Gupta A, Poe M D, Styner M A, Panigrahy A, Escolar M L
Program for the Study of Neurodevelopment in Rare Disorders, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Department of Psychiatry, University of North Carolina, Chapel Hill, NC, USA.
Neuroimage Clin. 2014 Sep 26;7:792-8. doi: 10.1016/j.nicl.2014.09.014. eCollection 2015.
Krabbe disease is a fatal neurodegenerative disease caused by rapid demyelination of the central and peripheral nervous systems. The only available treatment, unrelated umbilical cord blood transplantation, is effective only if performed before clinical symptoms appear. Phenotypic expressions of disease-causing mutations vary widely, but genotype-phenotype relationships are unclear. Therefore, we evaluated diffusion tensor imaging (DTI) tractography with volumetric analysis as a biomarker of early white matter changes and functional disability in presymptomatic infants.
We obtained DTI and structural scans of newborns with early-infantile Krabbe disease (n = 9) diagnosed by family history or newborn screening. We compared white matter fiber tract properties to those of normal controls (n = 336) and assessed the ability of tract-based properties to predict longitudinal development in four functional domains (cognitive, fine motor, gross motor, adaptive behavior) after treatment with unrelated umbilical cord blood transplantation. We also assessed the relationship between the standard evaluation (modified Loes score) and DTI results, and the volumetric differences between the Krabbe subjects and normal controls.
Reductions in fractional anisotropy were significant in the corticospinal tract in the Krabbe patients compared to controls, which strongly correlated with motor and cognitive outcomes after transplantation. Significant regional differences were observed in the splenium and uncinate fasciculus in Krabbe patients and these differences correlated only with cognitive outcomes. Regional brain volumes of Krabbe patients were slightly larger than controls. Loes scores did not correlate with DTI results.
Neonatal microstructural abnormalities correlate with neurodevelopmental treatment outcomes in patients treated for infantile Krabbe disease. DTI with quantitative tractography is an excellent biomarker for evaluating infants with Krabbe disease identified through newborn screening.
克拉伯病是一种致命的神经退行性疾病,由中枢和周围神经系统的快速脱髓鞘引起。唯一可用的治疗方法是无关脐血移植,只有在临床症状出现之前进行才有效。致病突变的表型表达差异很大,但基因型与表型的关系尚不清楚。因此,我们评估了扩散张量成像(DTI)纤维束成像结合容积分析,作为症状前婴儿早期白质变化和功能障碍的生物标志物。
我们对通过家族史或新生儿筛查诊断为早发性婴儿克拉伯病的新生儿(n = 9)进行了DTI和结构扫描。我们将白质纤维束特性与正常对照组(n = 336)进行比较,并评估基于纤维束的特性预测无关脐血移植治疗后四个功能领域(认知、精细运动、粗大运动、适应性行为)纵向发育的能力。我们还评估了标准评估(改良洛伊斯评分)与DTI结果之间的关系,以及克拉伯病患者与正常对照组之间的容积差异。
与对照组相比,克拉伯病患者皮质脊髓束的各向异性分数显著降低,这与移植后的运动和认知结果密切相关。在克拉伯病患者的胼胝体和钩束中观察到显著的区域差异,这些差异仅与认知结果相关。克拉伯病患者的区域脑容量略大于对照组。洛伊斯评分与DTI结果无关。
新生儿微观结构异常与婴儿克拉伯病治疗患者的神经发育治疗结果相关。DTI结合定量纤维束成像对于评估通过新生儿筛查确诊的克拉伯病婴儿是一种极好的生物标志物。