Evidence map›Paper›PMID 37855956›Full record

ArticleBrain imaging and behavior2024

Fronto-striatal alterations correlate with apathy severity in behavioral variant frontotemporal dementia.

Neeraj Upadhyay, Annika Spottke, Anja Schneider, Daniel C Hoffmann, Ingo Frommann, Tommaso Ballarini, Klaus Fliessbach, Benjamin Bender, Hauke R Heekeren, John Dylan Haynes and 18 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Brain imaging and behavior, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Depression and apathy in frontotemporal dementia: a short assessment of facts and outlook.Journal of neural transmission (Vienna, Austria : 1996) · 2026
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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

28 authors at 10 institutions in 1 country.

Neeraj UpadhyayDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany. Neeraj.upadhyay@ukbonn.de.
Annika SpottkeDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Anja SchneiderDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Daniel C HoffmannDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Ingo FrommannDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Tommaso BallariniDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Klaus FliessbachDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Benjamin BenderDepartment of Diagnostic and Interventional Neuroradiology, University of Tuebingen, Tuebingen, Germany.
Hauke R HeekerenDepartment of Education and Psychology, Freie Universität Berlin, Berlin, Germany.
John Dylan HaynesBernstein Center for Computational Neuroscience, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Michael EwersDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Munich, Germany.
Emrah DüzelDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Magdeburg, Germany.
Wenzel GlanzDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Magdeburg, Germany.
Laura DobischDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Magdeburg, Germany.
Katharina BuergerDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Munich, Germany.
Daniel JanowitzInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Munich, Germany.
Johannes LevinDepartment of Neurology, University Hospital of Munich, Ludwig-Maximilians-Universität (LMU) Munich, Munich, Germany.
Adrian DanekDepartment of Neurology, University Hospital of Munich, Ludwig-Maximilians-Universität (LMU) Munich, Munich, Germany.
Stefan TeipelDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Rostock, Germany.
Ingo KilimannDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Rostock, Germany.
Matthis SynofzikDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Tübingen, Germany.
Carlo WilkeDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Tübingen, Germany.
Oliver PetersDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Berlin, Germany.
Lukas PreisDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Berlin, Germany.
Josef PrillerDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Berlin, Germany.
Eike Jakob SpruthDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Berlin, Germany.
Frank JessenDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
Henning BoeckerDeutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany.
German Center for Neurodegenerative Diseases · DEUniversity Hospital Bonn · DELMU Klinikum · DELudwig-Maximilians-Universität München · DEBernstein Center for Computational Neuroscience Berlin · DECologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEEinstein Center for Neurosciences Berlin · DEKlinikum rechts der Isar · DEUniversity of Rostock · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Structural and functional changes in cortical and subcortical regions have been reported in behavioral variant frontotemporal dementia (bvFTD), however, a multimodal approach may provide deeper insights into the neural correlates of neuropsychiatric symptoms. In this multicenter study, we measured cortical thickness (CTh) and subcortical volumes to identify structural abnormalities in 37 bvFTD patients, and 37 age- and sex-matched healthy controls. For seed regions with significant structural changes, whole-brain functional connectivity (FC) was examined in a sub-cohort of N = 22 bvFTD and N = 22 matched control subjects to detect complementary alterations in brain network organization. To explore the functional significance of the observed structural and functional deviations, correlations with clinical and neuropsychological outcomes were tested where available. Significantly decreased CTh was observed in the bvFTD group in caudal middle frontal gyrus, left pars opercularis, bilateral superior frontal and bilateral middle temporal gyrus along with subcortical volume reductions in bilateral basal ganglia, thalamus, hippocampus, and amygdala. Resting-state functional magnetic resonance imaging showed decreased FC in bvFTD between: dorsal striatum and left caudal middle frontal gyrus; putamen and fronto-parietal regions; pallidum and cerebellum. Conversely, bvFTD showed increased FC between: left middle temporal gyrus and paracingulate gyrus; caudate nucleus and insula; amygdala and parahippocampal gyrus. Additionally, cortical thickness in caudal, lateral and superior frontal regions as well as caudate nucleus volume correlated negatively with apathy severity scores of the Neuropsychiatry Inventory Questionnaire. In conclusion, multimodal structural and functional imaging indicates that fronto-striatal regions have a considerable influence on the severity of apathy in bvFTD.

Indexed as

ApathyFrontotemporal DementiaBrainGray MatterHumansMagnetic Resonance ImagingBehavioral variant FTDCortical thicknessExecutive dysfunctionNeuropsychiatric inventory questionnaire for apathy and disinhibitionResting state functional connectivity

Identifiers

PMID37855956
PMCPMC10844138
OpenAlexW4387765515

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.