Brain structural changes in alternating hemiplegia of childhood using single-case voxel-based morphometry analysis

IF 1.7 4区 医学 Q3 DEVELOPMENTAL BIOLOGY
Elly Arizono, Noriko Sato, Yoko Shigemoto, Yukio Kimura, Emiko Chiba, Hiroyuki Maki, Hiroshi Matsuda, Eri Takeshita, Yuko Shimizu-Motohashi, Masayuki Sasaki, Kazuhiro Saito
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Abstract

Background and purpose

Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disease caused by ATP1A3 mutations. Using voxel-based morphometry (VBM) analysis, we compared an AHC patient cohort with controls. Additionally, with single-case VBM analysis, we assessed the associations between clinical severity and brain volume in patients with AHC.

Materials and methods

To investigate structural brain changes in gray matter (GM) and white matter (WM) volumes between 9 patients with AHC and 20 age-matched controls, VBM analysis was performed using three-dimensional T1-weighted magnetic resonance imaging. Single-case VBM analysis was also performed on nine patients with AHC to investigate the associations between the respective volumes of GM/WM differences and the motor level, cognitive level, and status epilepticus severity in patients with AHC.

Results

Compared with controls, patients with AHC showed significant GM volume reductions in both hippocampi and diffuse cerebellum, and there were WM reductions in both cerebral hemispheres. In patients with AHC, cases with more motor dysfunction, the less GM/WM volume of cerebellum was shown. Three of the six cases with cognitive dysfunction showed a clear GM volume reduction in the insulae. Five of the six cases with status epilepticus showed the GM volume reduction in hippocampi. One case had severe status epilepticus without motor dysfunction and showed no cerebellar atrophy.

Conclusion

With single-case VBM analysis, we could show the association between region-specific changes in brain volume and the severity of various clinical symptoms even in a small sample of subjects.

Abstract Image

应用基于体素的单例形态计量学分析儿童交替性偏瘫的脑结构变化。
背景与目的:儿童交替性偏瘫(AHC)是一种罕见的由ATP1A3突变引起的神经发育疾病。使用基于体素的形态计量学(VBM)分析,我们将AHC患者队列与对照组进行了比较。此外,通过单例VBM分析,我们评估了AHC患者的临床严重程度与脑容量之间的关系。材料和方法:为了研究9名AHC患者和20名年龄匹配的对照组之间灰质(GM)和白质(WM)体积的大脑结构变化,使用三维T1加权磁共振成像进行VBM分析。对9例AHC患者进行了单例VBM分析,以研究GM/WM差异的体积与AHC患者的运动水平、认知水平和癫痫持续状态严重程度之间的关系。结果:与对照组相比,AHC患者海马和弥漫性小脑的GM体积均显着减少,并且两个大脑半球的WM均减少。在AHC患者中,运动功能障碍越多,小脑的GM/WM体积越小。6例认知功能障碍患者中有3例显示脑岛GM体积明显减少。6例癫痫持续状态患者中有5例海马GM体积减少。1例患者出现严重癫痫持续状态,无运动功能障碍,无小脑萎缩。结论:通过单例VBM分析,即使在小样本受试者中,我们也可以显示脑容量的区域特异性变化与各种临床症状的严重程度之间的关系。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: International Journal of Developmental Neuroscience publishes original research articles and critical review papers on all fundamental and clinical aspects of nervous system development, renewal and regeneration, as well as on the effects of genetic and environmental perturbations of brain development and homeostasis leading to neurodevelopmental disorders and neurological conditions. Studies describing the involvement of stem cells in nervous system maintenance and disease (including brain tumours), stem cell-based approaches for the investigation of neurodegenerative diseases, roles of neuroinflammation in development and disease, and neuroevolution are also encouraged. Investigations using molecular, cellular, physiological, genetic and epigenetic approaches in model systems ranging from simple invertebrates to human iPSC-based 2D and 3D models are encouraged, as are studies using experimental models that provide behavioural or evolutionary insights. The journal also publishes Special Issues dealing with topics at the cutting edge of research edited by Guest Editors appointed by the Editor in Chief. A major aim of the journal is to facilitate the transfer of fundamental studies of nervous system development, maintenance, and disease to clinical applications. The journal thus intends to disseminate valuable information for both biologists and physicians. International Journal of Developmental Neuroscience is owned and supported by The International Society for Developmental Neuroscience (ISDN), an organization of scientists interested in advancing developmental neuroscience research in the broadest sense.
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