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DOI: 10.1590/0004-282X20180077
Quality of life in individuals with spinocerebellar ataxia type 10: a preliminary study
Qualidade de vida em indivíduos com ataxia espinocerebelar tipo 10: estudo preliminar
ABSTRACT
Spinocerebellar ataxia type 10 (SCA10) is characterized by gait ataxia, dysarthria, nystagmus, epilepsy, reduced cognitive ability and depression, which lead to functional loss and behavioral changes. These signs gradually evolve and may interfere with the physical, emotional, and social aspects of quality of life (QoL).
Objective: To assess the self-perception of quality of life and its association with disease duration, severity of ataxia, balance and functional independence.
Methods: This study focused on the disease duration, ataxia severity (SARA), balance (Berg Balance Scale), functionality (FIM, Lawton IADL) and QoL (SF-36 v.2) of 15 individuals with SCA10.
Results: The population sample consisted of eight females and seven males, with a mean age of 43.8 (± 8.2) years, mean age of symptom onset of 33.1 (± 8.9) years and mean disease duration of 9.8 (± 11.2) years. The mean Berg Balance Scale score was 47.2 (± 12), mean SARA score (n = 14) 11.5 (± 7.3), mean Lawton IADL score 20.4 (± 1.8) and mean FIM score 120.3 (± 5.4). Individuals with SCA10 had a greater impairment of QoL in the “role-physical” domain (p = 0.04). The longer the disease duration (p = 0.02), risk of falling (p = 0.04), severity of ataxia (p = 0.00) and functional dependence in activities of daily living (p = 0.03) and instrumental activities of daily living (p = 0.00), the worse the QoL was in the “physical functioning” domain, with a decrease of 1.62 points for each year of disease duration.
Conclusion: In this sample, the greatest impairment of QoL in individuals with SCA10 was observed in “physical functioning” and “physical role”.
RESUMO
A Ataxia Espinocerebelar tipo 10 (SCA10) caracteriza-se pela ataxia da marcha, disartria, nistagmo, epilepsia, redução da capacidade cognitiva e depressão, causando perda funcional e alterações comportamentais. Esses sinais evoluem gradualmente e podem interferir nos aspectos físicos, emocionais e sociais da Qualidade de Vida (QV).
Objetivo: Avaliar a autopercepção da qualidade de vida e sua associação com a duração da doença, gravidade da ataxia, equilíbrio e independência funcional.
Método: O estudo enfoca a duração da doença, gravidade da ataxia (SARA), equilíbrio (EEB), funcionalidade (MIF, Lawton) e QV (SF-36 v.2) de 15 indivíduos com SCA10.
Resultados: A amostra foi composta por oito indivíduos do sexo feminino, com média de idade de 43,8 (± 8,2), de idade de início dos sintomas 33,1 (± 8,9) e de tempo de doença de 9,8 (± 11,2) anos. A média do escore na Berg foi 47,2 (± 12,0), no SARA (n = 14) foi de 11,5 (± 7,3), na escala de LAWTON 20,4 (± 1,8) e na MIF 120,3 (± 5,4) pontos. Os Indivíduos com SCA10 apresentaram maior prejuízo na QV no domínio “Aspectos Físicos” (p = 0,04). Quanto maior a duração da doença (p = 0,02), risco de queda (p = 0,04), gravidade da ataxia (p = 0,00) e maior dependência funcional para AVD (p = 0,03) e AIVD (p = 0,00), pior a QV no domínio “Capacidade Funcional” com decréscimo de 1,62 ponto para cada ano no tempo de doença.
Conclusão: Nesta amostra, o comprometimento da QV em indivíduos com SCA10 foi observado nos domínios “Capacidade Funcional” e “Aspectos Físicos”.
