Abstract

Structural MR imaging does not enable reliable differentiation of spinocerebellar ataxia (SCA) types 1 and 2 (SCA1 and SCA2), and imaging may be normal during the first years after the onset of symptoms. We aimed at determining whether measurements of the apparent diffusion coefficient (ADC) and fractional anisotropy (FA) may enable their differentiation. We enrolled 14 patients with SCA1, 11 with SCA2, and 9 age-matched controls. Diffusion tensor imaging (DTI) was performed on a 1.5T scanner, with b = 1000s/mm2 and 12 directions. ADC and FA were measured by means of regions of interest, positioned in the corticospinal tract at the level of the cerebral peduncle and at the level of the pons, in the transverse pontine fibers, in the superior and middle cerebellar peduncle, and in the hemispheric cerebellar white matter. With respect to controls, the ADC was significantly elevated in the middle cerebellar peduncle and in hemispheric white matter in SCA1, and in all regions under consideration in SCA2. It was significantly higher in SCA2 than in SCA1 in all regions under consideration. With respect to controls, the FA was significantly reduced in all regions under consideration in SCA1 and in SCA2. It was significantly lower in SCA2 than in SCA1 in the transverse pontine fibers and in the corticospinal tract at the level of the cerebral peduncle. Correlations with clinical scores were found. DTI did not enable differentiation between SCA1 and SCA2. However, strongly significant differences between the 2 subtypes and with respect to controls and correlations with clinical scores were found.

Highlights

  • MethodsWe enrolled 14 patients with SCA1, 11 with SCA2, and 9 age-matched controls

  • AND PURPOSE: Structural MR imaging does not enable reliable differentiation of spinocerebellar ataxia (SCA) types 1 and 2 (SCA1 and SCA2), and imaging may be normal during the first years after the onset of symptoms

  • With respect to controls, the apparent diffusion coefficient (ADC) was significantly elevated in the middle cerebellar peduncle and in hemispheric white matter in SCA1, and in all regions under consideration in SCA2

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Summary

Methods

We enrolled 14 patients with SCA1, 11 with SCA2, and 9 age-matched controls. Fourteen patients with SCA1 (4 female and male, age 48.5 Ϯ 11.3 years) and patients with SCA2 CAG repeats (range) Age at onset (years) Disease duration (years) Dysarthria (%) Nystagmus (%) Vertical gaze palsy (%) Horizontal gaze palsy (%) Slow saccades (%) Increased bicep reflexes (%) Increased patellar reflexes (%) Lower limb spasticity (%) Babinski sign (%) Decreased vibration sense (%) Dysphagia (%) Amyotrophy (%) Cognitive impairment (%) Sphincteric disturbances (%) SCA1 (n ϭ 14). Years) were scanned as part of a locally approved multicentric study.[18] We obtained written informed consent from all participants, in accordance with institutional guidelines and with the Helsinki declaration

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