Evidence map›Paper›PMID 31795051›Full record

ArticleNeuroImage. Clinical2019

Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia.

Ana L Manera, Mahsa Dadar, D Louis Collins, Simon Ducharme, Frontotemporal Lobar Degeneration Neuroimaging Initiative

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.4field-weighted citation impact, top 3% of its field
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

32 citing papers in PubMed, 74 citations in OpenAlex.

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  4. Assessing the role of volumetric brain information in multiple sclerosis progression.Computational and structural biotechnology journal · 2025
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  5. Review
  6. Deformation-based morphometry: a sensitive imaging approach to detect radiation-induced brain injury?Cancer imaging : the official publication of the International Cancer Imaging Society · 2024
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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

5 authors at 1 institution in 1 country.

Ana L ManeraMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801, University, Montreal, Quebec H3A 2B4, Canada.
Mahsa DadarMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801, University, Montreal, Quebec H3A 2B4, Canada.
D Louis CollinsMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801, University, Montreal, Quebec H3A 2B4, Canada. Electronic address: louis.collins@mcgill.ca.
Simon DucharmeMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801, University, Montreal, Quebec H3A 2B4, Canada; Department of Psychiatry, McGill University Health Centre, Montreal Canada.
Frontotemporal Lobar Degeneration Neuroimaging Initiative
Montreal Neurological Institute and Hospital · CA

Funding

The Frontotemporal Lobar Degeneration Neuroimaging InitiativeR01AG032306 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, HOWARD J · 2009 to 2013
$10.0M
NIA NIH HHS R01 AG032306
6 · The paper itself

Abstract

objectiveTo objectively quantify how cerebral volume loss could assist with clinical diagnosis and clinical trial design in the behavioural variant of frontotemporal dementia (bvFTD).

methodsWe applied deformation-based morphometric analyses with robust registration to precisely quantify the magnitude and pattern of atrophy in patients with bvFTD as compared to cognitively normal controls (CNCs), to assess the progression of atrophy over one year follow up and to generate clinical trial sample size estimates to detect differences for the structures most sensitive to change. This study included 203 subjects - 70 bvFTD and 133 CNCs - with a total of 482 timepoints from the Frontotemporal Lobar Degeneration Neuroimaging Initiative.

resultsDeformation based morphometry (DBM) revealed significant atrophy in the frontal lobes, insula, medial and anterior temporal regions bilaterally in bvFTD subjects compared to controls with outstanding subcortical involvement. We provide detailed information on regional changes per year. In both cross-sectional analysis and over a one-year follow-up period, ventricle expansion was the most prominent differentiator of bvFTD from controls and a sensitive marker of disease progression.

conclusionsAutomated measurement of ventricular expansion is a sensitive and reliable marker of disease progression in bvFTD to be used in clinical trials for potential disease modifying drugs, as well as possibly to implement in clinical practice. Ventricular expansion measured with DBM provides the lowest published estimated sample size for clinical trial design to detect significant differences over one and two years.

Indexed as

AgedAtrophyBrainCase-Control StudiesCerebral VentriclesCorpus CallosumDisease ProgressionFemaleFrontal LobeFrontotemporal DementiaGyrus CinguliHumansImage Processing, Computer-AssistedLongitudinal StudiesMagnetic Resonance ImagingMaleDeformation based morphometryDiagnostic biomarkerFrontotemporal dementiaMagnetic resonance imagingMorphometric analysis

Identifiers

PMID31795051
PMCPMC6879994
OpenAlexW2985780005

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.