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dc.rights.licenseopenen_US
dc.contributor.authorMIMENZA-ALVARADO, Alberto J.
dc.contributor.authorSUING-ORTEGA, Maria J.
dc.contributor.authorTUSIE-LUNA, Teresa
dc.contributor.authorJUAREZ-CEDILLO, Teresa
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorAVILA-FUNES, Jose Alberto
dc.contributor.authorAGUILAR-NAVARRO, Sara G.
dc.date.accessioned2022-05-11T13:24:07Z
dc.date.available2022-05-11T13:24:07Z
dc.date.issued2022
dc.identifier.issn0034-8376en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/140038
dc.description.abstractEnBACKGROUND: The pathogenesis of mild cognitive impairment (MCI) is multifactorial and includes the presence of genetic variants such as the ε(4) allele of the apolipoprotein E gene (APOE-ε(4)). Association between the APOE-ε(4) carrier status and deleterious structural and functional changes on magnetic resonance imaging (MRI) has been previously described in individuals with Alzheimer's disease. However, the central nervous system changes may possibly develop in earlier stages of cognitive impairment, as reflected in MCI. OBJECTIVE: The objective of the study was to determine the association between APOE-ε(4) carrier status and qualitative changes on MRI (medial temporal and parietal atrophy), as well as the detection of white matter hyperintensities (WMH) in older adults with MCI, in the memory clinic of a tertiary care hospital in Mexico City. METHODS: A cross-sectional study of 72 adults aged 60 years or above who underwent an exhaustive clinical, neuroimaging, and neuropsychological evaluation. Multivariate logistic regression models were constructed to determine the association between APOE-ε(4) carrier status and qualitative/quantitative changes on MRI. RESULTS: Mean age was 75.2 years (± 7.2) and 64% were female. Twenty-one participants were cognitively normal and 51 had MCI. Almost 56% were APOE-ε(4) carriers and were associated with medial-temporal atrophy according to the Scheltens scale (odds ratio [OR]: 20.0, 95% confidence intervals [CI]: 3.03-131.7), parietal atrophy according to the Koedam's score (OR: 6.3; 95% CI 1.03-39.53), and WMH according to the Fazekas scale (OR: 11.7, 95% CI: 1.26-108.2), even after adjusting for age, educational level, and cardiovascular risk factors. CONCLUSION: The APOE-ε(4) carrier status was associated with medial temporal and parietal atrophy, as well as WMH. Our findings support the hypothesis suggesting the contribution of this genotype to neurodegeneration and cerebral vascular pathology.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subject.enMild cognitive impairment
dc.subject.enAPOE-ε4 carrier status
dc.subject.enMagnetic resonance imaging
dc.subject.enMexican mestizo older adults
dc.title.enAssociation between APOE-ε(4) Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
dc.typeArticle de revueen_US
dc.identifier.doi10.24875/ric.21000550en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed35354197en_US
bordeaux.journalRevista de Investigacion Clinicaen_US
bordeaux.page113-120en_US
bordeaux.volume74en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamACTIVE_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03665177
hal.version1
hal.date.transferred2022-05-11T13:24:09Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Revista%20de%20Investigacion%20Clinica&rft.date=2022&rft.volume=74&rft.issue=2&rft.spage=113-120&rft.epage=113-120&rft.eissn=0034-8376&rft.issn=0034-8376&rft.au=MIMENZA-ALVARADO,%20Alberto%20J.&SUING-ORTEGA,%20Maria%20J.&TUSIE-LUNA,%20Teresa&JUAREZ-CEDILLO,%20Teresa&AVILA-FUNES,%20Jose%20Alberto&rft.genre=article


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