Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and Duration.

IF 2.7 3区 医学 Q3 NEUROSCIENCES
Cerebellum Pub Date : 2024-08-01 Epub Date: 2024-02-16 DOI:10.1007/s12311-024-01659-0
Mónica Ferreira, Tamara Schaprian, David Kügler, Martin Reuter, Katharina Deike-Hoffmann, Dagmar Timmann, Thomas M Ernst, Paola Giunti, Hector Garcia-Moreno, Bart van de Warrenburg, Judith van Gaalen, Jeroen de Vries, Heike Jacobi, Katharina Marie Steiner, Gülin Öz, James M Joers, Chiadi Onyike, Michal Povazan, Kathrin Reetz, Sandro Romanzetti, Thomas Klockgether, Jennifer Faber
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引用次数: 0

Abstract

Cerebellar atrophy is the neuropathological hallmark of most ataxias. Hence, quantifying the volume of the cerebellar grey and white matter is of great interest. In this study, we aim to identify volume differences in the cerebellum between spinocerebellar ataxia type 1 (SCA1), SCA3 and SCA6 as well as multiple system atrophy of cerebellar type (MSA-C). Our cross-sectional data set comprised mutation carriers of SCA1 (N=12), SCA3 (N=62), SCA6 (N=14), as well as MSA-C patients (N=16). Cerebellar volumes were obtained from T1-weighted magnetic resonance images. To compare the different atrophy patterns, we performed a z-transformation and plotted the intercept of each patient group's model at the mean of 7 years of ataxia duration as well as at the mean ataxia severity of 14 points in the SARA sum score. In addition, we plotted the extrapolation at ataxia duration of 0 years as well as 0 points in the SARA sum score. Patients with MSA-C demonstrated the most pronounced volume loss, particularly in the cerebellar white matter, at the late time intercept. Patients with SCA6 showed a pronounced volume loss in cerebellar grey matter with increasing ataxia severity compared to all other patient groups. MSA-C, SCA1 and SCA3 showed a prominent atrophy of the cerebellar white matter. Our results (i) confirmed SCA6 being considered as a pure cerebellar grey matter disease, (ii) emphasise the involvement of cerebellar white matter in the neuropathology of SCA1, SCA3 and MSA-C, and (iii) reflect the rapid clinical progression in MSA-C.

Abstract Image

共济失调的小脑体积测量:共济失调严重程度与持续时间的关系
小脑萎缩是大多数共济失调症的神经病理学特征。因此,量化小脑灰质和白质的体积非常重要。在这项研究中,我们旨在确定脊髓小脑共济失调 1 型(SCA1)、SCA3 和 SCA6 以及小脑型多系统萎缩(MSA-C)之间的小脑体积差异。我们的横断面数据集包括SCA1(12人)、SCA3(62人)、SCA6(14人)突变携带者以及MSA-C患者(16人)。小脑体积由T1加权磁共振图像获得。为了比较不同的萎缩模式,我们进行了z变换,并绘制了每组患者在共济失调持续时间平均为7年以及共济失调严重程度平均为SARA总分14分时的模型截距图。此外,我们还绘制了共济失调持续时间为 0 年以及 SARA 总分为 0 分时的外推法。MSA-C患者在晚期时间截断时表现出最明显的体积损失,尤其是小脑白质。与所有其他患者组相比,随着共济失调严重程度的增加,SCA6 患者的小脑灰质体积明显缩小。MSA-C、SCA1 和 SCA3 显示小脑白质显著萎缩。我们的研究结果(i)证实了 SCA6 被认为是一种纯粹的小脑灰质疾病,(ii)强调了小脑白质参与了 SCA1、SCA3 和 MSA-C 的神经病理学,(iii)反映了 MSA-C 的快速临床进展。
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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.
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