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

被引:10
|
作者
Vila-Castelar, Clara [1 ]
Munoz, Nathalia [1 ]
Papp, Kathryn V. [2 ,3 ]
Amariglio, Rebecca E. [2 ,3 ]
Baena, Ana [4 ]
Guzman-Velez, Edmarie [1 ]
Bocanegra, Yamile [4 ]
Sanchez, Justin S. [3 ]
Reiman, Eric M. [5 ]
Johnson, Keith A. [2 ,6 ]
Sperling, Reisa A. [2 ,3 ,7 ]
Lopera, Francisco [4 ]
Rentz, Dorene M. [2 ,3 ]
Quiroz, Yakeel T. [1 ,3 ,4 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02115 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Dept Neurol, Boston, MA 02115 USA
[3] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02115 USA
[4] Univ Antioquia, Grp Neurociencias Antioquia, Medellin, Colombia
[5] Banner Alzheimers Inst, Phoenix, AZ USA
[6] Harvard Med Sch, Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02115 USA
[7] Harvard Med Sch, Massachusetts Gen Hosp, Athinoula Martinos Ctr Biomed Imaging, Charlestown, MA USA
关键词
Alzheimer's disease; Autosomal dominant Alzheimer's disease; Neuropsychology; Associative memory; Imaging; PET; AMYLOID BURDEN; TAU; PET; BETA;
D O I
10.1186/s13195-020-00671-w
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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-beta 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-beta and flortaucipir for regional tau. ANOVA analyses and Spearman correlations were used to examine group differences and relationships among LAS-FNAME performance and amyloid-beta 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-beta (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.
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页数:11
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