产生更清晰的团体图像,并使我们能够进行团体体检。材料和方法:对12例表现出该疾病的肌张力障碍患者,7例无法表现出肌张力障碍突变携带者(DYT1和DYT6基因突变)以及8例年龄匹配的正常对照受试者进行了成像,以进行先前的研究。比较了DTI的早期和晚期注册方法。提出了一种超集的早期配准技术,其中将扩散加权图像配准到模板,针对每个对象重新定向梯度矢量,然后将它们组合成张量,然后进行张量计算。超级集包含所有受试者的图像,可用于组比较。我们使用从超集的早期注册中获得的结果,使用确定性纤维跟踪技术对区域进行分组分析。结果:在肌张力障碍突变携带者中,我们在小脑-丘脑-皮质途径中检测到的纤维较少。该结果与以前的研究的结果相吻合,该研究利用概率性束线描记法,并证明基因载体在涉及疾病的途径中具有较少的纤维束。结论:该分析显示了肌张力障碍患者和对照组之间的组水平白质分数各向异性和管道差异,可有助于了解其他非局灶性白质疾病的病理生理。 J.Magn。雷森成像2013; 37:67-75。

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