CU PET Aβ and Tau Positive Individuals Show Impairment in MoCA Delayed Recall

Abstract Background Identification of cognitively unimpaired (CU) individuals who may progress to mild cognitive impairment (MCI), is a pressing issue in the Alzheimer’s disease (AD) field, since therapeutic interventions may be more effective in the absence of cognitive impairment and neurodegeneration. CU individuals positive for amyloid and tau PET are very likely in the AD pathway. In out‐patient cognitive screening, we use rapid and simple tests such as The Montreal Cognitive Assessment (MoCA) ‐ a composite of executive, visuospatial, naming, attention, language, abstraction, delayed recall, and orientation performances. We hypothesize that sub‐categorizing the CU group based on the presence of amyloid (A) and tau (T) pathologies, as measured by PET, can reveal subtle cognitive deficits, even in a clinical test with low sensitivity such as MoCA. Method We included 88 CU [defined as CDR global score of 0] older adults with available head‐to‐head MK6240 tau‐PET and Flortaucipir tracers from the ongoing HEAD multi‐site observational study. They also underwent Amyloid PET imaging using PiB or NAV4694. MoCA testing was done around the imaging time. To increase similarity with clinical practice, Amyloid and Tau PET positivity was defined using visual reads. Based on tracer uptake status, we categorized the individuals into A‐T‐, A‐T+, A+T‐ and A‐T‐ groups. Unpaired t‐test and one‐way ANOVA were used to test for significant differences between groups. Result 2‐tailed p‐values were significant between the A‐T‐ group and the A+T+ group for MoCA total score [p: 0.0025 and p: 0.0025]. When we stratified MoCA in the different cognitive domains, we found that the results were driven by MoCA (memory) Delayed Recall score [p: 0.0007 and p: 0.0162]. A‐T+ vs A+T+ was also significant [p: 0.0099] for MoCA Delayed Recall. Both tau tracers (MK6240 and Flortaucipir) showed similar performance for determining T+ and identifying cognitive decline. Conclusion MoCA, a simple and commonly administered in‐office neuropsychological test, can detect subtle cognitive dysfunction in CU older adults who are Aß and tau positive (A+/T+). These CU A+/T+ individuals are likely on the path to developing AD dementia.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.094075
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
0.00
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article

CU PET Aβ and Tau Positive Individuals Show Impairment in MoCA Delayed Recall

Val J. Lowe, Dana Tudorascu, Peter Charles Lemaire, Tharick Ali Pascoal et al.
Alzheimer s & Dementia
Dementia and Cognitive Impairment Research
article

CU PET Aβ and Tau Positive Individuals Show Impairment in MoCA Delayed Recall

Val J. Lowe, Dana Tudorascu, Peter Charles Lemaire, Tharick Ali Pascoal, Marina Scop Medeiros, Cynthia Felix, Guilherme Povala, Belén Pascual, Carolina Soares, William E. Klunk, Guilherme Bauer‐Negrini, Pâmela C.L. Ferreira, Matheus Scarpatto Rodrigues, Beth E. Snitz, Bruna Bellaver, George W. Rebok, David N. Soleimani‐Meigooni, Sarah Abbas, Suzanne L. Baker, Firoza Zubeida Lussier, Cristiano Schaffer Aguzzoli, Lívia Amaral, Brian A. Gordon, Pedro Rosa‐Neto, William J. Jagust, Markley S. Oliveira, Hwamee Oh, Felix Joy Kollasserry
article en

Abstract

Abstract Background Identification of cognitively unimpaired (CU) individuals who may progress to mild cognitive impairment (MCI), is a pressing issue in the Alzheimer’s disease (AD) field, since therapeutic interventions may be more effective in the absence of cognitive impairment and neurodegeneration. CU individuals positive for amyloid and tau PET are very likely in the AD pathway. In out‐patient cognitive screening, we use rapid and simple tests such as The Montreal Cognitive Assessment (MoCA) ‐ a composite of executive, visuospatial, naming, attention, language, abstraction, delayed recall, and orientation performances. We hypothesize that sub‐categorizing the CU group based on the presence of amyloid (A) and tau (T) pathologies, as measured by PET, can reveal subtle cognitive deficits, even in a clinical test with low sensitivity such as MoCA. Method We included 88 CU [defined as CDR global score of 0] older adults with available head‐to‐head MK6240 tau‐PET and Flortaucipir tracers from the ongoing HEAD multi‐site observational study. They also underwent Amyloid PET imaging using PiB or NAV4694. MoCA testing was done around the imaging time. To increase similarity with clinical practice, Amyloid and Tau PET positivity was defined using visual reads. Based on tracer uptake status, we categorized the individuals into A‐T‐, A‐T+, A+T‐ and A‐T‐ groups. Unpaired t‐test and one‐way ANOVA were used to test for significant differences between groups. Result 2‐tailed p‐values were significant between the A‐T‐ group and the A+T+ group for MoCA total score [p: 0.0025 and p: 0.0025]. When we stratified MoCA in the different cognitive domains, we found that the results were driven by MoCA (memory) Delayed Recall score [p: 0.0007 and p: 0.0162]. A‐T+ vs A+T+ was also significant [p: 0.0099] for MoCA Delayed Recall. Both tau tracers (MK6240 and Flortaucipir) showed similar performance for determining T+ and identifying cognitive decline. Conclusion MoCA, a simple and commonly administered in‐office neuropsychological test, can detect subtle cognitive dysfunction in CU older adults who are Aß and tau positive (A+/T+). These CU A+/T+ individuals are likely on the path to developing AD dementia.

Alzheimer s & DementiaVol. 20(S9)
Houston Methodist (US), Johns Hopkins University (US), Lawrence Berkeley National Laboratory (US), University of Pittsburgh (US), Washington University in St. Louis (US), Brown University (US), McGill University Health Centre (CA), Alzheimer’s Disease Neuroimaging Initiative (US), Mayo Clinic in Arizona (US), Global Brain Health Institute (US), Indian Statistical Institute (IN)
Openalex Percentile: Top 65%
Dementia and Cognitive Impairment Research
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