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dc.rights.licenseopenen_US
dc.contributor.authorYORO-ZOHOUN, Ines
dc.contributor.authorHOUINATO, Dismand
dc.contributor.authorNUBUKPO, Philippe
dc.contributor.authorMBELESSO, Pascal
dc.contributor.authorNDAMBA-BANDZOUZI, Bebene
dc.contributor.authorLAMBERT, Jean-Charles
dc.contributor.authorCLEMENT, Jean-Pierre
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDARTIGUES, Jean-Francois
ORCID: 0000-0001-9482-5529
IDREF: 058586105
dc.contributor.authorPREUX, Pierre-Marie
dc.contributor.authorGUERCHET, Maelenn
dc.date.accessioned2021-05-11T09:06:05Z
dc.date.available2021-05-11T09:06:05Z
dc.date.issued2021-03-15
dc.identifier.issn1741-203X (Electronic) 1041-6102 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/72137
dc.description.abstractEnOBJECTIVES: To evaluate the association between neuropsychiatric symptoms and apolipoprotein E (APOE) ϵ4 allele among older people in Central African Republic (CAR) and the Republic of Congo (ROC). DESIGN: Multicenter population-based study following a two-phase design. SETTING: From 2011 to 2012, rural and urban areas of CAR and ROC. PARTICIPANTS: People aged 65 and over. MEASUREMENTS: Following screening using the Community Screening Interview for Dementia, participants with low cognitive scores (CSI-D ≤ 24.5) underwent clinical assessment. Dementia diagnosis followed the DSM-IV criteria and Peterson's criteria were considered for Mild Cognitive Impairment (MCI). Neuropsychiatric symptoms were evaluated through the brief version of the Neuropsychiatric Inventory (NPI-Q). Blood samples were taken from all consenting participants before APOE genotyping was performed by polymerase chain reaction (PCR). Logistic regression models were used to evaluate the association between the APOE ϵ4 allele and neuropsychiatric symptoms. RESULTS: Overall, 322 participants had complete information on both neuropsychiatric symptoms and APOE status. Median age was 75.0 years and 81.1% were female. Neuropsychiatric symptoms were reported by 192 participants (59.8%) and at least 1 APOE ϵ4 allele was present in 135 (41.9%). APOE ϵ4 allele was not significantly associated with neuropsychiatric symptoms but showed a trend toward a protective effect in some models. CONCLUSION: This study is the first one investigating the association between APOE ϵ4 and neuropsychiatric symptoms among older people in sub-Saharan Africa (SSA). Preliminary findings indicate that the APOE ϵ4 allele was not associated with neuropsychiatric symptoms. Further research seems, however, needed to investigate the protective trend found in this study.
dc.language.isoENen_US
dc.subject.enNeuropsychiatric symptoms
dc.subject.enApolipoprotein E
dc.subject.enϵ4 allele
dc.subject.enDementia
dc.subject.enCognitive disorders
dc.subject.enSub-Saharan Africa
dc.title.enApolipoprotein E ϵ4 allele and neuropsychiatric symptoms among older adults in Central Africa (EPIDEMCA study)
dc.typeArticle de revueen_US
dc.identifier.doi10.1017/S1041610220003993en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed33715647en_US
bordeaux.journalInternational Psychogeriatricsen_US
bordeaux.page295-306en_US
bordeaux.volume33en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamSEPIAen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
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