Show simple item record

Authordc.contributor.authorCiampi, E. 
Authordc.contributor.authorUribe San Martin, R. 
Authordc.contributor.authorVásquez, M. 
Authordc.contributor.authorRuiz-Tagle, A. 
Authordc.contributor.authorLabbe, T. 
Authordc.contributor.authorCruz, J. P. 
Authordc.contributor.authorLillo Zurita, Patricia 
Authordc.contributor.authorSlachevsky Chonchol, Andrea 
Authordc.contributor.authorReyes, D. 
Authordc.contributor.authorReyes, A. 
Authordc.contributor.authorCárcamo-Rodríguez, C. 
Admission datedc.date.accessioned2018-07-19T22:57:52Z
Available datedc.date.available2018-07-19T22:57:52Z
Publication datedc.date.issued2018
Cita de ítemdc.identifier.citationMultiple Sclerosis and Related Disorders, 20 (2018): 122–128es_ES
Identifierdc.identifier.other10.1016/j.msard.2018.01.013
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/150059
Abstractdc.description.abstractBackground: Cognitive impairment is a relevant contributor of the medical and social burden in Progressive MS. Social Cognition, the neurocognitive processes underlying social interaction, has been explored mainly in European and North American cohorts, influencing social aspects of quality of life (QOI) of early MS patients and families. Few studies have studied Social Cognition in Progressive MS and the literature on its neuroanatomical bases or brain atrophy measurements is still scarce. Objectives: To explore the relationship between Social Cognition performance and its correlations with traditional cognitive domains, brain atrophy and QOL in primary and secondary Progressive MS patients. Methods: Cross-sectional analysis including: mini-Social-Cognition-and-Emotional-Assessment (mini-SEA), neuropsychological battery, disability, depression, fatigue, QOL, and brain volume. Results: Forty-three MS patients, 23 primary and 20 secondary Progressive, 65% women, mean age and disease duration of 57.2 and 15.7 years, respectively, with high levels of disability (median EDSS 6.0) and a widespread impairment in traditional domains (mostly episodic verbal/visual and working memories) were assessed. The Mini-SEA score was correlated with executive functions (cognitive shifts Rho: 0.55; p = 0.001) analyzing the whole group, and with visual episodic memory (Rho: 0.58, p = 0.009) in the primary Progressive MS group. Mini-SEA score was also correlated with total normalized grey matter volume (Rho: 0.48; p = 0.004). Particularly, atrophy within bilateral cortical regions of orbitofrontal, insula and cerebellum, and right regions of fusiform gyrus and precuneus were significantly associated with higher Social Cognition impairment. In this cohort, QOL was not correlated with Social Cognition, but with EDSS, fatigue and depression. Conclusions: In Progressive MS, Social Cognition is directly correlated with traditional cognitive domains such as executive function and episodic memory. It is also associated with global grey matter atrophy and regional atrophy within associative visual and executive cortical areas, but no correlations with QOL were found in this cohort. These findings may contribute to the understanding of the pathological bases behind Social Cognition in Progressive MS.es_ES
Patrocinadordc.description.sponsorshipCONICYT-PIA-Anillo ACT1416 CONICYT/Associative Research Program/Basal Funds Grant for Centers of Excellence FB 0003 CONICYT/FONDECYT 1160940 1140423 CORFO Innova Chile 14PIE-26946 CONICYT/FONDAP/15150012es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevieres_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceMultiple Sclerosis and Related Disorderses_ES
Keywordsdc.subjectMultiple Sclerosises_ES
Keywordsdc.subjectSocial Cognitiones_ES
Keywordsdc.subjectMRIes_ES
Keywordsdc.subjectQuality of lifees_ES
Keywordsdc.subjectCognitive impairmentes_ES
Keywordsdc.subjectNeuropsychologyes_ES
Títulodc.titleRelationship between social cognition and traditional cognitive impairment in progressive multiple sclerosis and possible implicated neuroanatomical regionses_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadortjnes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile