Vol. 10 nº 4 - Oct/Nov/Dec de 2016
Original Article Pages 310 to 314

Cognitive impairment in Spinocerebellar ataxia type 10
Comprometimento cognitivo na ataxia Espinocerebelar do tipo 10

Authors: Adriana Moro1; Hélio Afonso Ghizoni Teive2


Descriptors: spinocerebellar ataxia type 10, cognitive dysfunction, psychiatric, neuropsychological.
ataxia espinocerebelar do tipo 10, disfunção cognitiva, psiquiátrica, neuropsicológica.

BACKGROUND: Cognitive and psychiatric dysfunction has been described in several neurodegenerative diseases but has not been systematically evaluated in spinocerebellar ataxia type 10 (SCA10).
OBJECTIVE: The aim of the present study was to investigate the core cognitive features in a large cohort of Brazilian patients with SCA10, comparing the results against a healthy control group.
METHODS: Twenty-eight SCA10 and 28 healthy subjects were prospectively assessed regarding cognitive function and psychiatric disorders at the Movement Disorders Unit of the Federal University of Paraná between February 2012 and October 2014.
RESULTS: The SCA10 group had worse depression scores, as well as cognitive performance, when compared to healthy individuals.
CONCLUSION: Our study showed mild cognitive and mood dysfunctions in patients with SCA10, consistent with the symptoms reported in the Cerebellar Cognitive Affective Syndrome described by Schmahmann JD in 1998. The description of these findings is an important clinical phenomenon that may guide physicians in specific disease management and improve quality of life of these patients.

EMBASAMENTO: Disfunção cognitiva e psiquiátrica tem sido descrita em diversas doenças neurodegenerativas, entretanto, até o momento não foi sistematicamente avaliada na ataxia espinocerebelar do tipo 10 (AEC10).
OBJETIVO: O objetivo do presente estudo foi investigar as principais características cognitivas em uma grande coorte brasileira de pacientes com AEC10, comparando com um grupo controle saudável.
MÉTODOS: Vinte e oito pacientes com AEC10 e 28 indivíduos saudáveis foram avaliados prospectivamente em relação a função cognitiva e distúrbios psiquiátricos na Unidade de Distúrbios do Movimento da Universidade Federal do Paraná, de fevereiro de 2012 a outubro de 2014.
RESULTADOS: O grupo de pacientes com AEC10 apresentou piores escores de depressão, assim como pior desempenho cognitivo, quando comparado aos indivíduos saudáveis.
CONCLUSÃO: Nosso estudo demonstrou disfunções leves de humor e cognição nos pacientes com AEC10, consistentes com os sintomas relatados na Síndrome Cerebelar Cognitivo Afetiva, descrita por Schmahmann em 1998. A descrição desses achados é um fenômeno clínico importante que pode guiar os médicos assistentes no manejo específico da doença e melhorar a qualidade de vida desses pacientes.


Spinocerebellar ataxias (SCA) are a large and complex heterogeneous group of autosomal dominant degenerative disorders characterized by progressive degeneration of the cerebellum and its afferent and efferent connections. Other nervous system structures are typically affected, including the basal ganglia, brainstem nuclei, pyramidal tracts, posterior column and anterior horn of the spinal cord, and peripheral nerves.1-6

The wide range of clinical manifestations in SCAs include cerebellar gait and limb ataxia, with dysmetria, dysdiadochokinesia, intention tremor, dysarthria, and nystagmus; in addition, patients may have extracerebellar signs, such as dementia, epilepsy, visual disorders, peripheral neuropathy, ophthalmoplegia, pyramidal signs, and movement disorders, including parkinsonism, dystonia, myoclonus, and chorea.1-6 The prevalence and severity of cognitive dysfunction vary considerably in SCA populations.7 Significant impairments on verbal memory and fronto-executive tasks have been described in SCA1, SCA2 and SCA3 patients in recent years.8,9 More rarely, cognitive deficits and dementia have also been found in SCA12, 17, 19 and 21, as well as in dentatorubral-pallidoluysian atrophy (DRPLA).10-14

Spinocerebellar ataxia type 10 (SCA10) is a rare, dominantly inherited neurodegenerative disorder caused by a pentanucleotide (ATTCT) repeat expansion in intron 9 of the ATXN10 gene on chromosome 22q13.3. The ATTCT repeat is polymorphic, ranging in size from 10 to 32 repeats in the normal population, and from 800 to 4500 in mutant alleles.15 Reduced penetrance has been found for intermediate size alleles of 280-850 repeats.16

Rasmussen et al.17 published a seminal study involving the clinical and genetic analysis of 18 patients from 4 Mexican families with SCA10. Clinical data, besides cerebellar ataxia and epilepsy - found in 72.2% of the cases - also included sensory polyneuropathy, pyramidal signs, cognitive and neuropsychiatric impairment. Nevertheless, a large series from Brazil including 60 patients described ataxia as the sole manifestation, with seizures detected at a frequency similar to that expected for the general population.18 Neuropsychological tests were normal in this series of patients, except in one patient who had a low IQ of 73 and mild memory impairment.

