Evidence map›Paper›PMID 40878813›Full record

ArticleArchives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists2025

Can Frontal Assessment Battery Discriminate between Patients with Alzheimer's and Frontotemporal Dementia?

Fabrissio Grandi, Loreto Olavarría, Mario A Parra, David Martínez-Pernía, Cesar Serey, Jose Lema, Carolina Delgado, Teresita Ramos, Patricia Lillo, Adolfo M García and 2 more

Abstract read
In one paragraph

Article in Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Fabrissio GrandiGeroscience Center for Brain Health and Metabolism (GERO), Faculty of Medicine, University of Chile, Santiago, Metropolitan Region, 7750162, Chile.ORCID 0000-0001-6196-8072
Loreto OlavarríaGeroscience Center for Brain Health and Metabolism (GERO), Faculty of Medicine, University of Chile, Santiago, Metropolitan Region, 7750162, Chile.ORCID 0000-0003-0217-041X
Mario A ParraDepartment of Psychological Sciences and Health, University of Strathclyde, Glasgow G1 1QE, UK.ORCID 0000-0002-2412-648X
David Martínez-PerníaGeroscience Center for Brain Health and Metabolism (GERO), Faculty of Medicine, University of Chile, Santiago, Metropolitan Region, 7750162, Chile.
Cesar SereyFaculty of Health Sciences and Social Sciences, Universidad de las Américas, Santiago, Metropolitan Region, 7550000, Chile.
Jose LemaGeroscience Center for Brain Health and Metabolism (GERO), Faculty of Medicine, University of Chile, Santiago, Metropolitan Region, 7750162, Chile.
Carolina DelgadoDepartment of Neuroscience, Faculty of Medicine, Universidad de Chile, Santiago, Metropolitan Region, 8380453, Chile.ORCID 0000-0001-5551-0065
Teresita RamosMemory Unit, Memory and Neuropsychiatric Center (CMYN), Faculty of Medicine, Neurology Department, Hospital del Salvador, Universidad de Chile, Santiago, Metropolitan Region, 8420000, Chile.
Patricia LilloGeroscience Center for Brain Health and Metabolism (GERO), Faculty of Medicine, University of Chile, Santiago, Metropolitan Region, 7750162, Chile.
Adolfo M GarcíaCognitive Neuroscience Center, Universidad de San Andrés, Buenos Aires, Buenos Aires Province, C1426BCE, Argentina.
Graciela Muniz-TerreraHeritage College of Ostheopatic Medicine, Ohio University, Athens, OH 45701, USA.
Andrea SlachevskyGeroscience Center for Brain Health and Metabolism (GERO), Faculty of Medicine, University of Chile, Santiago, Metropolitan Region, 7750162, Chile.ORCID 0000-0001-6285-3189

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
An automated machine learning approach to language changes in Alzheimer’s disease and frontotemporal dementia across Latino and English-speaking populationsR01AG075775 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI, Adolfo Martin Garcia · 2023 to 2026
$7.2M
US-South American Initiative for Genetic-Neural-Behavioral Interactions in Human Neurodegenerative ResearchR01AG057234 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Claudia Duran-Aniotz, Agustin M. Ibanez · 2019 to 2026
$6.1M
Circadian Disturbance and Dementia in Latin AmericaR01AG083799 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Kun Hu, Agustin M. Ibanez · 2023 to 2026
$3.0M
Agencia Nacional de Promoción Científica y Tecnológica 01-PICTE-2022-05-00103ANID 1250091ANID 1250317Bluefield Project to Cure Frontotemporal DementiaDICYT-USACH 032351GDASFogarty International Center and the National Institutes of HealthGlobal Brain Health InstituteMulti-partner Consortium to Expand Dementia Research in Latin AmericaNIA NIH HHS P01 AG019724NIA NIH HHS R01 AG057234NIA NIH HHS R01AG057234NIA NIH HHS R01 AG075775NIA NIH HHS R01AG075775NIA NIH HHS R01 AG083799NIA NIH HHS R01AG21051NIH HHS 2P01AG019724NIH HHS R01AG075775NIH HHS R01AG083799
6 · The paper itself

Abstract

objectivesThe Frontal Assessment Battery (FAB) is a widely used tool for assessing executive function. However, its ability to distinguish between Alzheimer's disease dementia (ADD) and behavioural variant frontotemporal dementia (bvFTD) remains under debate. This study assessed the diagnostic utility of the Chilean version of the FAB (FAB-Ch) in differentiating ADD from bvFTD and used data-driven cluster analysis to explore dysexecutive profiles.

methodA total of 288 participants were recruited: 45 with ADD, 33 with bvFTD, and 208 cognitively unimpaired controls (CU). Mean FAB-Ch total scores were compared across groups. Receiver operating characteristic (ROC) curves evaluated the instrument's ability to distinguish (i) dementia from no dementia, (ii) ADD from bvFTD, and (iii) executive dysfunction. Hierarchical cluster analysis was conducted to identify executive profiles among dementia patients.

resultsFAB-Ch scores were significantly lower in individuals with dementia compared to controls (p < .001). However, there were no significant differences between ADD and bvFTD groups (p = .59). The FAB-Ch showed strong discriminatory power between dementia and controls (AUC = 0.882; sensitivity = 0.731; specificity = 0.885), but poor discrimination between ADD and bvFTD (AUC = 0.465; p = .59). Cluster analysis among patients with dementia revealed three distinct executive profiles corresponding to different levels of cognitive impairment (p < .001).

conclusionThe FAB-Ch effectively differentiates individuals with dementia from cognitively unimpaired controls but does not distinguish between ADD and bvFTD. Nevertheless, it is sensitive to executive dysfunction and can aid in the clinical characterization of dementia severity and heterogeneity.

Indexed as

Alzheimer DiseaseExecutive FunctionFrontotemporal DementiaNeuropsychological TestsAgedCluster AnalysisDiagnosis, DifferentialFemaleFrontal LobeHumansMaleMiddle AgedROC CurveAlzheimer’s disease dementiaBehavioral variant frontotemporal dementiadementiaexecutive dysfunctionFrontal assessment battery

Identifiers

PMID40878813
PMCPMC12644060

What Socratic holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.