Publikationsverlauf
Eingereicht: 27. Februar 2018
Angenommen: 07. Mai 2018
Artikel online veröffentlicht:
23. August 2023
© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Schöls L, Bauer P, Schmidt T, Schulte T, Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 2004 May;3(5):291-304. https://doi.org/10.1016/S1474-4422(04)00737-9
- 2 Brazis PW, Biller J, Masdeu JC. Localization in clinical neurology. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2001.
- 3 Teive HA, Munhoz RP, Arruda WO, Raskin S, Werneck LC, Ashizawa T. Spinocerebellar ataxia type 10: a review. Parkinsonism Relat Disord. 2011 Nov;17(9):655-61. https://doi.org/10.1016/j.parkreldis.2011.04.001
- 4 Graves TD, Cha YH, Hahn AF, Barohn R, Salajegheh MK, Griggs RC et al. Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation. Brain. 2014 Apr;137(Pt 4):1009-18. https://doi.org/10.1093/brain/awu012
- 5 Castilhos RM, Furtado GV, Gheno TC, Schaeffer P, Russo A, Barsottini O et al. Spinocerebellar ataxias in Brazil;frequencies and modulating effects of related genes. Cerebellum. 2014 Feb;13(1):17-28. https://doi.org/10.1007/s12311-013-0510-y
- 6 Silva BF, Finard SA, Olchik MR. Therapy speech impact in quality of life in patients with Machado-Joseph disease. Rev CEFAC. 2016;18(4):992-1000. https://doi.org/10.1590/1982-0216201618418515
- 7 The WHOQOL Group. The World Health Organization quality of life assessment (WHOQOL): position paper from the World Health Organization. Soc Sci Med. 1995;41(10):1403-9. https://doi.org/10.1016/0277-9536(95)00112-K
- 8 Monteiro R, Braile DM, Brandau R, Jatene FB. Focus on quality of life. Rev Bras Cir Cardiovasc. 2010 Oct-Dec;25(4):568-74. https://doi.org/10.1590/S0102-76382010000400022
- 9 World Health Organization. Constitution of The World Health Organization. New York, NT: World Health Organization;1946 [accessed 2017 Dec 15]. Available fom:http://apps.who.int/gb/bd/PDF/bd47/EN/constitution-en.pdf?ua=1
- 10 World Health Organization. Division on Mental Health and Prevention of Substance abuse. WHHOQOL measuring quality of life. Geneva: World Health Organizaton; 1997[accessed on 2017 Dec 15]. Available from:http://www.who.int/mental_health/media/68.pdf
- 11 Ciconelli RM, Ferraz MB, Santos W, Meinão I, Quaresma MR. Tradução para a língua portuguesa e validação do questionário genérico de avaliação de qualidade de vida SF-36 (Brasil SF-36). Rev Bras Reumatol. 1999;39(3):143-50.
- 12 Riberto M, Miyazaki MH, Jucá SSH, Sakamoto H, Pinto PPN, Battistella LR. Validação da Versão Brasileira da Medida de Independência Funcional. ACTAFISIATR.2004;11(2):72-76. http://dx.doi.org/10.5935/0104-7795.20040003
- 13 Araújo F, Pais-Ribeiro J, Oliveira A, Pinto C, Martins T. Validação da escala de Lawton e Brody numa amostra de idosos não institucionalizados. In: Actas do 7º Congresso Nacional de Psicologia da Saúde. Lisboa: ISPA; 2008. p. 217-20.
- 14 Miyamoto ST, Lombardi Junior I, Berg KO, Ramos LR, Natour J. Brazilian version of the Berg balance scale. Braz J Med Biol Res. 2004 Sep;37(9):1411-21. https://doi.org/10.1590/S0100-879X2004000900017
- 15 Yabe I, Matsushima M, Soma H, Basri R, Sasaki H. Usefulness of the Scale for Assessment and Rating of Ataxia (SARA). J Neurol Sci. 2008;266(1-2):164-6. https://doi.org/10.1016/j.jns.2007.09.021
- 16 Dancey C, Reidy J. Estatística sem matemática para Psicologia: usando SPSS para Windows. 3nd. Porto Alegre: Artmed; 2006.