Despite growing research on the cognitive aspects of cerebellar disorders, there are scant data establishing the cognitive pattern in patients with a genetic diagnosis of SCA10. The aim of the present study was to investigate the core cognitive features in a large cohort of Brazilian patients, comparing the results with a healthy control group.


A total of 28 controls and 28 SCA10 patients from 14 unrelated families were evaluated at the Movement Disorders Unit of the Federal University of Paraná between February 2012 and October 2014. The Unit is a major referral center for SCAs in southern Brazil. Age- and sex-matched healthy volunteers, recruited among nonconsanguineous individuals (spouses or caregivers), were invited to participate. This study was approved by the Institutional Ethics Committee of the Federal University of Paraná and all patients and healthy controls signed an informed consent form.

Neurological and psychiatric evaluation. The ataxia clinical assessment was conducted in all subjects using the Brazilian validated scale for the assessment and rating of ataxia (SARA).19 Symptoms of depression were evaluated using the Beck Depression Inventory (BDI),20 and symptoms of anxiety were assessed using the Hamilton Anxiety Rating Scale (HAM-A).21

Neuropsychological assessment. The Brazilian version of the Mini-Mental State Examination (MMSE)22 was used as a screening tool for general intellectual abilities. Executive functions were evaluated with the Frontal Assessment Battery (FAB).23 Semantic verbal fluency (animals) and phonemic (nouns beginning with the letter S) tests were used to assess association fluency, and the Clock Drawing Test (CDT)24 was used to screen for visuospatial and constructional abilities based on a scoring system from 0 to 15.

Statistical analysis. Statistical comparisons were conducted using STATA software (StataCorp LP, Texas, USA, http://www.stata.com/). The distribution of all continuous variables was assessed using the Shapiro-Wilk and Shapiro-Francia tests for normality. To compare the means and medians, Student's t and Wilcoxon-Mann-Whitney tests were used, respectively. The chi-square test and the Fisher exact test were also used for analysis of binomial variables. Spearman's rank correlation coefficient was used to compare cognitive variables with disease duration and SARA, as well as the impact of depressive symptoms on performance in cognitive tests. Differences were considered significant when p was <0.05.


Among the patients with SCA10, mean age was 46.8 11.6 years, mean age at disease onset was 31.7 7.6 years and mean disease duration was 15.5 12 years. Regarding ataxia evaluation, the mean score on the SARA was 9.9 4.5. The median of ATTCT repetition length was 1990 (1900-2229). For detailed characteristics, see Table 1.

Depressive symptoms were evaluated using the BDI, revealing a median of 12.5 (IR 8.0-19.5) in patients with SCA10 and 5 (IR 3-10) in controls (p=0.008). The HAM-A was used to assess the presence of anxiety, showing a median of 8.5 (IR 4-17) in SCA10 patients and 7 (IR 4-10) in controls.

Table 2 shows a comparison of the neuropsychological tests performed, as well as the psychiatric evaluation. In all cognitive tests - FAB, semantic verbal fluency, phonemic verbal fluency and CDT - the performance of healthy controls was better than that of SCA10 patients.

Spearman's rank correlation coefficient showed no correlation between SARA and cognitive deficit, as there was no correlation between disease duration and cognitive impairment. Correlation between depression and the cognitive performance of SCA10 patients was also assessed where worse results on the CDT were found in patients with higher BDI scores, suggesting that depressive symptoms may have negatively impacted patient performance (Table 3).


In this study, we described impairment of visuospatial abilities, executive functions and verbal fluency in a large cohort of patients with SCA10. Previous studies involving patients with SCA10 performed a less detailed analysis of the neuropsychological changes. Rasmussen et al. showed a below-normal IQ in the majority of the patients, in addition to mood disorders consisting of depression, aggression, or both, in 10 out of 18 SCA10 patients analyzed.17 Trikamji et al. recently reported a Hispanic family which presented with SCA and paranoid schizophrenia. Two children had a history of psychosis, depression and paranoid delusions with auditory hallucinations.25 The authors supported the evidence for cerebellar association with schizophrenia in particular, with neuroimaging studies showing reduction in the volume of the cerebellar vermis and bilateral cerebellar hemispheres in schizophrenics. Furthermore, a decrease in the size and density of Purkinje cells were noted, and abnormal cerebellar blood flow on functional imaging was also reported.25

