Abstract

In addition to cerebellar degeneration symptoms, patients with spinocerebellar ataxia type 3 (SCA3) exhibit extensive involvements with damage in the prefrontal cortex. A network model has been proposed for investigating the structural organization and functional mechanisms of clinical brain disorders. For neural degenerative diseases, a cortical feature-based structural connectivity network can locate cortical atrophied regions and indicate how their connectivity and functions may change. The brain network of SCA3 has been minimally explored. In this study, we investigated this network by enrolling 48 patients with SCA3 and 48 healthy subjects. A novel three-dimensional fractal dimension-based network was proposed to detect differences in network parameters between the groups. Copula correlations and modular analysis were then employed to categorize and construct the structural networks. Patients with SCA3 exhibited significant lateralized atrophy in the left supratentorial regions and significantly lower modularity values. Their cerebellar regions were dissociated from higher-level brain networks, and demonstrated decreased intra-modular connectivity in all lobes, but increased inter-modular connectivity in the frontal and parietal lobes. Our results suggest that the brain networks of patients with SCA3 may be reorganized in these regions, with the introduction of certain compensatory mechanisms in the cerebral cortex to minimize their cognitive impairment syndrome.

Highlights

  • Spinocerebellar ataxia type 3 (SCA3) is an inherited neurodegenerative disorder caused by CAG expansion in the coding region of chromosome 14q32.1 [1]

  • Patients with SCA3 exhibited significant lateralized atrophy in the left supratentorial regions, the occipital and temporal lobes that were all in the left hemisphere

  • We found that brain regions included in Module I of the control group’s brain networks were grouped into two modules, namely Modules I and IV, in the SCA3 group

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Summary

Introduction

Spinocerebellar ataxia type 3 (SCA3) is an inherited neurodegenerative disorder caused by CAG expansion in the coding region of chromosome 14q32.1 [1]. Patients with SCA3 exhibit cerebellar syndrome, including ataxia of gait, dysarthria, dysmetria, nystagmus, peripheral neuropathy, and pyramidal and extrapyramidal manifestations [2]. These patients exhibit cognitive impairment and emotional deficits, which may be caused by cerebellar and cerebral cortex atrophy [3]. The mature human brain is both structurally and functionally specialized, such that discrete areas of the cerebral cortex perform distinct types of information processing [4]. A modular network with graph theory can provide further quantitative insight into the organization of complex brain networks and their regional connections [7]

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