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首页> 外文期刊>AJNR. American journal of neuroradiology >Tract-based spatial statistical analysis of diffusion tensor imaging in pediatric patients with mitochondrial disease: Widespread reduction in fractional anisotropy of white matter tracts
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Tract-based spatial statistical analysis of diffusion tensor imaging in pediatric patients with mitochondrial disease: Widespread reduction in fractional anisotropy of white matter tracts

机译:儿科线粒体疾病患者基于张量的弥散张量成像的空间统计分析:白质束分数各向异性的广泛降低

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摘要

BACKGROUND AND PURPOSE: Often diagnosed at birth or in early childhood, mitochondrial disease presents with a variety of clinical symptoms, particularly in organs and tissues that require high energetic demand such as brain, heart, liver, and skeletal muscles. In a group of pediatric patients identified as having complex I or I/III deficits on muscle biopsy but with white matter tissue appearing qualitatively normal for age, we hypothesized that quantitative DTI analyses might unmask disturbance in microstructural integrity. MATERIALS AND METHODS: In a retrospective study, DTI and structural MR brain imaging data from 10 pediatric patients with confirmed mitochondrial disease and 10 clinical control subjects were matched for age, sex, scanning parameters, and date of examination. Paired TBSS was performed to evaluate differences in FA, MD, and the separate diffusion direction terms (λr and λa). RESULTS: In patients with mitochondrial disease, significant widespread reductions in FA values were shown in white matter tracts. Mean diffusivity values were significantly increased in patients, having a sparser distribution of affected regions compared with FA. Separate diffusion maps showed significant increase in λr and no significant changes in λa. CONCLUSIONS: Despite qualitatively normal-appearing white matter tissues, patients with complex I or I/III deficiency have widespread microstructural changes measurable with quantitative DTI.
机译:背景与目的:线粒体疾病通常在出生时或儿童早期被诊断出,具有多种临床症状,特别是在需要高能量需求的器官和组织(例如脑,心脏,肝脏和骨骼肌)中。在一组确定为肌肉活检具有复杂I或I / III缺陷但白质组织在年龄上定性正常的儿科患者中,我们假设定量DTI分析可能掩盖了微结构完整性的紊乱。材料与方法:在一项回顾性研究中,对10例确诊线粒体疾病的儿科患者和10例临床对照受试者的DTI和MR脑结构成像数据进行了年龄,性别,扫描参数和检查日期的匹配。配对TBSS用于评估FA,MD和单独的扩散方向项(λr和λa)的差异。结果:在线粒体疾病患者中,白质区显示出FA值显着广泛降低。与FA相比,患者的平均扩散率值显着增加,受影响区域的分布较稀疏。单独的扩散图显示λr显着增加,而λa没有显着变化。结论:尽管白质组织的外观定性正常,但患有复杂的I或I / III缺乏症的患者仍有广泛的微观结构变化,可通过定量DTI进行测量。

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