A possible explanation for cognitive impairment in SCA10 patients is disruption of cerebellar modulation of neural circuits. The Cerebellar Cognitive Affective Syndrome (CCAS) is a well-known condition, characterized by disturbances in executive function, spatial cognition, language and emotional regulation of behavior.26 CCAS involves neural circuits linking prefrontal, posterior parietal, superior temporal, and limbic cortices with the cerebellum.26 Moreover, functional imaging studies demonstrating evidence of activation of the cerebellum during a memory task and verbal fluency task reflect this close functional relationship.27,28

The presence of cognitive dysfunction has been studied in various types of SCAs, particularly SCA3 due to its higher frequency worldwide. Bürk et al. studied the cognitive deficits in 36 patients and a control group of 8 patients. The authors found prominent executive dysfunction in SCA1, and mild deficits of verbal memory in SCA1, SCA2 and SCA3.9 The authors also stated that the cognitive deficits found could have stemmed from disruption in the cerebrocerebellar circuitry, probably at the pontine level.9 A study performed with SCA2 patients showed that 25% of patients had dementia and there was also evidence of verbal memory and executive dysfunction in non-demented subjects.29 Kawai et al., studied 13 genetically confirmed SCA6 patients using neuropsychological tests and brain SPECT, and found prefrontal hypoperfusion and cognitive dysfunction in these patients.30

As expected, the prevalence of mood disorders in patients with spinocerebellar ataxia was higher than estimates for healthy control, and median score of BDI was higher in the SCA10 group. Depressive symptoms are very common and significantly impair the subjective well-being of ataxic patients.31 A survey performed in 526 SCA patients from the European Integrated Project on Spinocerebellar Ataxias (EUROSCA) clinical group, found that 46% of patients exhibited depression/anxiety problems.32 Braga-Neto et al. evaluated 112 patients with SCA3 using a specific scale to characterize psychotic symptoms and brain SPECT analysis. Authors found psychotic symptoms in 5 patients and significant regional cerebral blood flow decrease in the cerebellum bilaterally and vermis in the SCA3 group, although no significant differences were found between patients with and without psychotic symptoms.33

The major strengths of this study include the systematic and objective assessment of neuropsychological features in a large sample of patients with SCA10. We believe that our data are relevant because they show that SCA10 patients present with visuospatial and executive dysfunction, consistent with the symptoms reported in the CCAS described by Schmahmann JD in 1998. However, our study should be interpreted in the context of some limitations. A main limitation is the brief battery of cognitive tests applied; future studies including more detailed and specific neuropsychological tests should be performed, as well as functional imaging studies in order to investigate the physiopathology of cognitive deficits in SCA10.

In conclusion, our study showed mild cognitive and mood dysfunctions in patients with SCA10 that may characterize the well-known CCAS. The description of these findings is an important clinical phenomenon that may guide physicians in specific disease management and improve quality of life of these patients.

Author contribution. Dr. Moro contributed to the study concept and design, acquisition of data, analysis and interpretation of data, drafting of the manuscript and critical revision of the manuscript. Dr. Teive contributed to drafting of the manuscript and critical revision of the manuscript for key intellectual content.


1. Teive HA. Spinocerebellar Degenerations in Japan. New insights from an epidemiological study. Neuroepidemiology. 2009;32(3):184-5.

2. Durr A. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. Lancet Neurology. 2010;9(9):885-94.

3. Schöls L, Bauer P, Schmidt T, Schulte T, Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 2004;3(5):291-304.

4. Klockgether T, Lüdtke R, Kramer B, Abele M, Bürk K, Schöls L, et al: The natural history of degenerative ataxia: a retrospective study of 466 patients. Brain. 1998;121(4):589-600.

5. Harding AE. The hereditary ataxias and related disorders. Edimburgh: Churchill Livingstone, 1984.

6. Teive HAG. Spinocerebellar Ataxias. Arq Neuropsiquiatr. 2009;67(4): 1133-42.

7. Braga-Neto P, Pedroso JL, Alessi H, Dutra LA, Felício AC, Minett T, et al. Cerebellar Cognitive Affective Syndrome in Machado Joseph Disease: Core Clinical Features. Cerebellum. 2012;11:549-56.

8. Manto M, Lorivel T. Cognitive repercussions of hereditary cerebellar disorders. Cortex 2011;47:81-100.

9. Bürk K, Globas C, Bösch S, Klockgether T, Zühlke C, Daum I, et al. Cognitive deficits in spinocerebellar ataxia type 1, 2 and 3. J Neurol. 2003;250:207-11.

10. O'Hearn E, Holmes SE, Calvert PC, Ross CA, Margolis RL. SCA12: Tremor with cerebelar and cortical atrophy is associated with a CAG repeat expansion. Neurology. 2001;56:299-303.

11. De Michele G, Maltecca F, Carella M, Volpe G, Orio M, De Falco A, et al. Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17. Neurol Sci. 2003;24:166-7.

