LAM test: a new cognitive marker for early detection in preclinical Alzheimer's disease
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Identificadores
URI: https://hdl.handle.net/10902/36333DOI: 10.3233/JAD-240067
ISSN: 1387-2877
ISSN: 1875-8908
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García Martínez, María; Pozueta Cantudo, Ana; Lage Martínez, Carmen; Martínez Dubarbie, Francisco; López García, Sara; Fernández Matarrubia, Marta; Corrales Pardo, Andrea





Fecha
2024-07Derechos
© IOS Press. The final publication is available at IOS Press through https://doi.org/10.3233/JAD-240067
Publicado en
Journal of Alzheimer's Disease, 2024, 100(3), 1039-1053
Editorial
IOS Press
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Palabras clave
Alzheimer’s disease
Associative memory
Cognitive markers
Early detection
Long-term forgetting
Neuropsychological assessment
Preclinical Alzheimer’s disease
Resumen/Abstract
Background: With the arrival of disease-modifying treatments, it is mandatory to find new cognitive markers that are sensitive to Alzheimer's disease (AD) pathology in preclinical stages.
Objective: To determine the utility of a newly developed Learning and Associative Memory face test: LAM test. This study examined the relationship between AD cerebrospinal fluid (CSF) biomarkers and performance on LAM test, and assessed its potential clinical applicability to detect subtle changes in cognitively healthy subjects at risk for AD.
Methods: We studied eighty cognitively healthy volunteers from the Valdecilla cohort. 61% were women and the mean age was 67.34 years (±6.416). All participants underwent a lumbar puncture for determination of CSF biomarkers and an extensive neuropsychological assessment, including performance on learning and associative memory indices of the LAM-test after 30 min and after 1 week, and two classic word lists to assess verbal episodic memory: the Rey Auditory Verbal Learning Test (RAVLT) and the Free and Cued Selective Reminding Test (FCSRT). We analyzed cognitive performance according to amyloid status (A+ versus A-) and to ATN model (A-T-N-; A+T-N-; A+T+N-/A+T+N+).
Results: Performance on the LAM-test was significantly correlated with CSF Aβ ratio. A+ participants performed worse on both learning (mean difference = 2.19, p = 0.002) and memory LAM measures than A- (mean difference = 2.19, p = 0.004). A decline in performance was observed along the Alzheimer's continuum, with significant differences between ATN groups.
Conclusions: Our findings suggest that LAM test could be a useful tool for the early detection of subjects within the AD continuum, outperforming classical memory tests.
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