Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients

Detalhes bibliográficos
Autor(a) principal: Stella, Florindo [UNESP]
Data de Publicação: 2016
Outros Autores: Laks, Jerson, Govone, José Sílvio [UNESP], De Medeiros, Kate, Forlenza, Orestes Vicente
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1017/S1041610215002069
http://hdl.handle.net/11449/172328
Resumo: Background: Data on the relationship between behavioral disturbances in Alzheimer's disease (AD) and global clinical deterioration is still controversial. The purpose of this study was to explore potential correlations of neuropsychiatric syndromes with global clinical deterioration in patients with AD, with particular consideration on severity levels of dementia. Methods: AD patients (n = 156) aged 76.7 years from Brazilian clinical centers were assessed to diagnose the five neuropsychiatric syndromes measured by the Neuropsychiatric Inventory-Clinician rating scale (NPI-C): psychosis, agitation, affective, apathy, and sleep. These syndromes were then analyzed for their correlation with the Global Deterioration Scale (GDS). To analyze the association of neuropsychiatric syndromes with the GDS, considering the total sample and patients grouped by dementia severity levels, we applied the coefficient of multiple correlation (Ryy), adjusted multiple linear regression, and the coefficient of determination (R2yx). We tested the significance of correlation coefficients using the Student t-test for simple correlations (a single independent variable) and analysis of variance (ANOVA) for multiple correlations. ANOVA was also used to compare means of demographic and some clinical variables at different levels of dementia. Results: For the total sample, apathy and agitation syndromes were most strongly correlated (0.74; 0.72, respectively) with clinical deterioration according to the GDS, followed by psychosis (0.59), affective (0.45), and sleep syndromes (0.34). Agitation significantly correlated with mild and moderate dementia (CDR 1: 0.45; and CDR 2: 0.69, respectively). At CDR 2, agitation and affective syndromes were most strongly correlated (0.69; 0.59, respectively) with clinical deterioration while at CDR 3, the apathy syndrome was most strongly correlated with clinical deterioration (0.52). Conclusions: Agitation, apathy, and affective disorders were the syndromes most strongly correlated with global deterioration in AD patients, becoming more evident at severe stages of dementia.
id UNSP_ea8ed4636c5103331debd3cd371a36b1
oai_identifier_str oai:repositorio.unesp.br:11449/172328
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patientsAlzheimer's diseasedementiaglobal deteriorationneuropsychiatric syndromesBackground: Data on the relationship between behavioral disturbances in Alzheimer's disease (AD) and global clinical deterioration is still controversial. The purpose of this study was to explore potential correlations of neuropsychiatric syndromes with global clinical deterioration in patients with AD, with particular consideration on severity levels of dementia. Methods: AD patients (n = 156) aged 76.7 years from Brazilian clinical centers were assessed to diagnose the five neuropsychiatric syndromes measured by the Neuropsychiatric Inventory-Clinician rating scale (NPI-C): psychosis, agitation, affective, apathy, and sleep. These syndromes were then analyzed for their correlation with the Global Deterioration Scale (GDS). To analyze the association of neuropsychiatric syndromes with the GDS, considering the total sample and patients grouped by dementia severity levels, we applied the coefficient of multiple correlation (Ryy), adjusted multiple linear regression, and the coefficient of determination (R2yx). We tested the significance of correlation coefficients using the Student t-test for simple correlations (a single independent variable) and analysis of variance (ANOVA) for multiple correlations. ANOVA was also used to compare means of demographic and some clinical variables at different levels of dementia. Results: For the total sample, apathy and agitation syndromes were most strongly correlated (0.74; 0.72, respectively) with clinical deterioration according to the GDS, followed by psychosis (0.59), affective (0.45), and sleep syndromes (0.34). Agitation significantly correlated with mild and moderate dementia (CDR 1: 0.45; and CDR 2: 0.69, respectively). At CDR 2, agitation and affective syndromes were most strongly correlated (0.69; 0.59, respectively) with clinical deterioration while at CDR 3, the apathy syndrome was most strongly correlated with clinical deterioration (0.52). Conclusions: Agitation, apathy, and affective disorders were the syndromes most strongly correlated with global deterioration in AD patients, becoming more evident at severe stages of dementia.Biosciences Institute Campus of Rio Claro-SP UNESP - Universidade Estadual PaulistaDepartment and Institute of Psychiatry Faculty of Medicine University of Sao PauloCenter for Alzheimer's Disease and Related Disorders Institute of Psychiatry Federal University of Rio de Janeiro-RJDepartment of Statistics Applied Mathematics and Computer Sciences UNESP - Universidade Estadual Paulista Center of Environmental Studies (CEA)Department of Sociology and Gerontology Miami UniversityBiosciences Institute Campus of Rio Claro-SP UNESP - Universidade Estadual PaulistaDepartment of Statistics Applied Mathematics and Computer Sciences UNESP - Universidade Estadual Paulista Center of Environmental Studies (CEA)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Federal University of Rio de Janeiro-RJMiami UniversityStella, Florindo [UNESP]Laks, JersonGovone, José Sílvio [UNESP]De Medeiros, KateForlenza, Orestes Vicente2018-12-11T16:59:44Z2018-12-11T16:59:44Z2016-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article779-786application/pdfhttp://dx.doi.org/10.1017/S1041610215002069International Psychogeriatrics, v. 28, n. 5, p. 779-786, 2016.1741-203X1041-6102http://hdl.handle.net/11449/17232810.1017/S10416102150020692-s2.0-849502988392-s2.0-84950298839.