12. Rolfs A, Koeppen AH, Bauer I, Bauer P, Buhlmann S, Topka H, et al. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). Ann Neurol. 2003;54:367-75.

13. Schelhaas HJ, van de Warrenburg BP, Hageman G, Ippel EE, van Hout M, Kremer B. Cognitive impairments in SCA19. Acta Neurol Belg. 2003;103:199-205.

14. Delplanque J, Devos D, Vuillaume I, De Becdelievre A, Vangelder E, Maurage CA, et al. Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21). Cerebellum. 2008;179-83.

15. Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet. 2008;26:191-4.

16. Raskin S, Ashizawa T, Teive HAG, Arruda WO, Fang P, Gao R, et al. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10. Arch Neurol. 2007;64:591-4.

17. Rasmunssen A, Matsuura T, Ruano L, Yescas P, Ochoa A, Ashizawa T, et al. Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10. Ann Neurol. 2001;50:234-9.

18. Teive HAG, Munhoz RP, Raskin S, Arruda WO, Paola L, Werneck LC, et al. Spinocerebellar ataxia type 10: frequency of epilepsy in a large sample of Brazilian patients. Mov Disord. 2010;25:2875-8.

19. Braga-Neto P, Godeiro-Junior C, Dutra LA, Pedroso JL, Barsottini OG. Translation and validation into Brazilian version of the Scale of the Assessment and Rating of Ataxia (SARA). Arq Neuropsiquiatr. 2010;68:228-30.

20. Gorenstein C, Andrade L, Vieira Filho AH, Tung TC, Artes R. Psychometric properties of the Portuguese version of the Beck Depression Inventory on Brazilian college students. J Clin Psychol. 1999;55:

21. Hamilton M. The assessment of anxiety states by rating. Br J Med Psychol. 1953;32:50-5.

22. Brucki SM, Nitrini R, Caramelli P, Bertolucci PH, Okamoto IH. Suggestions for utilization of the mini-mental state examination in Brazil. Arq Neuropsiquiatr. 2003;61:777-81.

23. Dubois B, Slachevsky A, Litvan I, Pillon B. The FAB. A frontal assessment battery at bedside. Neurology. 2000;55:1621-6.

24. Freedman M, Kaplan E, Delis D, Morris R. Clock Drawing: a neuropsychological analysis. New York: Oxford University Press; 1994.

25. Trikamji B, Singh P, Mishra S. Spinocerebellar ataxia-10 with paranoid schizophrenia. Ann Indian Acad Neurol. 2015;18:93-95.

26. Schmahmann JD, Sherman JC. The cerebellar cognitive affective syndrome. Brain 1998;121:561-79.

27. Grasby PM, Frith CD, Friston KJ, Bench C, Frackowiak RSJ, Dolan RJ. Functional mapping of brain areas implicated in auditory-verbal memory function. Brain. 1993;116:1-20.

28. Schlösser R, Hutchinson M, Joseffer S, Rusinek H, Saarimaki A, Stevenson J, et al. Functional magnetic resonance imaging of human brain activity in a verbal fluency task. J Neurol Neurosurg Psychiatric. 1998;64:492-8.

29. Bürk K, Globas C, Bösch S, Gräber S, Abele M, Brice A, et al. Cognitive deficits in spinocerebellar ataxia 2. Brain 1999;122:769-777.

30. Kawai Y, Suenaga M, Watanabe H, Ito M, Kato K, Kato T, et al. Prefrontal hypoperfusion and cognitive dysfunction correlates to spinocerebellar ataxia type 6. J Neurol Sci. 2008;271:68-74.

31. Cecchin CR, Pires AP, Rieder CR, Monte TL, Silveira I, Carvalho T, et al. Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives. Community Genet. 2007;10:19-26.

32. Schmitz-Hübsch T, Coudert M, Giunti P, et al. Self-rated health status in spinocerebellar ataxia - results from a European multicenter study. Mov Disord. 2010;5:587-95.

33. Braga-Neto P, Pedroso JL, Gadelha A, Laureano MR, de Souza Noto C, Garrido GJ, Barsottini OG. Psychosis in Machado-Joseph disease: clinical correlates, pathophysiological discussion, and functional brain imaging. Expanding the cerebelar cognitive affective syndrome. Cerebellum. 2016;15:483-90.

1. PhD, Movement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de Clínicas, Curitiba, PR, Brazil
2. PhD, Federal University of Paraná, Curitiba, PR, Brazil

Adriana Moro
Rua Teixeira Soares, 50
80240-440 Curitiba PR - Brazil
E-mail: moro_adriana@yahoo.com.br

Received September 10, 2016.
Accepted in final form November 12, 2016.
Disclosure: The authors report no conflicts of interest.

This study was conducted at the Movement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de Clínicas, Curitiba, PR, Brazil.
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