Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale
Previous to appearance of motor alterations in Huntington's disease (HD), there can be a discreet cognitive deterioration. During the first decade of evolution of the disease, Mini-Mental State Examination and IQ test may be normal and application of highly sensitive tests become necessary in p...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2008
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22866
- Acceso en línea:
- https://repository.urosario.edu.co/handle/10336/22866
- Palabra clave:
- Adult
Article
Cognitive defect
Controlled study
Human
Huntington chorea
Intelligence quotient
Intelligence test
Major clinical study
Mental deterioration
Rating scale
Reading
Word recognition
Cognition
Huntington's disease
Stroop interference test
- Rights
- License
- Abierto (Texto Completo)
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787982d6-9ba5-408a-ab39-a88dd90da5e8-138dc5780-27b9-4de7-82cf-f8d3ec331c10-1a78a0f32-c7a6-4181-9d81-de7ded2d2087-1f45ab769-682d-4523-84b5-108a5cfae3db-12020-05-25T23:58:27Z2020-05-25T23:58:27Z2008Previous to appearance of motor alterations in Huntington's disease (HD), there can be a discreet cognitive deterioration. During the first decade of evolution of the disease, Mini-Mental State Examination and IQ test may be normal and application of highly sensitive tests become necessary in prediction of anomalies. The cognitive deterioration of HD subjects with less than 10 years evolution was studied using the tests of Verbal Fluency, Symbol Digit Modalities and the entire 3 parts of the Stroop test. A transversal analysis in 61 subjects was employed to seek for correlations of results in these tests and time of evolution of disease and motor deterioration. In the 52 subjects that finished every subsequent evaluation, rates of six-month, yearly and eighteen-month change were estimated. All cognitive tests were significantly related to the motor subscale and time of evolution. Correlation of results in the Stroop test with motor scale produced a Pearson's correlation coefficient of -0.76 for word reading (part A), -0.68 for color naming (B) and -0.64 for interference test (C). Time of evolution was more highly related to the 2 remaining tests. The longitudinal study did not set in evidence any significant change with the exception of the quick reading section of Stroop A test, which showed 7 points deterioration in 18 months. This test turned out to be more sensitive than the other complex tasks for detection of any deterioration. ©INNN, 2008.application/pdf10285938https://repository.urosario.edu.co/handle/10336/22866eng30No. 125Archivos de NeurocienciasVol. 13Archivos de Neurociencias, ISSN:10285938, Vol.13, No.1 (2008); pp. 25-30https://www.scopus.com/inward/record.uri?eid=2-s2.0-45549098678&partnerID=40&md5=eae0903ba01ee2a139f5278921be6b65Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAdultArticleCognitive defectControlled studyHumanHuntington choreaIntelligence quotientIntelligence testMajor clinical studyMental deteriorationRating scaleReadingWord recognitionCognitionHuntington's diseaseStroop interference testAnalysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scaleAnálisis del deterioro cognoscitivo en pacientes con enfermedad de Huntington mediante las pruebas de la escala unificada (UHDRS)articleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Boll M.-C.Martínez E.M.B.Ochoa A.Alonso Ma.E.ORIGINALane081e.pdfapplication/pdf96902https://repository.urosario.edu.co/bitstreams/064db637-d41c-4b77-bbca-6c1772a15d82/downloadd0c43313b76f91ff780052b776ce74a6MD51TEXTane081e.pdf.txtane081e.pdf.txtExtracted texttext/plain26590https://repository.urosario.edu.co/bitstreams/c9c5c2ab-5e21-41d3-a9f6-ba716e9eae90/downloadb2819e5c403d0d12d0a34e13f90fb9daMD52THUMBNAILane081e.pdf.jpgane081e.pdf.jpgGenerated Thumbnailimage/jpeg4476https://repository.urosario.edu.co/bitstreams/e641aada-862f-4b83-84b6-7a532755bab3/downloadde8cdc5d0d55502e06e662350acd1fe6MD5310336/22866oai:repository.urosario.edu.co:10336/228662022-05-02 07:37:14.40031https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
dc.title.TranslatedTitle.spa.fl_str_mv |
Análisis del deterioro cognoscitivo en pacientes con enfermedad de Huntington mediante las pruebas de la escala unificada (UHDRS) |
title |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
spellingShingle |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale Adult Article Cognitive defect Controlled study Human Huntington chorea Intelligence quotient Intelligence test Major clinical study Mental deterioration Rating scale Reading Word recognition Cognition Huntington's disease Stroop interference test |
title_short |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
title_full |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
title_fullStr |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
title_full_unstemmed |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
title_sort |
Analysis of cognitive decline in patients with Huntington's disease using unified Huntington's disease rating scale |
dc.subject.keyword.spa.fl_str_mv |
Adult Article Cognitive defect Controlled study Human Huntington chorea Intelligence quotient Intelligence test Major clinical study Mental deterioration Rating scale Reading Word recognition Cognition Huntington's disease Stroop interference test |
topic |
Adult Article Cognitive defect Controlled study Human Huntington chorea Intelligence quotient Intelligence test Major clinical study Mental deterioration Rating scale Reading Word recognition Cognition Huntington's disease Stroop interference test |
description |
Previous to appearance of motor alterations in Huntington's disease (HD), there can be a discreet cognitive deterioration. During the first decade of evolution of the disease, Mini-Mental State Examination and IQ test may be normal and application of highly sensitive tests become necessary in prediction of anomalies. The cognitive deterioration of HD subjects with less than 10 years evolution was studied using the tests of Verbal Fluency, Symbol Digit Modalities and the entire 3 parts of the Stroop test. A transversal analysis in 61 subjects was employed to seek for correlations of results in these tests and time of evolution of disease and motor deterioration. In the 52 subjects that finished every subsequent evaluation, rates of six-month, yearly and eighteen-month change were estimated. All cognitive tests were significantly related to the motor subscale and time of evolution. Correlation of results in the Stroop test with motor scale produced a Pearson's correlation coefficient of -0.76 for word reading (part A), -0.68 for color naming (B) and -0.64 for interference test (C). Time of evolution was more highly related to the 2 remaining tests. The longitudinal study did not set in evidence any significant change with the exception of the quick reading section of Stroop A test, which showed 7 points deterioration in 18 months. This test turned out to be more sensitive than the other complex tasks for detection of any deterioration. ©INNN, 2008. |
publishDate |
2008 |
dc.date.created.spa.fl_str_mv |
2008 |
dc.date.accessioned.none.fl_str_mv |
2020-05-25T23:58:27Z |
dc.date.available.none.fl_str_mv |
2020-05-25T23:58:27Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.issn.none.fl_str_mv |
10285938 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/22866 |
identifier_str_mv |
10285938 |
url |
https://repository.urosario.edu.co/handle/10336/22866 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
30 |
dc.relation.citationIssue.none.fl_str_mv |
No. 1 |
dc.relation.citationStartPage.none.fl_str_mv |
25 |
dc.relation.citationTitle.none.fl_str_mv |
Archivos de Neurociencias |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 13 |
dc.relation.ispartof.spa.fl_str_mv |
Archivos de Neurociencias, ISSN:10285938, Vol.13, No.1 (2008); pp. 25-30 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-45549098678&partnerID=40&md5=eae0903ba01ee2a139f5278921be6b65 |
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http://purl.org/coar/access_right/c_abf2 |
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Abierto (Texto Completo) |
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Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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