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Psychogeriatrics1,048info:eu-repo/semantics/openAccess2024-04-10T19:22:25Zoai:repositorio.unesp.br:11449/172328Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-04-10T19:22:25Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
title Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
spellingShingle Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
Stella, Florindo [UNESP]
Alzheimer's disease
dementia
global deterioration
neuropsychiatric syndromes
title_short Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
title_full Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
title_fullStr Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
title_full_unstemmed Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
title_sort Association of neuropsychiatric syndromes with global clinical deterioration in Alzheimer's disease patients
author Stella, Florindo [UNESP]
author_facet Stella, Florindo [UNESP]
Laks, Jerson
Govone, José Sílvio [UNESP]
De Medeiros, Kate
Forlenza, Orestes Vicente
author_role author
author2 Laks, Jerson
Govone, José Sílvio [UNESP]
De Medeiros, Kate
Forlenza, Orestes Vicente
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Federal University of Rio de Janeiro-RJ
Miami University
dc.contributor.author.fl_str_mv Stella, Florindo [UNESP]
Laks, Jerson
Govone, José Sílvio [UNESP]
De Medeiros, Kate
Forlenza, Orestes Vicente
dc.subject.por.fl_str_mv Alzheimer's disease
dementia
global deterioration
neuropsychiatric syndromes
topic Alzheimer's disease
dementia
global deterioration
neuropsychiatric syndromes
description Background: Data on the relationship between behavioral disturbances in Alzheimer's disease (AD) and global clinical deterioration is still controversial. The purpose of this study was to explore potential correlations of neuropsychiatric syndromes with global clinical deterioration in patients with AD, with particular consideration on severity levels of dementia. Methods: AD patients (n = 156) aged 76.7 years from Brazilian clinical centers were assessed to diagnose the five neuropsychiatric syndromes measured by the Neuropsychiatric Inventory-Clinician rating scale (NPI-C): psychosis, agitation, affective, apathy, and sleep. These syndromes were then analyzed for their correlation with the Global Deterioration Scale (GDS). To analyze the association of neuropsychiatric syndromes with the GDS, considering the total sample and patients grouped by dementia severity levels, we applied the coefficient of multiple correlation (Ryy), adjusted multiple linear regression, and the coefficient of determination (R2yx). We tested the significance of correlation coefficients using the Student t-test for simple correlations (a single independent variable) and analysis of variance (ANOVA) for multiple correlations. ANOVA was also used to compare means of demographic and some clinical variables at different levels of dementia. Results: For the total sample, apathy and agitation syndromes were most strongly correlated (0.74; 0.72, respectively) with clinical deterioration according to the GDS, followed by psychosis (0.59), affective (0.45), and sleep syndromes (0.34). Agitation significantly correlated with mild and moderate dementia (CDR 1: 0.45; and CDR 2: 0.69, respectively). At CDR 2, agitation and affective syndromes were most strongly correlated (0.69; 0.59, respectively) with clinical deterioration while at CDR 3, the apathy syndrome was most strongly correlated with clinical deterioration (0.52). Conclusions: Agitation, apathy, and affective disorders were the syndromes most strongly correlated with global deterioration in AD patients, becoming more evident at severe stages of dementia.
publishDate 2016
dc.date.none.fl_str_mv 2016-05-01
2018-12-11T16:59:44Z
2018-12-11T16:59:44Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1017/S1041610215002069
International Psychogeriatrics, v. 28, n. 5, p. 779-786, 2016.
1741-203X
1041-6102
http://hdl.handle.net/11449/172328
10.1017/S1041610215002069
2-s2.0-84950298839
2-s2.0-84950298839.pdf
url http://dx.doi.org/10.1017/S1041610215002069
http://hdl.handle.net/11449/172328
identifier_str_mv International Psychogeriatrics, v. 28, n. 5, p. 779-786, 2016.
1741-203X
1041-6102
10.1017/S1041610215002069
2-s2.0-84950298839
2-s2.0-84950298839.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Psychogeriatrics
1,048
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 779-786
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1803046666691936256