<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.inpsyc.2025.100129</dc:identifier><dc:language>eng</dc:language><dc:creator>Molina-Torres, Nora</dc:creator><dc:creator>Platero, Carlos</dc:creator><dc:creator>Pérez-Berasategui, Oscar</dc:creator><dc:creator>Andrés-Benito, Pol</dc:creator><dc:creator>Povedano, Mónica</dc:creator><dc:creator>Mesa-Lampré, Pilar</dc:creator><dc:creator>Abadía-Morales, María</dc:creator><dc:creator>Calvo, Ana-Cristina</dc:creator><dc:creator>Lobo, Antonio</dc:creator><dc:creator>De La Cámara-Izquierdo, Concepción</dc:creator><dc:creator>Osta, Rosario</dc:creator><dc:title>Clinical parameters predicted the progression to dementia in oldest old patients with mild cognitive impairment (MCI)</dc:title><dc:identifier>ART-2025-145439</dc:identifier><dc:description>Background: This study intends to assess to what extent instruments commonly used in clinical practice, as well as plasma p-tau-181, can predict the progression from MCI to dementia. The usefulness of a disease progression model (DPM) is also explored.
Methods: A longitudinal, prospective nested case-control study was conducted with patients from the Geriatrics outpatient clinics who met the MCI International Working Group criteria. The patients had a first clinical interview and two follow-ups after 12 and 24 months. Validated Spanish instruments were used for assessment, including the Mini-Mental State Examination (MMSE), the clock test, verbal fluency, the EURO-D depression scale, Barthel’s Index, and Lawton’s Index. P-tau-181 analysis was performed with SIMOA (Single MOlecule Array). A robust parametric disease progression model (RPDPM) was developed.
Results. Fifty-nine patients fulfilled the inclusion criteria. The median age was 82.7 + /−8.7 years, 93 % had amnestic MCI and 45.8 % progressed to dementia (ICD-11 criteria) in two years. P-tau-181 was not prognostic. An RPDPM with the MMSE, clock test, and Lawton’s Index could predict progression to dementia with an AUC of 0.945.
Conclusion: A combination of the MMSE, clock test, and Lawton’s Index in a DPM model predicted progression from MCI to dementia best. P-tau and other blood biomarkers did not predict progression. Our results highlight the strength of clinical variables to predict the progression of MCI.</dc:description><dc:date>2025</dc:date><dc:source>http://zaguan.unizar.es/record/162920</dc:source><dc:doi>10.1016/j.inpsyc.2025.100129</dc:doi><dc:identifier>http://zaguan.unizar.es/record/162920</dc:identifier><dc:identifier>oai:zaguan.unizar.es:162920</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/A19-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/FIS/PI21-00286</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/FEDER/PI21-00372</dc:relation><dc:identifier.citation>International Psychogeriatrics (2025), 100129 [8 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>https://creativecommons.org/licenses/by/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>