Mostrar el registro sencillo del ítem

dc.contributor.author
Slachevsky, Andrea  
dc.contributor.author
Forno, Gonzalo  
dc.contributor.author
Barraza, Paulo  
dc.contributor.author
Mioshi, Eneida  
dc.contributor.author
Delgado, Carolina  
dc.contributor.author
Lillo, Patricia  
dc.contributor.author
Henriquez, Fernando  
dc.contributor.author
Bravo, Eduardo  
dc.contributor.author
Farias, Mauricio  
dc.contributor.author
Muñoz Neira, Carlos  
dc.contributor.author
Ibañez, Agustin Mariano  
dc.contributor.author
Parra, Mario A.  
dc.contributor.author
Hornberger, Michael  
dc.date.available
2021-07-13T17:40:07Z  
dc.date.issued
2019-06  
dc.identifier.citation
Slachevsky, Andrea; Forno, Gonzalo; Barraza, Paulo; Mioshi, Eneida; Delgado, Carolina; et al.; Mapping the neuroanatomy of functional decline in Alzheimer’s disease from basic to advanced activities of daily living; Dr. Dietrich Steinkopff Verlag; Journal of Neurology; 266; 6; 6-2019; 1310-1322  
dc.identifier.issn
0340-5354  
dc.identifier.uri
http://hdl.handle.net/11336/136001  
dc.description.abstract
Background: Impairments in activities of daily living (ADL) are a criterion for Alzheimer’s disease (AD) dementia. However, ADL gradually decline in AD, impacting on advanced (a-ADL, complex interpersonal or social functioning), instrumental (IADL, maintaining life in community), and finally basic functions (BADL, activities related to physiological and self-maintenance needs). Information and communication technologies (ICT) have become an increasingly important aspect of daily functioning. Yet, the links of ADL, ICT, and neuropathology of AD dementia are poorly understood. Such knowledge is critical as it can provide biomarker evidence of functional decline in AD. Methods: ADL were evaluated with the Technology–Activities of Daily Living Questionnaire (T-ADLQ) in 33 patients with AD and 30 controls. ADL were divided in BADL, IADL, and a-ADL. The three domain subscores were covaried against gray matter atrophy via voxel-based morphometry. Results: Our results showed that three domain subscores of ADL correlate with several brain structures, with a varying degree of overlap between them. BADL score correlated mostly with frontal atrophy, IADL with more widespread frontal, temporal and occipital atrophy and a-ADL with occipital and temporal atrophy. Finally, ICT subscale was associated with atrophy in the precuneus. Conclusions: The association between ADL domains and neurodegeneration in AD follows a traceable neuropathological pathway which involves different neural networks. This the first evidence of ADL phenotypes in AD characterised by specific patterns of functional decline and well-defined neuropathological changes. The identification of such phenotypes can yield functional biomarkers for dementias such as AD.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Dr. Dietrich Steinkopff Verlag  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
ACTIVITIES OF DAILY LIVING  
dc.subject
ALZHEIMER’S DISEASE  
dc.subject
FUNCTIONAL IMPAIRMENT  
dc.subject
TECHNOLOGY–ACTIVITIES OF DAILY LIVING QUESTIONNAIRE  
dc.subject.classification
Neurociencias  
dc.subject.classification
Medicina Básica  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Mapping the neuroanatomy of functional decline in Alzheimer’s disease from basic to advanced activities of daily living  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-11-20T17:29:17Z  
dc.journal.volume
266  
dc.journal.number
6  
dc.journal.pagination
1310-1322  
dc.journal.pais
Alemania  
dc.journal.ciudad
Heidelberg  
dc.description.fil
Fil: Slachevsky, Andrea. Universidad de Chile; Chile. Clínica Alemana-Universidad del Desarrollo. Departamento de Medicina. Servicio de Neurología; Chile  
dc.description.fil
Fil: Forno, Gonzalo. Universidad de Chile; Chile  
dc.description.fil
Fil: Barraza, Paulo. Universidad de Chile; Chile  
dc.description.fil
Fil: Mioshi, Eneida. University of East Anglia; Reino Unido  
dc.description.fil
Fil: Delgado, Carolina. Universidad de Chile; Chile  
dc.description.fil
Fil: Lillo, Patricia. Universidad de Chile; Chile  
dc.description.fil
Fil: Henriquez, Fernando. Universidad de Chile; Chile  
dc.description.fil
Fil: Bravo, Eduardo. Institute of Neurosurgery Asenjo; Chile  
dc.description.fil
Fil: Farias, Mauricio. Institute of Neurosurgery Asenjo; Chile  
dc.description.fil
Fil: Muñoz Neira, Carlos. Universidad de Chile; Chile  
dc.description.fil
Fil: Ibañez, Agustin Mariano. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Favaloro; Argentina. Universidad Autónoma del Caribe; Colombia. Universidad Adolfo Ibáñez; Chile. Australian Research Council (acr); Australia  
dc.description.fil
Fil: Parra, Mario A.. Universidad Autónoma del Caribe; Colombia. University of Strathclyde; Reino Unido  
dc.description.fil
Fil: Hornberger, Michael. University of East Anglia; Reino Unido. Norfolk and Suffolk Foundation Trust; Reino Unido  
dc.journal.title
Journal of Neurology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s00415-019-09260-w  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs00415-019-09260-w