Kim Hee-Jin, de Leon Mony, Wang Xiuyuan, Kim Hyun Young, Lee Young-Jun, Kim Yeon-Ha, Kim Seung Hyun
Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea.
Center for Brain Health, Department of Psychiatry, NYU School of Medicine, New York, New York, United States of America.
PLoS One. 2017 Jan 17;12(1):e0168424. doi: 10.1371/journal.pone.0168424. eCollection 2017.
Amyotrophic lateral sclerosis (ALS) is a rapidly progressing, phenotypically heterogeneous neurodegenerative disease affecting mainly the motor neuron system. The present voxel-based morphometry (VBM) study investigated whether patterns of brain atrophy differ among sporadic ALS subtypes.
Sporadic ALS patients (n = 62) with normal cognition and age-matched healthy controls (n = 57) were included in the study. ALS patients were divided into limb- and bulbar-onset groups according to clinical manifestations at symptom onset (n = 48 and 14, respectively). Clinical measures were ALS Functional Rating Scale-Revised (ALSFRS-R) score, disease duration, and forced vital capacity (FVC). Patterns of brain atrophy between ALS subgroups were compared by VBM.
In limb-onset ALS patients, atrophy was largely confined to the motor cortex and adjacent pre- and postcentral regions. However, in the bulbar-onset group, affected regions were more widespread and included these same areas but also extended to the bilateral frontotemporal and left superior temporal and supramarginal gyri, and multiple regression analysis revealed that their ALSFRS-R scores were associated with extensive loss of gray matter while FVC was related to atrophy in subcortical regions of the left superior temporal gyrus. In limb-onset ALS patients, disease duration was related to the degree of atrophy in the motor and adjacent areas.
Sporadic ALS subtypes show different patterns of brain atrophy. Neural networks related to limb and bulbar motor functions in each ALS subtype may underlie their distinct patterns of cerebral atrophy. That is, more extensive cortical and subcortical atrophy is correlated with greater ALSFRS-R severity and shorter disease duration in the bulbar-onset subtype and may explain the poor prognosis of these patients.
肌萎缩侧索硬化症(ALS)是一种进展迅速、表型异质性的神经退行性疾病,主要影响运动神经元系统。本基于体素的形态学测量(VBM)研究调查了散发性ALS亚型之间脑萎缩模式是否存在差异。
本研究纳入了认知正常的散发性ALS患者(n = 62)和年龄匹配的健康对照者(n = 57)。ALS患者根据症状发作时的临床表现分为肢体起病组和延髓起病组(分别为n = 48和14)。临床测量指标为ALS功能评定量表修订版(ALSFRS-R)评分、病程和用力肺活量(FVC)。通过VBM比较ALS亚组之间的脑萎缩模式。
在肢体起病的ALS患者中,萎缩主要局限于运动皮层以及相邻的中央前回和中央后回区域。然而,在延髓起病组中,受影响区域更为广泛,包括上述相同区域,但也扩展至双侧额颞叶、左侧颞上回和缘上回,多元回归分析显示,他们的ALSFRS-R评分与广泛的灰质丢失有关,而FVC与左侧颞上回皮质下区域的萎缩有关。在肢体起病的ALS患者中,病程与运动及相邻区域的萎缩程度有关。
散发性ALS亚型表现出不同的脑萎缩模式。每个ALS亚型中与肢体和延髓运动功能相关的神经网络可能是其不同脑萎缩模式的基础。也就是说,更广泛的皮质和皮质下萎缩与延髓起病亚型中更高的ALSFRS-R严重程度和更短的病程相关,这可能解释了这些患者预后较差的原因。