首页> 外文期刊>American Journal of Neuroradiology >Diffusion Tensor Imaging Detects Abnormalities in the Corticospinal Tracts of Neonates with Infantile Krabbe Disease
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Diffusion Tensor Imaging Detects Abnormalities in the Corticospinal Tracts of Neonates with Infantile Krabbe Disease

机译:扩散张量成像检测出婴儿小儿Krabbe病的皮质脊髓束异常。

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BACKGROUND AND PURPOSE: It is not possible to determine if neonates diagnosed with Krabbe disease through statewide neonate screening programs will develop the disease as infants, juveniles, or adults. The only available treatment for this fatal neurodegenerative condition is unrelated umbilical cord transplantation, but this treatment is only effective before clinical symptoms appear. Therefore, a marker of disease progression is needed. The purpose of this study was to evaluate the use of diffusion tensor imaging (DTI) with fiber tracking in identifying early changes in major motor tracts of asymptomatic neonates with infantile Krabbe disease. MATERIALS AND METHODS: Six neonates with infantile Krabbe disease identified because of family history underwent brain MR imaging within the first 4 weeks of life. Six-direction DTI and quantitative tractography of the corticospinal tracts were performed. Hypothesis tests, 1 for each hemisphere, were used to determine whether the fractional anisotropy (FA) ratio of the neonates with infantile Krabbe disease was significantly different from that of 45 age- and sex-matched controls. RESULTS: The average FA ratio for patients with Krabbe disease was 0.89 and 0.87 for left and right tracts, respectively (P = .002 and < .001). After adjusting for gestational age, gestational age at birth, birth weight, sex, and race, the 6 patients with Krabbe disease had significantly lower FA values than the controls (P < .001). CONCLUSIONS: DTI with quantitative tractography detected significant differences in the corticospinal tracts of asymptomatic neonates who had the early-onset form of Krabbe disease. Once standardized and validated, this tool has the potential to be used as a marker of disease progression in neonates diagnosed through statewide neonate screening programs.
机译:背景与目的:无法通过全州新生儿筛查程序确定婴儿 是否被诊断为克拉伯病,婴儿,青少年或会发展这种疾病。 sup>成人。对于这种致命的神经退行性 病,唯一可用的治疗方法是无关的脐带移植,但是这种 治疗仅在临床症状出现之前有效。 因此,需要疾病进展的标志。 这项研究的目的是评估弥散张量成像 (DTI)和纤维跟踪技术在识别主要 运动系统早期变化中的作用。无症状的婴儿Krabbe 病的新生儿。 材料和方法:6例因家族史而被鉴定的婴儿Krabbe病 的新生儿接受了脑MR成像 在生命的前4周内。进行了皮质脊髓束的六向DTI和定量 造影。假设 测试(每个半球1个)用于确定婴儿 Krabbe病新生儿的 分数各向异性(FA)比是否显着结果与45个年龄 和性别匹配的对照组不同。 结果:Krabbe病 患者的平均FA比为0.89和0.87左侧和右侧(P = .002和<.001)。在调整了胎龄,胎龄,体重,性别和种族的胎龄后,这6名患有Krabbe病的患者的FA值显着降低了 差异, Krabbe病的早期发作形式。通过标准化 并通过验证后,该工具有可能被用作通过全州新生儿筛查程序诊断出的新生儿疾病进展的标志物 。 sup>

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  • 来源
    《American Journal of Neuroradiology》 |2009年第5期|1017-1021|共5页
  • 作者单位

    Program for Neurodevelopmental Function in Rare Disorders at the Center for the Study of Development and Learning, University of North Carolina at Chapel Hill, Chapel Hill, NC;

    FPG Child Development Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC;

    Departments of Radiology, University of North Carolina at Chapel Hill, Chapel Hill, NC;

    Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC;

    Pediatric Blood and Marrow Transplantation Program, Duke University Medical Center, Durham, NC;

    Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC;

    Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC|Computer Science, University of North Carolina at Chapel Hill, Chapel Hill, NC;

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