1. The Latin American Spanish version of the Face-Name Associative Memory Exam is sensitive to cognitive and pathological changes in preclinical autosomal dominant Alzheimer's disease.
- Author
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Vila-Castelar, Clara, Muñoz, Nathalia, Papp, Kathryn V., Amariglio, Rebecca E., Baena, Ana, Guzmán-Vélez, Edmarie, Bocanegra, Yamile, Sanchez, Justin S., Reiman, Eric M., Johnson, Keith A., Sperling, Reisa A., Lopera, Francisco, Rentz, Dorene M., and Quiroz, Yakeel T.
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ALZHEIMER'S disease , *APOLIPOPROTEIN E4 , *POSITRON emission tomography , *CEREBRAL amyloid angiopathy , *NEUROPSYCHOLOGICAL tests , *ASSOCIATIVE memory (Psychology) , *PET therapy , *RANK correlation (Statistics) - Abstract
Background: To determine whether performance on the Latin American Spanish version of the Face-Name Associative Memory Exam (LAS-FNAME) can differentiate between cognitively intact carriers of an autosomal dominant Alzheimer's disease mutation (E280A) in Presenilin-1, who are genetically determined to develop early-onset dementia, from matched non-carriers. We also sought to examine whether LAS-FNAME performance is associated with amyloid-β and regional tau burden in mutation carriers. Methods: A total of 35 cognitively intact mutation carriers (age range 26–41), 19 symptomatic carriers, and 48 matched non-carriers (age range 27–44) completed a neuropsychological assessment including the LAS-FNAME. A subset of participants (31 carriers [12 symptomatic] and 35 non-carriers) traveled from Colombia to Boston to undergo positron emission tomography (PET) using Pittsburgh compound B to measure mean cortical amyloid-β and flortaucipir for regional tau. ANOVA analyses and Spearman correlations were used to examine group differences and relationships among LAS-FNAME performance and amyloid-β and tau accumulation. Results: Compared to non-carriers, cognitively intact mutation carriers had lower scores on the LAS-FNAME Total Scores (p =.040). Across all carriers (including symptomatic carriers), higher levels of amyloid-β (r = −.436, p =.018) and regional tau in the entorhinal (r = −.394, p =.031) and inferior temporal cortex (r = −.563, p =.001) were associated with lower LAS-FNAME Total Scores. Conclusions: Performance on the LAS-FNAME differentiated between cognitively intact mutation carriers from non-carriers and was associated with greater amyloid and tau burden when examining all carriers. Findings suggest that the LAS-FNAME is sensitive to early clinical and pathological changes and can potentially help track disease progression in Spanish-speaking individuals. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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