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延髓起病和肢体起病的肌萎缩侧索硬化症的弥散张量成像模式存在差异。

Diffusion tensor imaging patterns differ in bulbar and limb onset amyotrophic lateral sclerosis.

作者信息

Prell Tino, Peschel Thomas, Hartung Viktor, Kaufmann Joern, Klauschies Ribanna, Bodammer Nils, Kollewe Katja, Dengler Reinhard, Grosskreutz Julian

机构信息

Hans-Berger Department of Neurology, Jena University Hospital, Erlanger Allee 101, 07747 Jena, Germany.

出版信息

Clin Neurol Neurosurg. 2013 Aug;115(8):1281-7. doi: 10.1016/j.clineuro.2012.11.031. Epub 2012 Dec 23.

Abstract

BACKGROUND

Amyotrophic lateral sclerosis (ALS) is characterized by pronounced clinical heterogeneity in terms of onset and disease progression. Widespread changes in white matter fibres could be observed by diffusion tensor imaging (DTI), which detects alterations in the degree (diffusivity, ADC) and directedness (fractional anisotropy, FA) of proton movement. The aim of the current study was to determine whether different ALS onset types were reflected in different DTI brain patterns.

METHODS

Seventeen patients with a diagnosis of ALS (6 bulbar, 11 limb onset) and seventeen age-matched controls received 1.5T DTI, where FA and ADC were analyzed using statistical parametric mapping.

RESULTS

In ALS patients, an increased diffusivity in the white matter was found below the precentral gyrus and along the corticospinal tract (CST) right into the internal capsule. The FA was decreased in the posterior limb of internal capsule and in the subcortical white matter in the precentral gyrus. In bulbar onset increased diffusivity was found in the CST, whilst in limb onset, frontal subcortical areas displayed an increased diffusivity.

CONCLUSION

DTI changes can be regarded as prominent features in ALS. Herein we were able to demonstrate discriminating brain DTI patterns due to bulbar or limb onset.

摘要

背景

肌萎缩侧索硬化症(ALS)在发病和疾病进展方面具有明显的临床异质性。通过扩散张量成像(DTI)可以观察到白质纤维的广泛变化,DTI可检测质子运动程度(扩散率,ADC)和方向性(分数各向异性,FA)的改变。本研究的目的是确定不同的ALS发病类型是否反映在不同的DTI脑图谱中。

方法

17例诊断为ALS的患者(6例延髓起病,11例肢体起病)和17例年龄匹配的对照者接受了1.5T DTI检查,使用统计参数映射分析FA和ADC。

结果

在ALS患者中,中央前回下方和沿皮质脊髓束(CST)直至内囊的白质扩散率增加。内囊后肢和中央前回皮质下白质的FA降低。在延髓起病的患者中,CST扩散率增加,而在肢体起病的患者中,额叶皮质下区域扩散率增加。

结论

DTI变化可被视为ALS的突出特征。在此我们能够证明由于延髓或肢体起病导致的脑DTI图谱差异。

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