- 17 Filippin NT, Piccinini AM, Libera LBD. Caracterização do equilíbrio, risco de quedas e qualidade de vida em pessoas com doença de Machado-Joseph. Fisioterapia Brasil. 2016;(17):4-9.
- 18 Aizawa CY, Pedroso JL, Braga-Neto P, Callegari MR, Barsottini OG. Patients with autosomal dominant spinocerebellar ataxia have more risk of falls, important balance impairment, and decreased ability to function. Arq Neuropsiquiatr. 2013 Aug;71(8):508-11. https://doi.org/10.1590/0004-282X20130094
- 19 Sánchez-López CR, Perestelo-Pérez L, Escobar A, López-Bastida J, Serrano-Aguilar P. Health-related quality of life in patients with spinocerebellar ataxia. Neurologia. 2017 Apr;32(3):143-51. https://doi.org/10.1016/j.nrl.2015.09.002
- 20 Landeiro GMB, Pedrozo CCR, Gomes MJ, de Araújo Oliveira E. Revisão sistemática dos estudos sobre qualidade de vida indexados na base de dados SciELO. Cienc Saúde Coletiva. 2011;16(10):4257-66. https://dx.doi.org/10.1590/S1413-81232011001100031
- 21 Azevedo ALS, Silva RA, Tomasi E, Quevedo LA. Doenças crçnicas e qualidade de vida na atenção primária à saúde. Cad.Saúde Pública.2013;29(9):1774-1782. http://dx.doi.org/10.1590/0102-311X00134812
- 22 Teive HA, Munhoz RP, Arruda WO, Lopes-Cendes I, Raskin S, Werneck LC, et al. Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families. Clinics (São Paulo). 2012;67(5):443-9. https://doi.org/10.6061/clinics/2012(05)07
- 23 Tai G, Yiu EM, Corben LA, Delatycki MB. A longitudinal study of the Friedreich Ataxia Impact Scale. J Neurol Sci. 2015 May;352(1-2):53-7. https://doi.org/10.1016/j.jns.2015.03.024
- 24 Laguardia J, Campos MR, Travassos C, Najar AL, Anjos LA, Vasconcellos MM. Dados normativos brasileiros do questionário Short Form-36 versão 2. Rev Bras Epidemiol. 2013;16(4):889-97. https://doi.org/10.1590/S1415-790X2013000400009
- 25 Moreira RC, Zonta MB, Araújo AP, Israel VL, Teive HA. Quality of life in Parkinson's disease patients: progression markers of mild to moderate stages. Arq Neuropsiquiatr. 2017 Aug;75(8):497-502. https://doi.org/10.1590/0004-282x20170091
- 26 Ware J, Snow KK, Kosinski M, Gandek B. SF-36 Health survey: manual and interpretation guide. Boston: New England Medical Center; 1993 [accessed on 2017 Dec 15]. Available from: https://www.researchgate.net/publication/313050850_SF36_Health_Survey_Manual_Interpretation_Guide
- 27 Marqueze EC, Moreno CRC. Satisfação no trabalho: uma breve revisão. Rev Bras Saúde Ocupacional. 2005;30(112):69-79. https://doi.org/10.1590/S0303-76572005000200007
- 28 Moro A, Teive HA. Cognitive impairment in Spinocerebellar ataxia type 10. Dement Neuropsychol. 2016 Oct-Dec;10(4):310-4. https://doi.org/10.1590/s1980-5764-2016dn1004009
- 29 Amarante TR, Takeda SY, Teive HA, Zonta MB. Impact of disease duration on functional status of patients with spinocerebellar ataxia type 2. Arq Neuropsiquiatr. 2017 Nov;75(11):773-7. https://doi.org/10.1590/0004-282x20170146