Abstract

Background: Spinocerebellar ataxia type 3 (SCA) is a cerebellum-dominant degenerative disorder that is characterized primarily by infratentorial damage, although less severe supratentorial involvement may contribute to the clinical manifestation. These impairments may result from the efferent loss of the cerebellar cortex and degeneration of the cerebral cortex.Method: We used the three-dimensional fractal dimension (3D-FD) method to quantify the morphological changes in the supratentorial regions and assessed atrophy in the relatively focal regions in patients with SCA3. A total of 48 patients with SCA3 and 50 sex- and age-matched healthy individuals, as the control group, participated in this study. The 3D-FD method was proposed to distinguish 97 automatic anatomical label regions of gray matter (left cerebrum: 45, right cerebrum: 45, cerebellum: 7) between healthy individuals and patients with SCA3.Results: Patients with SCA3 exhibited reduced brain complexity within both the traditional olivopontocerebellar atrophy (OPCA) pattern and specific supratentorial regions. The study results confirmed the extensive involvement of extracerebellar regions in SCA3. The atrophied regions of SCA3 in infratentorial and supratentorial cortex showed a wide range of overlapped areas as in two functional cortexes, namely cerebellum-related cortex and basal ganglia-related cortex.Conclusions: Our results found that the atrophy of the SCA3 are not only limited in the infratentorial regions. Both cerebellar related cortex and basal ganglia related cortex were affected in the disease process of SCA3. Our findings might correlate to the common symptoms of SCA3, such as ataxia, Parkinsonism, dysarthria, and dysmetria. SCA3 should no longer be considered a disease limited to the cerebellum and its connections; rather, it should be considered a pathology affecting the whole brain.

Highlights

  • Spinocerebellar ataxia type 3 (SCA3) is an inherited neurodegenerative disorder caused by CAG expansion in the coding region of chromosome 14q32.1 [1, 2]

  • The SCA3 disorder has been described as cerebellar cognitive affective syndrome (CCAS) [6, 8]

  • The atrophy of the supratentorial cortex may be the primary factor associated with the dysfunction of the ataxia and Parkinsonism-related regions. These findings suggest that SCA3 should no longer be considered a disease limited to the cerebellum and its connections; rather, it should be considered a pathology affecting the whole brain

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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, 2]. Studies have used positron emission tomography (PET) and single-photon emission computed tomography to identify subclinical abnormalities in the cerebral cortex [13, 14] These studies reported the disruption of the cerebrocerebellar pathway cannot completely explain the cognitive and affective impairment in patients with SCA3. Spinocerebellar ataxia type 3 (SCA) is a cerebellum-dominant degenerative disorder that is characterized primarily by infratentorial damage, less severe supratentorial involvement may contribute to the clinical manifestation. These impairments may result from the efferent loss of the cerebellar cortex and degeneration of the cerebral cortex

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