Factors that indicate performance on the MoCA 7.3 in healthy adults over 50 years old

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psicoloxía Evolutiva e da Educación
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicina
dc.contributor.authorBugallo Carrera, César
dc.contributor.authorDosil Díaz, Carlos
dc.contributor.authorPereiro Rozas, Arturo X.
dc.contributor.authorAnido Rifón, Luis
dc.contributor.authorGandoy Crego, Manuel
dc.date.accessioned2025-03-18T10:03:38Z
dc.date.available2025-03-18T10:03:38Z
dc.date.issued2024-06-01
dc.description.abstractHuman aging is a physiological, progressive, heterogeneous global process that causes a decline of all body systems, functions, and organs. Throughout this process, cognitive function suffers an incremental decline with broad interindividual variability. The first objective of this study was to examine the differences in the performance on the MoCA test (v. 7.3) per gender and the relationship between the performance and the variables age, years of schooling, and depressive symptoms .The second objective was to identify factors that may influence the global performance on the MoCA test (v. 7.3) and of the domains orientation, language, memory, attention/calculation, visuospatial and executive function, abstraction, and identification. A cross-sectional study was carried out in which five hundred seventy-three (573) cognitively healthy adults ≥ 50 years old were included in the study. A sociodemographic questionnaire, the GDS-15 questionnaire to assess depression symptoms and the Spanish version of the MoCA Test (v 7.3) were administered. The evaluations were carried out between the months of January and June 2022. Differences in the MoCA test performance per gender was assessed with Student’s t-test for independent samples. The bivariate Pearson correlation was applied to examine the relationship between total scoring of the MoCA test performance and the variables age, years of schooling, and depressive symptoms. Different linear multiple regression analyses were performed to determine variables that could influence the MoCA test performance. We found gender-related MoCA Test performance differences. An association between age, years of schooling, and severity of depressive symptoms was observed. Age, years of schooling, and severity of depressive symptoms influence the MoCA Test performance, while gender does not
dc.description.peerreviewedSI
dc.identifier.citationBugallo-Carrera, C., Dosil-Díaz, C., Pereiro, A.X. et al. Factors that indicate performance on the MoCA 7.3 in healthy adults over 50 years old. BMC Geriatr 24, 482 (2024). https://doi.org/10.1186/s12877-024-05102-1
dc.identifier.doi10.1186/s12877-024-05102-1
dc.identifier.issn1471-2318
dc.identifier.urihttps://hdl.handle.net/10347/40292
dc.issue.number482
dc.journal.titleBMC Geriatrics
dc.language.isoeng
dc.page.final7
dc.page.initial1
dc.publisherSpringer Nature
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115137RB-I00
dc.relation.publisherversionhttps://doi.org/10.1186/s12877-024-05102-1
dc.rights© The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAging
dc.subjectMoCA Test performance
dc.subjectCognitive reserve
dc.subjectDepressive symptoms
dc.subjectMoCA test
dc.subject.classification32 Ciencias médicas
dc.titleFactors that indicate performance on the MoCA 7.3 in healthy adults over 50 years old
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number24
dspace.entity.typePublication
relation.isAuthorOfPublication37113dae-6dfb-4f62-8497-baa133675e7f
relation.isAuthorOfPublicationf2656e67-d20a-45e3-b84e-c4361d7d7a43
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relation.isAuthorOfPublication33a7995a-bcf5-4d25-9ac6-1a20565bc1ab
relation.isAuthorOfPublication.latestForDiscovery37113dae-6dfb-4f62-8497-baa133675e7f

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