Global and Regional Brain Grey and White Matter Morphometry Alterations in Type 1, 2, and 3 Spinocerebellar Ataxias (SCAs) Patients.

IF 2.7 3区 医学 Q3 NEUROSCIENCES Cerebellum Pub Date : 2024-12-07 DOI:10.1007/s12311-024-01760-4
Runhua Sha, Shu Su, Manshi Hu, Ling Ma, Huasong Cai, Chao Wu, Jing Zhao
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Abstract

Spinocerebellar ataxias (SCAs) types 1, 2, and 3 are the most common subtypes of SCAs. However, the atrophy patterns of these three subtypes still need to be fully clarified. In this study, a total of 130 genetically confirmed SCA patients (SCA1: n = 16; SCA2: n = 13; symptomatic SCA3: n = 76; pre-symptomatic SCA3: n = 25) along with 65 age- and sex-matched healthy controls (HCs) were enrolled. MR volumetric analysis was used to explore the different atrophied patterns in these three SCA subtypes and the associations between significant morphometry alterations and clinical variables were further analyzed. Compared with HCs, the global brain grey matter (GM) of the three SCA subtypes and white matter (WM) volumes of the SCA2 and SCA3 were significantly reduced. SCA2 had significantly more severe GM volume atrophy than symptomatic SCA3. For local GM and WM volumes, all three subtypes of SCA have significant atrophy in infra- and supratentorial areas than HCs. The pre-symptomatic SCA3 patients had already demonstrated substantial WM atrophy. The SCAs subgroup comparisons showed that compared with symptomatic SCA3, SCA1 and SCA2 demonstrated more severe atrophy in regions of the cerebral and cerebellum, but symptomatic SCA3 had significantly atrophied bilateral lenticular nuclei. Besides, no significant difference was found in the local GM or WM volume between SCA1 and SCA2. Furthermore, some affected GM and WM regions, especially the damaged cerebellar peduncles, showed significant correlations with disease duration and severity in SCA1 and symptomatic SCA3. Our research results indicate differences in MRI brain injury patterns among common SCA subtypes, which might shed light on the deeper understanding of the pathophysiological mechanisms of SCAs.

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1、2、3型脊髓小脑共济失调(SCAs)患者脑灰质和白质形态的整体和局部改变
脊髓小脑共济失调(SCAs) 1、2和3型是SCAs最常见的亚型。然而,这三种亚型的萎缩模式仍然需要充分澄清。本研究共纳入130例经基因证实的SCA患者(SCA1: n = 16;SCA2: n = 13;症状性SCA3: n = 76;症状前SCA3: n = 25)以及65名年龄和性别匹配的健康对照(hc)入组。磁共振体积分析探讨了这三种SCA亚型的不同萎缩模式,并进一步分析了显著形态改变与临床变量之间的关系。与hcc相比,三种SCA亚型的全脑灰质(GM)和SCA2、SCA3的白质(WM)体积均显著减少。SCA2的GM体积萎缩明显比有症状的SCA3严重。对于局部GM和WM体积,所有三种SCA亚型在幕下和幕上区域都比hcc有明显的萎缩。症状前的SCA3患者已经表现出明显的WM萎缩。SCAs亚组比较显示,与症状性SCA3相比,SCA1和SCA2在大脑和小脑区域表现出更严重的萎缩,但症状性SCA3的双侧晶状体核明显萎缩。此外,SCA1和SCA2的局部GM和WM体积无显著差异。此外,一些受影响的GM和WM区域,特别是受损的小脑蒂,在SCA1和症状性SCA3中显示出与疾病持续时间和严重程度的显著相关性。我们的研究结果表明,常见SCA亚型的MRI脑损伤模式存在差异,这可能有助于更深入地了解SCA的病理生理机制。
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来源期刊
Cerebellum
Cerebellum 医学-神经科学
CiteScore
6.40
自引率
14.30%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Official publication of the Society for Research on the Cerebellum devoted to genetics of cerebellar ataxias, role of cerebellum in motor control and cognitive function, and amid an ageing population, diseases associated with cerebellar dysfunction. The Cerebellum is a central source for the latest developments in fundamental neurosciences including molecular and cellular biology; behavioural neurosciences and neurochemistry; genetics; fundamental and clinical neurophysiology; neurology and neuropathology; cognition and neuroimaging. The Cerebellum benefits neuroscientists in molecular and cellular biology; neurophysiologists; researchers in neurotransmission; neurologists; radiologists; paediatricians; neuropsychologists; students of neurology and psychiatry and others.
期刊最新文献
Emerging Deep Brain Stimulation Targets in the Cerebellum for Tremor. Assessment of Peripheral Neuropathy Using Current Perception Threshold Measurement in Patients with Spinocerebellar Ataxia Type 3. Tremor in the Age of Omics: An Overview of the Transcriptomic Landscape of Essential Tremor. Spontaneous Nystagmus Violating the Alexander's Law: Neural Substrates and Mechanisms. Causally Mapping the Cerebellum in Children and Young Adults: from Motor to Cognition.
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