Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome

ABSTRACT: Cockayne syndrome (CS) is an autosomal recessive disease associated with premature aging, progressive multiorgan degeneration, and nervous system abnormalities including cerebral and cerebellar atrophy, brain calcifications, and white matter abnormalities. Although several clinical descrip...

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Autores:
Bocanegra García, Orfa Yamile
Báez Buitrago, Sandra Jimena
Couto, Blas
Herrera Murcia, Eduar
Trujillo Orrego, Natalia
Madrigal Zapata, Lucia del Socorro
Cardona Londoño, Juan Felipe
Manes, Facundo
Ibañez Barassi, Agustín
Villegas Lanau, Carlos Andrés
Tipo de recurso:
Article of investigation
Fecha de publicación:
2013
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/33512
Acceso en línea:
https://hdl.handle.net/10495/33512
Palabra clave:
Cockayne Syndrome
Síndrome de Cockayne
Cognition
Cognición
Executive Function
Función Ejecutiva
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
title Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
spellingShingle Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
Cockayne Syndrome
Síndrome de Cockayne
Cognition
Cognición
Executive Function
Función Ejecutiva
title_short Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
title_full Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
title_fullStr Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
title_full_unstemmed Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
title_sort Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome
dc.creator.fl_str_mv Bocanegra García, Orfa Yamile
Báez Buitrago, Sandra Jimena
Couto, Blas
Herrera Murcia, Eduar
Trujillo Orrego, Natalia
Madrigal Zapata, Lucia del Socorro
Cardona Londoño, Juan Felipe
Manes, Facundo
Ibañez Barassi, Agustín
Villegas Lanau, Carlos Andrés
dc.contributor.author.none.fl_str_mv Bocanegra García, Orfa Yamile
Báez Buitrago, Sandra Jimena
Couto, Blas
Herrera Murcia, Eduar
Trujillo Orrego, Natalia
Madrigal Zapata, Lucia del Socorro
Cardona Londoño, Juan Felipe
Manes, Facundo
Ibañez Barassi, Agustín
Villegas Lanau, Carlos Andrés
dc.contributor.researchgroup.spa.fl_str_mv Grupo Neuropsicología y Conducta
Grupo de Neurociencias de Antioquia
dc.subject.decs.none.fl_str_mv Cockayne Syndrome
Síndrome de Cockayne
Cognition
Cognición
Executive Function
Función Ejecutiva
topic Cockayne Syndrome
Síndrome de Cockayne
Cognition
Cognición
Executive Function
Función Ejecutiva
description ABSTRACT: Cockayne syndrome (CS) is an autosomal recessive disease associated with premature aging, progressive multiorgan degeneration, and nervous system abnormalities including cerebral and cerebellar atrophy, brain calcifications, and white matter abnormalities. Although several clinical descriptions of CS patients have reported developmental delay and cognitive impairment with relative preservation of social skills, no previous studies have carried out a comprehensive neuropsychological and social cognition assessment. Furthermore, no previous research in individuals with CS has examined the relationship between brain atrophy and performance on neuropsychological and social cognition tests. This study describes the case of an atypical late-onset type III CS patient who exceeds the mean life expectancy of individuals with this pathology. The patient and a group of healthy controls underwent a comprehensive assessment that included multiple neuropsychological and social cognition (emotion recognition, theory of mind, and empathy) tasks. In addition, we compared the pattern of atrophy in the patient to controls and to its concordance with ERCC8 gene expression in a healthy brain. The results showed memory, language, and executive deficits that contrast with the relative preservation of social cognition skills. The cognitive profile of the patient was consistent with his pattern of global cerebral and cerebellar loss of gray matter volume (frontal structures, bilateral cerebellum, basal ganglia, temporal lobe, and occipito-temporal/occipito-parietal regions), which in turn was anatomically consistent with the ERCC8 gene expression level in a healthy donor’s brain. The study of exceptional cases, such as the one described here, is fundamental to elucidating the processes that affect the brain in premature aging diseases, and such studies provide an important source of information for understanding the problems associated with normal and pathological aging.
publishDate 2013
dc.date.issued.none.fl_str_mv 2013
dc.date.accessioned.none.fl_str_mv 2023-02-16T21:15:53Z
dc.date.available.none.fl_str_mv 2023-02-16T21:15:53Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/33512
identifier_str_mv 1663-4365
url https://hdl.handle.net/10495/33512
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Front. Aging. Neurosci.
dc.relation.citationendpage.spa.fl_str_mv 18
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 5
dc.relation.ispartofjournal.spa.fl_str_mv Frontiers in Aging Neuroscience
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dc.publisher.spa.fl_str_mv Frontiers Media
dc.publisher.place.spa.fl_str_mv Lausana, Suiza
institution Universidad de Antioquia
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spelling Bocanegra García, Orfa YamileBáez Buitrago, Sandra JimenaCouto, BlasHerrera Murcia, EduarTrujillo Orrego, NataliaMadrigal Zapata, Lucia del SocorroCardona Londoño, Juan FelipeManes, FacundoIbañez Barassi, AgustínVillegas Lanau, Carlos AndrésGrupo Neuropsicología y ConductaGrupo de Neurociencias de Antioquia2023-02-16T21:15:53Z2023-02-16T21:15:53Z20131663-4365https://hdl.handle.net/10495/33512ABSTRACT: Cockayne syndrome (CS) is an autosomal recessive disease associated with premature aging, progressive multiorgan degeneration, and nervous system abnormalities including cerebral and cerebellar atrophy, brain calcifications, and white matter abnormalities. Although several clinical descriptions of CS patients have reported developmental delay and cognitive impairment with relative preservation of social skills, no previous studies have carried out a comprehensive neuropsychological and social cognition assessment. Furthermore, no previous research in individuals with CS has examined the relationship between brain atrophy and performance on neuropsychological and social cognition tests. This study describes the case of an atypical late-onset type III CS patient who exceeds the mean life expectancy of individuals with this pathology. The patient and a group of healthy controls underwent a comprehensive assessment that included multiple neuropsychological and social cognition (emotion recognition, theory of mind, and empathy) tasks. In addition, we compared the pattern of atrophy in the patient to controls and to its concordance with ERCC8 gene expression in a healthy brain. The results showed memory, language, and executive deficits that contrast with the relative preservation of social cognition skills. The cognitive profile of the patient was consistent with his pattern of global cerebral and cerebellar loss of gray matter volume (frontal structures, bilateral cerebellum, basal ganglia, temporal lobe, and occipito-temporal/occipito-parietal regions), which in turn was anatomically consistent with the ERCC8 gene expression level in a healthy donor’s brain. The study of exceptional cases, such as the one described here, is fundamental to elucidating the processes that affect the brain in premature aging diseases, and such studies provide an important source of information for understanding the problems associated with normal and pathological aging.COL0007551COL001074418application/pdfengFrontiers MediaLausana, Suizahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne SyndromeArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a86http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleCockayne SyndromeSíndrome de CockayneCognitionCogniciónExecutive FunctionFunción EjecutivaFront. Aging. 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