Evidence map›Paper›PMID 41234527›Full record

ArticleBrain communications2025

Microstructural grey matter alterations in patients with behavioural variant frontotemporal dementia.

Behnaz Akbarian, Kilian Hett, Tony Phan, Jayden J Lee, James Eaton, Manus J Donahue, R Ryan Darby

Abstract read
In one paragraph

Article in Brain communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Behnaz AkbarianDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID https://orcid.org/0000-0002-2016-8201
Kilian HettDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID https://orcid.org/0000-0001-8831-4247
Tony PhanDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Jayden J LeeDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID https://orcid.org/0000-0002-3611-4187
James EatonDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Manus J DonahueDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
R Ryan DarbyDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID https://orcid.org/0000-0003-0326-1268

Funding

Antisocial Behavior in Frontotemporal Dementia: Behavioral Phenotypes, Neural Markers, and Decision-Making MechanismsR01AG081655 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Richard Ryan Darby · 2024 to 2026
$2.5M
Cognitive and Neural Mechanisms of Antisocial Behavior in Frontotemporal DementiaK23AG070320 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DARBY, RICHARD RYAN · 2021 to 2025
$857k
NIA NIH HHS K23 AG070320NIA NIH HHS R01 AG081655
6 · The paper itself

Abstract

Behavioural variant frontotemporal dementia is characterized by progressive changes to personality and behaviour, yet early detection and disease staging remain challenging. Current clinical neuroimaging relies on visual assessment of atrophy patterns, which may overlook subtle structural changes. While volumetric analysis has improved the ability to detect neurodegeneration and track disease progression, it may lack the sensitivity to identify microstructural alterations that precede frank atrophy. Texture analysis, a quantitative approach that evaluates the spatial regularity of grey matter density, has demonstrated promise in detecting early microstructural changes in Alzheimer's disease and distinguishing frontotemporal dementia subtypes. However, its potential as a biomarker for early behavioural variant frontotemporal dementia detection and disease staging remain unexplored. This study evaluates the potential of autocorrelation-based texture features as biomarkers for detecting early-stage behavioural variant frontotemporal dementia and tracking disease progression, comparing their sensitivity and specificity to regional brain volume. We analysed structural MRI scans from behavioural variant frontotemporal dementia patients with mild (

Indexed as

brain volumedisease progressionearly diagnosisfrontotemporal dementiatexture analysis

Identifiers

PMID41234527
PMCPMC12609174

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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 OpenQuestion graph.